Omics: The way forward to enhance abiotic stress tolerance in Brassica napus L

ABSTRACT Plant abiotic stresses negative affects growth and development, causing a massive reduction in global agricultural production. Rapeseed (Brassica napus L.) is a major oilseed crop because of its economic value and oilseed production. However, its productivity has been reduced by many environmental adversities. Therefore, it is a prime need to grow rapeseed cultivars, which can withstand numerous abiotic stresses. To understand the various molecular and cellular mechanisms underlying the abiotic stress tolerance and improvement in rapeseed, omics approaches have been extensively employed in recent years. This review summarized the recent advancement in genomics, transcriptomics, proteomics, metabolomics, and their imploration in abiotic stress regulation in rapeseed. Some persisting bottlenecks have been highlighted, demanding proper attention to fully explore the omics tools. Further, the potential prospects of the CRISPR/Cas9 system for genome editing to assist molecular breeding in developing abiotic stress-tolerant rapeseed genotypes have also been explained. In short, the combination of integrated omics, genome editing, and speed breeding can alter rapeseed production worldwide.


Introduction
As agriculture greatly depends on the prevailing atmosphere, the crop plants often suffer from various environmental or abiotic stress due to climate change. There are many abiotic stresses, viz. salinity, drought, cold, waterlogging, and temperature fluctuations, which considerably hinder the growth rate and reduce agricultural yield globally. 1,2 As reported by USDA-FAO, drought and salt stress are important limiting components affecting about 26% and 20% of the agricultural land, respectively (American Geophysical Union; https://sites. agu.org). Soil salinity is the second major limiting factor of agriculture. Salt stress mostly affects the agricultural land of arid and semi-arid regions worldwide. 3 Plants under dehydration-inducing conditions ultimately hinder the growth rate, decrease crop production, and encourage adverse effects on plant physiological, metabolic, and biochemical processes. [2][3][4] Moreover, the effect of several other abiotic stresses such as waterlogging, 5,6 extreme temperature, 7 and metals/metalloids toxicity on crop productivity have also been reported in different crops, including rapeseed. 8 Brassica napus L., also called rapeseed or canola, has emerged as an important crop globally through rigorous breeding programs during the past few decades. Among oilseed crops, rapeseed is second in world oilseed production only to soybean. It belongs to the Brassicaceae family, that have 419 genera and 4130 species worldwide. Rapeseed genome is 2 n = 38 (AACC), which arises from the genome hybridization of B. oleracea and B. rapa ( Fig. 1; See refs. 14, 15) Rapeseed is now primarily grown in China, Canada, Europe as a cause of edible oil, livestock ration, and industrial derivatives. 16,17 Rapeseed oil content is about 30.6-48.3% of the dry weight. The oil profile of rapeseed includes vital fatty acids such as oleic (56.80-64.92%), palmitic (4.18--5.01%), linoleic (17.11-20.92%) acids. The quantity of α-tocopherol is about 13.22-40.01% of the total oil contents. 18 Due to climate change, urbanization and industrialization, abiotic stresses have become the main threat to crop production. Rapeseed, along with major crops worldwide, is frequently subjected to stresses which have significant effects on the physiological, biochemical, and molecular functions of plants, which ultimately impacting crop growth and production. 8 Improved abiotic stress tolerance of rapeseed is a fundamental approach to increase oilseed production. 19,20 General stress signaling pathways are described in Fig. 2.
Over the past decade, several reports indicated cloning and overexpression of the genes in rapeseed which enables plants to withstand several abiotic stresses (Table 1). Earlier, the BnNAC485 gene related to the NAC family was cloned, and results show that BnNAC485 was significantly expressed in 21-day-old seedling and cotyledon that was prompted by abiotic stresses. 28 In another study, the overexpression of BnNCED3 increases abscisic acid (ABA) accumulation, nitric oxides (NO), and generation of reactive oxygen species (ROS) in transgenic rapeseed. Furthermore, transgenic lines displayed restricted seed growth, lateral root initiation, and improvement of ABA-mediated leaf senescence by modulating ABA synthesis. 43 Cloning and expression scrutiny of BnICE1 revealed that BnICE1 is vigorously linked with cold stress tolerance, particularly at low temperatures. 21 Regulation and molecular characterization of the C-repeat-binding factor (CBF) exposed that CBF was closely connected with cold stress. 44 Recently, the identification and expression analysis of BnBADH1 increases salinity and drought stress tolerance, 37 and so on. Further examples of rapeseed abiotic stress-related genes are presented in Table 1.
The improvement of Brassica spp. for abiotic stress tolerance has been addressed since a few decades, and several tools have been employed, such as identifying and manipulating crops for abiotic stress tolerance, applications of several omics tools for the elucidation of genes associated with abiotic stress tolerance. 45 However, the major discoveries in this arena are gene discovery in response to different stress, marker development, gene mapping, transcriptomic analysis, and regulation of physiological and biosynthetic mechanisms.
The advancement of omics tools such as genomics, transcriptomics, proteomics, metabolomics, and phenomics has modernized molecular biology research. These allowed meticulous examination of connections between molecular machinery to assimilate genes, proteins, and many essential regulatory components, collectively organizing systematic molecular strategies. 46 The genome Figure 1. Systematic triangle of cross-breeding among economically important six Brassica species comprising three diploids (green) and three allotetraploids (orange) along with their estimated genome size. Letters (ABC) within the ovals denote the genomic symbols. N means the number of chromosomes. U's triangle was created according to Nagaharu (1935). 9 Genome size was retrieved from refs. [10][11][12][13][14] sequencing of Brassica crops has allowed more understanding of crop genetics and opens new avenues for crop improvement. Moreover, it has transformed molecular and functional genomics in Brassica cultivars. 47 Various transgenic rapeseed cultivars have been developed that allow more tolerance than conventional varieties. Advancement in emerging approaches for genome editing (GE) like CRISPR/Cas9 has helped explore plants' mechanism against stress responses. 48 This review described the integrated omics approaches that could efficiently enhance rapeseed production for global requirements and sustainable agriculture production. Early prevalence of stress sensing via receptors/sensors cascades the downstream stress response by ROS, CaM, and phytohormones. Signal extension and transduction by secondary messengers such as PKs, PPs, MAPKs, CDPKs, CBLs, and CIPKs signaling cause differential regulation of transcription factors (TFs) and stress-responsive genes. The regulation of such TFs and genes leads to the adjustment of physiological, biochemical, and molecular responses, thus, improving stress tolerance. Boxes on the left side, indicating the essential genes and TFs that act and protect plants under extreme environmental stresses. Blue, red and green text color in the gene-boxes showing that these genes or TFs works in different stresses. Adapted and slightly modified from Raza (2020a), 8 with permission from Springer Nature. Table 1. The overview of abiotic stress-responsive genes or/and transcription factors of rapeseed along with their key responses under stress environment.

The Interplay of Omics Approaches to Address Abiotic Stresses
Omics approaches have been applied to gain insight in all biological mechanisms occurring during abiotic stresses in crops (Fig. 3). Over the past few decades, omics strategies have been improved to develop stress-resistance cultivars. Hence, a paradigm shift has been brought in research by these omics strategies to tackle abiotic factors and open up new horizons for enhanced understanding of numerous features responsible for crop resistance. To combat abiotic stresses, plants adjust their omics profiles accordingly. 46 Therefore, the association of omics techniques will help to uncover candidate genes and their biosynthesis pathways in the future. Deciphering the association among omics approaches will potentially help us to illuminate molecular pathways that are actively controlled by abiotic stresses. Additionally, these combined tools will provide a comprehensive data set for biological system analysis. Step-wise presentation of OMICS approaches for studying abiotic stress responses. Ultimately, the integration of omics tools, primarily genomics (mainly singlecell/tissuespecific) leads toward the genetic improvement of rapeseed by modulating several agronomic traits such as environmental stress tolerance, yield, plant height, seed rate, flowering, photosynthesis, and respiration rate, root and shoot length, grain quality and yield, biomass production, etc.

Genomics Approaches: Provide Insights into Stress-associated Mechanisms
Genomics tools have gained enormous importance for the elucidation of desired genes related to abiotic stress tolerance. During the last few years, significant advancement has been achieved by the researchers in the functional genomics era to scan the genomes of many crop species. 49 Several genomics tools have been implemented in plant biology to explore the genomes of many crops for abiotic stress-tolerance, such as quantitative trait loci (QTL) mapping, which has emerged as a valuable technique to investigate the genetic diversity of crops. Moreover, up-gradation of QTL mapping and marker technology has allowed deciphering modern breeding approaches like marker-assisted selection (MAS) and single nucleotide polymorphism (SNPs). 47,50 High-throughput sequencing techniques, such as next-generation sequencing (NGS), have made it feasible to sequence an organism's whole genome. The integrated approach of genome-wide association studies (GWAS) and NGS technologies have provided remarkable opportunities to predict stress-related genes. 51 Nevertheless, the whole genome comprising genic and intergenic regions can form a particular scheme for plant development. The relationship between functional, comparative, and structural genomics is incredibly desirable for organic production. 49 New opportunities have been created by the recent improvements in crop genomics to develop abiotic stresstolerant crops. Moreover, the availability of genomics platforms for gene identification and trait examination in rapeseed, which have enormous capabilities for molecular breeding integrated with modern tools of breeding related to GE techniques. The accessibility of a reference genome to rapeseed permits the application of such technologies in rapeseed could be predicted to attain significant progress in the future. In the subsequent sections, we have discussed the recent progress in major genomics tools.

Marker-assisted Breeding
For breeding and crop improvement, powerful approaches like marker-assisted breeding (MAB) and MAS have been comprehensively used to map numerous desired genes in rapeseed. 47,50,52 Molecular markers linked with stress-responsive genes or QTLs can be recognized, which can be employed as a secondary choice principle to advance breeding proficiency via MAS. However, the practice of MAS for operating modest traits has been modernized in numerous rapeseed breeding programs. Thus, MAS for enlightening multifaceted traits appears to be at initial stages. 47,50,53 Furthermore, to exploit the genetic diversity in different crop plants, a high throughput strategy of genomic tools is used. Rapeseed, which has a comparatively low level of genetic diversity, several studies based on genome-wide MAS have been conducted to describe the genetic variability in rapeseed. 47,50,52 Nucleotide sequences of genes have been established using DNA markers, which offer fundamental knowledge to understand the genetic divergence of a species from primitive families and leading landraces that hold their genetic materials well preserved in gene databank for future applications. 47,52,54 DNA markers are applied to probe the genome to screen desired loci and transgenes by repeated selective events. Certain important traits were identified, where DNA markers have been applied for genetic mapping in rapeseed. 52 Numerous SNPs have been discovered in rapeseed using QTL mapping for desired traits. 55 Likewise, RAPD, AFLP, ISSR, and SSR have been used to find the genetic variability in rapeseed. [56][57][58][59] Detailed information will be presented in the subsequent sections (2.1.1.1-2.1.1.7) to highlight the efforts in rapeseed mapping using different approaches.

The contribution of RAPD markers.
PCRbased random amplified polymorphic DNA (RAPD) markers primarily comprised on random amplification of segments of polymorphic DNA. 60 Previously, several studies have been carried out using RAPD markers for rapeseed mapping for different traits. For example, a double haploid (DH) population resulting from the F 1 generation of the cross Apollo (black-seeded) x YN90-1016 (yellow-seeded) rapeseed was examined to detect molecular markers related to the yellow-seed trait. 61 An essential gene (pigment 1) lined by 8 RAPD markers was linked with the yellow seed coat color trait in the F 1 generation. This gene described 72% phenotypic difference in seed coat color. 61 Likewise, 62 examined the F 2 , BC 1, and F 1derived DH population for seed color using 810 RAPD and 512 AFLP markers. Out of these, 240 RAPD markers showed polymorphisms among the parents. Additionally, 4 RAPDs and 16 AFLP primer pairs displayed polymorphisms among the bulks, whereas only 2 RAPD and 8 AFLP markers were detected in the locality of the seed coat color. 62 Furthermore, a polymorphic marker linkage map conveying nine linkage groups (LGs) was created from F 2:3 populations of rapeseed [SLMO46 (winter type and cold-resistant) x Quantum (spring type and cold susceptible)] using 47 RAPD markers. 63 They identified one presumed QTL for winter survival elucidating only a 5% phenotypic difference. The QTL was located on LG6 is amid 670 and 650 bp sized RAPD markers with 4 cM distance from the 650 bp marker and had adverse conserving consequence. 63 In another study, a similar rapeseed population by 47 RAPD and 32 SSR markers, a linkage map conveying 14 LGs was prepared and presumed QTLs were identified on 3, 8, 9, and 10 LGs. These QTLs explained a 24% phenotypic difference in the freezing tolerance in the studied rapeseed population. 64 Besides, RAPD markers have been extensively used to evaluate genetic diversity and polymorphism between different rapeseed genotypes/lines/populations. 58-59-65-68

The contribution of AFLP markers.
Amplified fragment length polymorphism (AFLP) is a PCR-based technique in which a subgroup of constraint remains are selectively amplified with oligonucleotide primers opposite to sequences. It can also be applied to fresh and partly decade-old DNA. 69 Previously, the separation of the rapeseed Bnms3 gene (responsible for recessive genic male sterility) for evolving precise PCR markers for MAS and understanding this gene's crucial function has been investigated. Notably, the Bnms3 gene was labeled with seven AFLP markers; out of these, six AFLPs were recognized to be co-segregated with the target gene in a population of 115 individuals. 70 In another study, Brassica 60 K Infinium SNP array, AFLP, and SSR markers were used to make a highdensity genetic map in the DH rapeseed population (Zhang et al. 2014c). Using the genetic map, a novel QTL (qBEC-A3a) for boron deficiency was identified, and a similar map was then employed to identify different QTLs related to plant growth (36 QTLs with 6.14-46.27% phenotypic difference) and boron uptake (12 QTLs with >10% phenotypic difference). These findings provided vital QTLs suited for fine mapping and the actual markers for improving breeding productivity in rapeseed. 71 Moreover, Fan et al. (2015) 72 described the QTLs' mapping related to waterlogging and drought resistance in the DH rapeseed population's seedling stage via AFLP and SSR markers. Significant genetic diversity was detected in resynthesized rapeseed lines using AFLP markers compared to the gene pools of conventional spring and winter rapeseed genotypes. 73 In the next experiment, these authors correlated the genetic diversity with the heterotic yield in trial hybrids. 74 Later, the yield characters of 184 F 2:3 lines were accessed via AFLP and SSR markers. Results show that 73 markers were linked with 12 yield characters with an involvement rate of 3.54-15.88% and an average of 6.60%. The genetic distance was expressively associated to heterosis of F 1 trials via 66 markers related to yield character and suggesting that the correctness of yield and heterosis estimate reliant on QTLs linked with yield characters in rapeseed required to be upgraded. 75,76 On the other hand, AFLP markers have been extensively used to access the genetic diversity among different rapeseed genotypes/lines/populations. 56,58,77

The contribution of SSR markers.
Simple sequence repeats (SSRs) or microsatellites are short tandem repeated motifs of 1-6 nucleotides present in huge amounts and may fluctuate in the number of repetitions at a specified locus. These markers have numerous benefits over other markers, such as hereditary co-dominance. 78 The sum of freely accessible Brassica SSR primers is growing because of openly sponsored international enterprises (www.brassica.info). Nevertheless, compared to other imperative crop plant species, limited SSR markers are easily accessible, meaning few consensus maps have been described in DH rapeseed populations. 79 The publicly available set of vigorous, extremely polymorphic, mapped SSR markers covering the entire rapeseed genome have helped rapeseed genetics researchers in mapping and genome amalgamation. 80 During the past few years, significant progress has been made using SSR markers in integrating available and new genetic maps. Further, the QTL alignment, playing a crucial role in correlation of candidate genes with QTLs. For instance, using F 2:3 rapeseed populations, 64 several major QTLs were detected on 3, 8, 9, and 10 LGs with a phenotypic difference of 24% in freezing tolerance. SSR markers, together with Brassica 60 K Infinium SNP array, were used to make a high-density genetic map in the DH rapeseed population under boron deficiency. This resulted in 12 QTLs with >10% phenotypic difference for boron uptake and a novel QTL linked with the growth and boron deficiency (Zhang et al. 2014c). In rapeseed, 53 SSR markers were expressively linked with 3 phenolic sections, and 11 markers were connected with total phenolic acid contents. Out of these, only 4 SSR markers result from QTL for seed color by association mapping. 81 Additionally, 25 and 11 SSR markers are related to seed coat color and oil content, respectively. In contrast, only six SSR markers are connected to both oil content and coat color. 82 In a recent study, 36 SSR markers have been used to examine the variability between 41 rapeseed lines linked with drought tolerance QTLs. 83 Apart from the abovementioned traits, SSR markers have shown great potential in deciphering genetic diversity between rapeseed genotypes/lines/populations [58,84,85,86].

The contribution of ISSR markers.
The commonly used PCR-based markers such as RAPDs, AFLPs, and SSRs have some limitations like low reproducibility, high cost, and need flanking sequences. Therefore, inter simple sequence repeat (ISSR) is an updated method that incapacitates these limitations. This method combines numerous advantages of AFLP-and SSR-based investigations with the universality of RAPD. [86][87][88] Water-stressed rapeseed cultivars showed maximum discrepancy subsidized by ISSR markers went to relative water content (78%) at normal state, to root/shoot index (66%) at modest stress state and to root length (53%) at severe stress environment. 89 Recently, while studying drought tolerance signals and their relationship with ISSR markers in rapeseed genotypes, most of the ISSR markers were found to be linked with some of the drought tolerance indices. 90 ISSRs have been effectively employed in the genetic diversity studies at inter and intra definite levels in numerous plant species, including rapeseed. 89,91,92 Molecular mapping using ISSRs linked with QTLs or candidate genes is yet to be reported in rapeseed, while this has been achieved in some other crop plants.

The contribution of SCAR markers.
To lessen the difficulties that rise when consuming conventional markers such as RAPD, ISSR, IRAP, AFLP, SSR, etc., the sequence characterized amplified region (SCAR) marker was established. These markers can be derived from ISSR, IRAP, and RAPD markers. It signifies a particular, distinct genomic DNA part that was noticed in PCR extension with a pair of definite primers. [93][94][95] These markers have great potential in plant identification at inter-and intra-specific species or population level. 93,96,97 Previously, the linkage mapping using SCAR markers has been linked with 18-carbon fatty acids in rapeseed. Developed SCAR marker (L1L9) shows about 25% genetic difference for 18-carbon fatty acids in rapeseed. 98 Later, using AFLP, SCAR markers have been developed for the trait-specific gene. For instance, SCAR markers have been characterized to be linked with a dominant genic male sterility [suppressor gene (Rf)] in rapeseed by several researchers. [99][100][101] Additionally, SCAR markers have been associated with self-incompatibility in rapeseed and showed significant results at a polymorphic level compared to CAPS markers. 102 The above-mentioned markers were handy for improving different traits and accelerating MAS progression in rapeseed breeding plans. For cultivar fingerprinting, transposon insertion-SCAR markers have been characterized in rapeseed. These markers can be considered a vital tool in the reverse genetic scheme for separating novel genes in rapeseed. 103

The contribution of CAPS markers.
Cleaved amplified polymorphic sequences (CAPS) markers are PCR-amplifications of DNA remains with specific primers after the digestion of restriction enzymes and the harvests' isolation in an agarose gel. Practical CAPS markers can be established on a target gene's identified sequence to analyze its regulation, structure, purpose, and expression. These markers are closely connected with the target gene and are particularly supportive of MAS. 104,105 Earlier, SCAR and CAPS markers were developed and mapped to be associated with seed coat color gene in a resynthesized purely yellow rapeseed line obtained from the F 1 DH population using a genome-walking method. 106 In a recent study, the SCAR and CAPS markers were linked with Leptosphaeria maculans resistance gene Rlm6 in B. napus x B. juncea interspecific hybrids. Segregation of both markers related to the Rlm6 gene was established by using F 2 and F 3 progeny. Interestingly, the segregation of CAPS markers and phenotype for blackleg disease cruelty in the F 2 population had a Mendelian ratio of 3:1 in resilient vs vulnerable plants, respectively, suggesting that the genetic regulator of resistance was carried by a dominant gene. 107 In a MAS analysis of new high oleic and low linolenic winter rapeseed inbred lines, genotyping was completed for the assortment of homozygous lines via allele-specific CAPS markers and SNaPshot assay. Lastly, new high oleic and low linolenic winter rapeseed recombinant lines were obtained, ready to be used as a preliminary material in developing new varieties with high oil value than traditional types. 108 In another study, CAPS markers were used for the identification of two mutant alleles (BnaA.FAD2 gene) in rapeseed. Further, CAPS markers also provided relatively good results while detecting the heterozygosity in BnaA.FAD2 gene. 109 These examples indicate the importance of CAPS markers in MAS studies to identify and develop new breeding lines.

The contribution of SNPs.
Genomes of all the organisms consist of single base pairs sequences called SNPs. Rapidly decreasing DNA charges for re-sequencing and accessibility of a more advanced SNP platform for rapeseed open up new horizons for significantly more effective gene mining and genetic mapping. 47 More than 75% of detected SNPs were useful and could be exploited in modern molecular breeding schemes. 47,110 Likewise, SNP analysis was documented to study the heat stress on different rapeseed varieties under field conditions, and data were recorded from flowering to maturity phase for different agronomic traits. Association mapping (AM) for various agronomic traits was executed to detect heat-related QTLs. For these 37,269 SNP markers were employed and showed that several genes were strongly correlated with abiotic stress-tolerance in rapeseed. 111 Numerous examples are presented in Table 2 and the next section.

Evidence of QTL and GWAS Studies
A GWAS is a method employed in genetics investigation to associate definite genetic differences with particular traits in different individuals. It overwhelms numerous restrictions of traditional gene mapping (QTL) by providing advanced resolution, often to the gene level, and consuming trials from formerly investigated populations in which frequently happening genetic differences can be connected with a phenotypic difference. The start of high-density SNP typing permitted wholegenome examinations to recognize often insignificant haplotype hunks that are pointedly associated with quantitative traits. 119,120 For instance, Jian et al. 121 studied the recombinant inbred lines (RIL) population at the seedling stage under salt and drought stress for GWAS. Notably, 2795 SNPs were detected, and the analysis revealed that numerous minor-effect loci regulate the germination percentage of rapeseed, and the various gene is activated under drought or salinity stress. Furthermore, a GWAS experiment was performed  122 Genetic mapping of QTLs is the 1 st phase for discovering the genetic design of a trait and in executing MAS in plant breeding scheme. 123 Stress tolerance results from multiple responses/ mechanisms, assessment of these mechanisms and stress-related QTLs has assisted plant breeders in developing elite genotypes with stress-tolerance. Genetic investigations for the development of abiotic stress-tolerance rapeseed have been extensively studied for many stresses, as shown in Table 3.

Transcriptomic Approaches: What Appears to Be Happening at TheTranscript Level?
Transcriptomic is a very promising technique to understand abiotic stress regulation in plants to decipher novel genes and various regulatory networks through transcriptome profiling. 131 Transcriptomic or/and gene expression investigation by next-generation sequencing (NGS), RNAseq profiling, subtractive libraries, expressed sequence tags (ESTs), serial analysis of gene expression (SAGE), and microarray have great potential to improve genomic resources of plants such as gene discovery and functional analysis. 132,133 Recently, numerous rapeseed genome sequencing and re-sequencing projects have been completed (Supplementary Table 1). Based on the NGS technologies, a Brassica napus pan-genome information resource (BnPIR) database http://cbi.hzau. edu.cn/bnapus/index.php) has been developed to facilitate the B. napus researchers in the post-genomic era. Global transcriptome profiling provides an excellent opportunity for comprehensive knowledge about gene expression and could help identify numerous regulatory mechanisms. In the subsequent segments, we have explained the potential of widely used approaches for studying gene expression at the transcript level. Table 4 shows a summary of transcriptome-based experiments performed in stressful conditions.

Modern Transcriptomic Analysis by RNA-seq
RNA-seq is an emerging approach that exploits or/ and offers a different outlook to examine the transcriptome sequence by granting complete access to transcripts. Therefore, RNA-seq can be conducted as a substitute strategy for many diverse techniques for quantification of the transcript with the advantage of higher sensitivity and ability to differentiate among related gene paralogs, which are different by just a small number of nucleotides. 133,135 For instance, five TFs families have been characterized and described under various abiotic stresses in rapeseed. Totally 2167 TFs from 5 different families were documented in rapeseed; i.e., 518 BnAP2/ ERF, 252 BnbZIP, 721 BnMYB, 398 BnNAC, and 278 BnWRKY, including some unique transcripts as compared to actual results. Many vital representatives of these TFs and regulatory systems associated with various abiotic stress conditions have been discovered. The investigations in rapeseed against stress tolerance have extended our knowledge toward TFs. RNA-seq represents that more than 80% of TFs triggers abiotic stress, and 315 TFs (DEGs) have been observed, and these 315 DEGs were highly expressed. 133 Yong and colleagues performed RNA-seq for the comparative transcriptomic study of rapeseed under increased salt stress. Roots and leaves were collected after 1 hour, and 12 hours of salt stress and de novo transcriptome sequencing yielded a total of 14,719 DEGs. Additionally, Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Ontology (GO) enrichment analysis found that 438 transporter genes with 582 TFs were influenced by salinity in roots and leaves. DEGs under RNA-seq analysis identified 3,657 transcripts triggered by exposure to drought stress. 136 Recently, RNA-seq was executed to elucidate the transcriptional modulation process for the fast growth of rapeseed. Various transcriptomic assemblies were established under cold stress and normal temperature with a slow and rapid germination speed rate. Transcriptome analysis showed 9111 and 10,233 DEGs, which were down and up-regulated under cold stress. Moreover, many TFs such as ERF, NAC, DREB, B3, MYB, EFR, bZIP, and WRKY were also found to regulate the low-temperature tolerance in rapid germination cultivars. These results will help future breeding programs to develop abiotic stress tolerance rapeseed genotypes. 138 In another study, under cold stress, RNA-seq was used to explore the molecular mechanisms in different rapeseed ecotypes. They identified 25,460 and 28,512 DEGs in spring and winter oilseed ecotype, respectively. Identified DEGs mainly fitted to lipid, ABA, secondary metabolism, signal transduction pathways, and these signaling pathways may play dynamic roles in both ecotypes under cold stress. 140 See Table 4 for more examples.

Expressed Sequence Tags (Ests)
ESTs signify a foundation for discovering unique gene structures that provide an outline for further significant studies, like expression system, gene maps, and cDNA sequencing projects. ESTs have been considered the precise technique to unveil sequences-related knowledge under abiotic stress conditions. 142,143 The ocsESTdb database provides information about seed ESTs and full-length CDS sequences of oilcrops seeds. The relative investigations of the oilseed databank showed that ESTs are accessible at the database of OCRI-CAAS, Wuhan, C h i n a ( h t t p : / / w w w . o c r i -g e n o m i c s . o r g / ocsESTdb/). 144 Similarly, overtly available Brassica ESTs contigs equivalent to a variety of gene functions (http://brassica.nbi.ac.uk/array_info.html).
Nevertheless, 343 WRKY domains with 287 genes were documented in response to several abiotic stresses in rapeseed. Microarray and EST-based analysis showed that 74 WRKY genes had been expressed beneath stress conditions. After QTL mapping, 77 WRKY genes have been reported in 31 QTL loci associated with many stress resistance. Twenty-six BnaWRKY genes which are triggered by drought, salinity and low-temperature stress. 128 Recently, available data of ESTs were examined and found 25 creatine phosphokinase (CPK) genes. A DH line of rapeseed was used to clone the cDNA sequences of 23 genes. Phylogenetic analysis was performed, and green fluorescence protein was used as a reporter gene to detect five candidates in BnaCPKs. Additionally, the expression of 21 BnaCPKs was investigated for oxidative, low potassium, abscisic acid, heat, cold, drought, and salinity stress regulation via qRT-PCR. The results suggested that multiple signaling pathways govern CPKs in response to several stresses in rapeseed. 26 Rapeseed EST profiling was carried out to find the function of typical AP2/ERF TFs under biotic and several abiotic stress regulations. 145 Table 1 documents the other TFs in response to abiotic stresses in rapeseed.

Serial Analysis of Gene Expression (SAGE)
SAGE has been extensively used to investigate gene expression. SAGE method calculates a tag, which shows a product of gene transcriptome. SAGE is considered the most economical and highthroughput approach, including mRNA isolation, cloning, and sequencing. In the SAGE technique, `tag` is a short length nucleotide sequence with a pointed head-to-head specific restriction enzyme. Therefore, SAGE represents gene expression in digital form. There are many SAGE applications in plants, such as the interaction between host and pathogens, plants' responses in several abiotic stresses, transcriptome profiling, and metabolism of many hazardous compounds. 146,147 About functional genomics investigations of oilseed plants with the importance of seed production and metabolism mechanism of fatty acids, a database was established named Shanghai RAPESEED database (RAPESEED, http://rapeseed.plantsignal.cn/). The rapeseed has 8462 ESTs, including 2526 full-length cDNA; 8095 expressed genes, and 23,895 SAGE tags during seed growth. In RAPESEED database, all the relevant data is stored in the form of nucleotides and protein sequences. 148 This technique has been used in several crops but needs to be considered for rapeseed in future work.

Microarray
cDNA microarrays are used for observing gene expression and offer a proficient strategy to evaluate the potential functions of numerous genes. 149 Microarray cDNA investigations of gene expression in various plants beneath several abiotic factors have been widely documented. 150,151 Gene databank accessibility gave plant gene expression from microarray investigations like Gene Expression Omnibus (https://www.ncbi.nlm.nih. gov/geo/) and ArrayExpress-functional genomics data (http://www.ebi.ac.uk/arrayexpress). 152 Microarray analysis was demonstrated in rapeseed to decipher the function of CBF/DREB1-like TFs under cold stress. Microarray and northern blot analysis confirm that the accumulation of coldresponsive genes that have a function in photosynthesis. Additionally, some other genes, such as GLK1 and GLK2-like TFs, responsible for chloroplast development, trips-p/pi translocator, and βamylase, were also produced. Hence, increased exchange rate of malate/oxaloacetate, enhancement in glycolysis, more sucrose and starch production, improved Calvin cycle enzymes, and rectification of photosynthetic efficacy was also detected, indicating that BnCBF hyper-expression has moderately imitated freezing-induced tolerance. Resulting in the overexpression of DREB1/BNCBF has shown improved not only cold tolerance but also controlled chloroplast development in rapeseed. 153 Therefore, it is essential from an economic point of view to increase rapeseed varieties with freezing tolerance (3-5°C) using CBF genes by means of the addition of millions of acres of lands to rapeseedproduction areas worldwide. 154 A comprehensive analysis of genes triggered by drought and salinity was performed by microarray to investigate the genes that govern abiotic stress reaction in rapeseed. The results indicated that out of 536 clones, 189 and 141 clones were responsible for gene supersession under salt and drought stress, while 288 and 172 were identified for drought and salinity resistance genes, respectively. The functional examination revealed that these genes play a vital part in the growth, abiotic stress-tolerance, hormone response, signal transduction, regulatory factors, and various metabolic activities in rapeseed. 155

Proteomics Approaches: What Makes It Happen?
Protein components of any living organism at a specific time are termed as proteome of that organism. At the beginning of 2000, due to the accessibility of whole-genome sequencing and mass spectrometry (MS) approaches, the proteomics strategy has been established successfully. To elaborate on the relationship between plant proteome with surrounding environmental stimuli, relative expression at the proteomic level can be studied by subjecting the plants to normal and abiotic stress conditions. 156,157 During the last decade, yeast two-hybrid (Y2H), matrixassisted laser desorption ionization (MALDI) and electrospray ionization (ESI)-MS, and one/twodimensional gel electrophoresis (2-DE) have gained much attention as excellent tools for separation and as analytical approaches in proteomics analysis. In the sub-sections, we have explained the potential of these approaches.
During abiotic stresses, the protein profiling of drought and salt stress of rapeseed has been conducted to detect the cross-talk between the cells through multiple reaction monitoring. Proteins related to phosphorylation mechanisms, such as CTRI, CDPK21, and TPR, have been identified under salt stress conditions. Similarly, BSL and STN7 proteins were also recognized, which have a role in the phosphorylation process under drought stress. 20 Nevertheless, an iTRAQproteomic analysis was carried out for rapeseed roots under waterlogging stress, and 7736 proteins were identified. These proteins function differently in response to stress and provide insight knowledge for adaptive mechanisms. 158 An experiment was performed on rapeseed for quantitative proteomic profiling under salt stress self-compatibility. Selfcompatibility induced by salt stress identified some unique proteins, which elucidate the molecular mechanisms underlying the breeding of rapeseed cultivars. 159

MALDI-TOF-MS and ESI
Nowadays, proteomics and metabolomics analysis of endogenous plant components have become very popular, and to carry out these investigations, a powerful tool such as MS imaging has been applied widely. Matrix-assisted laser desorption ionization (MALDI) and electrospray ionization (ESI) are mass spectrometry methods that have been extensively implemented for protein analysis. 160,161 MALDI-TOF-MS and ESI are wellestablished approaches to analyze the cell lysate of protein contents, separated by m/c ratio. 162 Ionization in MALDI can also be coupled with time of flight (TOF) analyzer. 164 Recently, a study has been reported on rapeseed leaves, in which proteomic matrix, physiological and biochemical variations were evaluated under salt and lipoid acid stress. Comparative proteomic investigations were carried out for control-grown leaves as well as leaves from plants subjected to salinity combined with exogenous lipoic acid (LA) application. The proteins of various sizes were dispersed using 2-DGE and found that 28 proteins have been expressed under stress conditions. Furthermore, for the exact confirmation of these 28 proteins, MALDI-TOF/TOF MS has been used and recognized 21 proteins. 163 2-DGE was used for comparative proteomic analysis of thermossensitive genic male sterility genotypes of rapeseed during microspore and microsporocyte formation. MALDI-TOF MS has identified 28 protein, from which ten protein expressed during microsporocyte while the remaining 18 protein expressed in the microspore phase. 165

Two-dimensional Gel Electrophoresis (2-DE)
In modern proteomic studies, 2-DE is regarded as the driving force. Despite the dominance of MS, this strategy still holds prime importance for proteomic analysis. In various protein separation methods, 2-DE is most promising and accepted as a separation method and an analytical approach because of its powerful separation ability. 166 For example, 2-DE was used to decipher the molecular networks regulating the salt stress in rapeseed. A salinity susceptible cultivar of rapeseed was subjected to different salt treatments and found that Na + content and proline concentration were enhanced in leaf. Therefore, K/Na + percentage, plant height, and shoot dry weight were reduced. 2-DE detected 110 spots on gels, and 37 of them indicated significantly abundant variations. Proteins were analyzed by employing LC-MS that has a function in photosynthesis and energy production. The results unveiled the reduction in energy production enzymes due to salt stress, whereas the increased accumulation of phosphoribulokinase under salinity in rapeseed. 167 2-DE was run to examine the physiological and proteomic regulations of rapeseed under salinity. Seedlings were subjected to different salt stress concentrations that result in reduced photosynthesis activity and growth arrest, and 44 proteins were detected by the spots which contained many saltresistance proteins. The results showed that the highly expressed proteins, which regulated tolerance, damage repair, and protein metabolism, might mitigate damaging impacts of salinity on respiration, energy production, photosynthesis, and chlorophyll synthesis in the leaves of rapeseed. This will help improve the understanding of the various molecular mechanisms operating under salinity in rapeseed and aid in developing GE rapeseed with increased salinity tolerance. 168 Recently, 2-DE was used for the separation of root proteins, while MALDI-TOF-MS was employed for protein identification under salinity. Different protein spots were detected and their abundance was significantly influenced by salinity. Functional studies demonstrated the nine categories of DEPs, while 14 protein categories were detected in tolerant genotypes. The most important findings are the DEPs associated with energy metabolism, redox regulation, heat shock proteins, fructose synthesis, and glycolysis mechanism was enhanced only in the salt-tolerant genotype rapeseed. 169 There are few databases available for proteomic analysis by using 2-DE, including rapeseed, rice, banana, tobacco, and Arabidopsis having protein profiles present at SWISS-2D-PAGE (https://world-2dpage.expasy. org/swiss-2dpage/) and WORLD-2D-PAGE (https://world-2dpage.expasy.org/list/). 170

Yeast Two-hybrid (Y2H)
Y2H system is a handy technique for genetic mapping and to exploit the various mechanism basal in protein-protein interactions by activating the reporter genes. 171 Y2H assay was conducted to identify the various amino acids having significant potential in modulating drought stress resistance factors like DREBs in rapeseed. 172 Y2H and bimolecular fluorescence complementation (BiFC) were executed for identification and cloning of protein phosphatase type 2 C (PP2C) and basic leucine zipper (bZIP) from rapeseed. It showed the interaction between BnaPP2Cs and BnaCPKs and unveiled the novel interaction among BnaCPK. 26 Y2H system was used to study the interaction among various CBLs and CIPKs proteins under several rapeseed abiotic stresses. Results show that 23 CIPK and 7 CBL genes were detected from rapeseed database research and cloning of 17 CIPKs and 6 CBLs cDNA sequences. Green fluorescence protein (GFP) was used to determine the subcellular detection of 2 BnaCIPKs and 3 BnaCBLs genes in rapeseed. Y2H assay was performed for protein interactions among 17 BnaCIPKs and 6 BnaCIPKs. Besides, the expression level of selected 12 BnaCIPKs and 6 BnaCBLs genes were analyzed under ABA, heat, cold, drought, and salinity stress via qRT-PCR. The findings revealed that CIPK and CBL families established a complicated signaling framework under several rapeseed abiotic factors. 27 Another experiment was conducted to elucidate the function of MPK and MKK protein families in multiple stresses. The amino acid sequence was predicted for both MPK and MKK through sequencing and phylogenetic analysis. To unveil the cellular localization reporter gene, GFP was used. For protein-protein interactions among MPK and MKK families, the Y2H assay was run, and the results were further assessed through BiFC assay. Moreover, the expression of selected MPKs and MKKs under multiple stresses was evaluated by using RT-PCR. The result showed that 12 MPK and 7 MKK genes had been identified, which can be employed as a marker to generate stresstolerance rapeseed. 173 Genetic studies documented that ds-3 is responsible for dwarfism in rapeseed. The proteomic evaluation was performed for rapeseed to elucidate the role of genes, BnaC07.RGA, BnaA06.RGA, BnaC09.RGA and BnaA09.RGA. qRT-PCR and Y2H strategies were used for BnaC09.RGA and BnaA09.RGA gene expression and identified that both these genes have a considerable impact on the production of semidwarf rapeseed. 174

Metabolomics: Are Metabolites Associated with the Closest Link to Phenotype?
To understand plant biochemistry at the organism and cellular level, metabolomics arising as a new era strategy to examine the whole metabolome of any crop plant. Due to its wide applications since the 1990s, metabolomics has been magnificently applied to plants to detect novel metabolites, genes and their metabolic pathways. 175 Using metabolomics, GM crops can be evaluated in terms of their improved agronomic characters. Metabolomics consists of different signaling pathways, the interaction between proteins, the involvement of plant primary and secondary metabolites, and the epigenetic regulation process. Primary and secondary metabolites of plants are crucial to regulating biological and biochemical mechanisms. [175][176][177] Metabolome analysis of high expression of the phospholipase C2 gene was studied in GE rapeseed and revealed that it has resistance against low temperature at a metabolomic level. GE plants show a remarkable increase in maltose and considerable enhancement in some free fatty acids, glycerol 3-phosphate and glycerol, stachyose, raffinose, and some flavonoids. 179 For metabolome profiling gas chromatography-mass spectrometry (GC-MS) approach has been used for various rapeseed cultivars. Out of 162 compounds, metabolic profiling of 52 compounds has been successfully achieved. Different multivariate tools were applied, which showed remarkable variance among different rapeseed varieties. 176 With the emergence of omics approaches, various researches have concentrated on elucidating the expression and function of several genes, proteins, and metabolites in rapeseed. Because of its commercial importance, oilproducing rapeseed has been subjected to MS tools to quantify and characterize rapeseed metabolome. Therefore, profiling of rapeseed metabolome aids in moving more deepen in plant biology and physiology to exploit an abiotic factor regulation. 179 Recently, 140 identified 41 differentially accumulated metabolites in the spring and 47 in the winter rapeseed ecotypes under cold stress. Notably, 81 metabolites primarily went to primary metabolites, including amino acids, organic acids, and sugars. They are suggesting that carbohydrates and amino acid compounds play a vital role in improving cold tolerance.
Metabolomics is yet to be reported for several abiotic stresses in rapeseed.

Metabolic QTL for Abiotic Stress Tolerance
For phenotypical and morphological determination, various biomarkers have been developed. Thus, metabolic QTL (mQTL) and metabolic GWAS (mGWAS) approaches have been used to predict phenotype and establishment of metabotypes. 180 For gene expression, protein and metabolome profiling are coupled with QTL mapping, as shown in Fig. 4. Genomic and metabolic markers are frequently correlated in mQTL mapping. In mQTL, a major difficulty arises in the detection of desired genes and metabolites. Therefore, a precise, measurable mapping of metabotypes is permitted to detect candidate gene. 176,179 Metabolic levels of fatty acids, G3P, glycerol, and maltose significantly rose in GE plants in cold stresses by elevated concentrations of flavonoids, raffinose, and other sugars. 181 Nuclear magnetic resonance (NMR)-based seed metabolites identification was carried out between two species, rapeseed and turnip. It was concluded that unsaturated fatty acids, sucrose, and sinapine are the most perspicacious metabolites influencing by changing the environment. 182 The LC-TOFMS-based metabolomic and allopathic analysis was performed to understand the chemistry of rapeseed allelochemicals and their ability to hinder root and shoot growth. 183

Phenomics: What Has Occurred?
The relationship between genotypes and phenotypes is very crucial for breeding programs. Plant phenomics is considered the phenotype of a plant or genotypic expression in a specific environmental condition. 184 Additionally, a plant's phenotype included several parameters that can be assessed through direct examination or by applying numerous analytical techniques and can also be defined by the association between environment and plant genotype. 185 Phenotyping is still a massive task under abiotic stress conditions due to complex biosynthesis processes that govern several abiotic stress tolerance in plants. 185 The significance of phenotyping has become apparent in the postgenomic era because the approaches used for crop improvement such as GWAS, GS, MAS, QTL mapping heavily depend upon the high-throughput phenotyping (HTP) in crops. 186 Nonetheless, HTP technologies have been getting tremendous advancement. Data mining, interpretation, and storage strategies are automated, precise, accurate, and economical. Genetic dissection of various characteristics and detailed examination of plant structure and function permits studying the plant phenotypic expression. 188 Recently, advanced HTP tools have been designed with multifunctional software coordination, consisting of X-ray tomography, hyperspectral imaging, and visible light imaging. This HTP allows the imaging of thousands of plants automatically at the same time. Many phenotyping centers have been set up in many countries (Table 5) and, notably, some unique QTLs have been documented in several plants. 187 Recently, a few studies have been conducted using HTP in rapeseed. For instance, to speed-up the dissection of the dynamic genetic architecture of rapeseed growth and yield under different developmental stages. 189 The phenotyping and genome-wide association mapping for the improvement of root architectural traits. 190 Moreover, it has been summarized that the integration of holistic phenotyping tools can elucidate the functional gene polymorphism and explain the complex mechanisms responsible for abiotic stress tolerance in crop plants. Notably, in rapeseed, the utilization of different HTP tools under environmental stresses is still lacking.

Transgenic Approaches
In the past few decades, transgenic methods have been widely used for developing abiotic stress tolerance plants. Genetic engineering for the development of stress resistance plants relies on the manipulation of genes responsible for stress regulation, which might be a way forward for enhancing plant health under stressful conditions. Assessment of the transgenic plants under stressful environments and regulation of physiological, biochemical, and cellular effects of the manipulated genes at the whole plant extent is still considered a persisting challenge to overwhelmed in rapeseed. So far, several transgenic rapeseed lines have been reported with improved abiotic stress tolerance (Table 6). For instance, transgenic rapeseed lines overexpressing Arabidopsis CBF1/2/3 genes exhibited improved freezing tolerance due to the introduction of CBF-targeted orthologous rapeseed Bn115 gene. 200 Likewise, homologous overexpression of BnCBF5 and BnCBF17 enhanced freezing tolerance in transgenic lines. 153 Whereas transgenic lines showed improved performance with BnCBF17 as compared to BnCBF5, possibly due to higher expression of cor genes under cold stress. 153 The transgenic lines expressing the AtPLD-α-1 gene from Arabidopsis thaliana show it improves tolerance to drought and salinity stresses. It also reduced the H 2 O loss, improve biomass, and yield production under stress conditions. 192 The hyperactive expression of the Arabidopsis AtDWF4 gene elevated seed productivity and tolerance to heat, drought, dehydration stresses and enhances the seed yield in transgenic lines. 195 The cloning of tobacco serine acetyltransferase (SAT; a ratelimiting enzyme for cysteine biosynthesis)encoding gene (NtSAT4) generated high levels of glutathione and cysteine in transgenic rapeseed lines for improved heavy metals tolerance. 197 In another study, the Arabidopsis thaliana AtTrx-h2 gene improves the salinity tolerance by modulating antioxidant defense systems in transgenic lines. 198 Several other examples are presented in Table 6.

CRISPR/Cas System: The Promising Genome Editing Tool
Genome editing is an efficient tool for crop improvement either by the loss-of-function, the gain-of-function, or a multiplex genome editing methods. Thus, clustered regularly interspaced short palindromic repeats/-associated proteins (CRISPR/Cas9) have come out as a robust GE strategy and are considered a fast, modest, and multipurpose procedure for GE and development of a transgene-free end-product. 48,202 The step-wise presentation of CRISPR/Cas9 based GE for the evolution of different stress-tolerance varieties of rapeseed is described in Fig. 5. Nevertheless, CRISPR/Cas9 mediated GE's mutation efficiency was observed and examined the heritability and pattern of gene manipulations in rapeseed. Interestingly, no off-target mutation was produced in mutated lines, and this investigation has opened new horizons for biotechnological applications in rapeseed for the development of stress-tolerance cultivars. 48 The difficulty of the rapeseed genome and gene redundancy is the main limiting factor for simultaneous mutagenesis of several homologs in the first progeny. Furthermore, the widespread identification of mutant plants is time-consuming through conventional approaches. 203 Recently, an expression cassette for sgRNA targeted five homologous genes, such as BnSPL3-Cnn, BnSPL3-C4, BnSPL3-C3, BnSPL3-A4, and BnSPL3-A5 have been developed. High-throughput sequencing investigation disclosed a very high knock out the efficiency of about 96.8% to 100% by CRISPR/ Cas9. 203 CRISPR/Cas9 based GE has excellent power in breeding programs to develop improved varieties for agronomic traits in many crops. However, the early exploitation of this tool in enlightening agronomic traits of rapeseed, e.g., the FAD2 gene, which controls the enzyme that catalyzes oleic acid desaturation in rapeseed, 204 the BnLLA10 gene which controls the lobed-leaf shape and regulates salt tolerance in rapeseed. 205 Moreover, the knockout of two BnaMAX1 homologs advances plant architecture and upsurges yield, 206 precise editing of CLAVATA genes normalizes silique development, 207 pod shatter resistance by the  208 and JAGGED genes, 209 flowering time and plant architecture by knockout of BnaTFL1 gene. 210 In a recent study, the gain-offunction mutant (bnaa6.rga-D) showed boosted drought tolerance, and its stomata were oversensitive to ABA signaling, whereas bnarga (lossof-function mutant) owned compact drought tolerance and less sensitivity to ABA signaling. 211,212 Notably, in rapeseed, the CRISPR/Cas9 system's utilization for the development of abiotic stress-tolerant rapeseed is still lacking and yet to be documented under several stress conditions.

Persisting Bottlenecks in the Production of Climate-resilient Rapeseed
Although marvelous advancement has been achieved in the biotechnological era, many questions and bottlenecks presently restrict the implementation of omics approaches for abiotic stress tolerance studies in rapeseed. Therefore, few bottlenecks demand to be abundantly handled to decipher the potential of omics tools for rapeseed (Fig.  6). Based on the available literature, there are very few abiotic stress tolerance rapeseed genotypes developed via omics tools. However, after the rapeseed genome sequence, researchers pay attention to Step-by-step presentation of CRISPR/Cas9 mediated genome editing for the development of different abiotic stress resistance varieties of rapeseed. Each step (1)(2)(3)(4)(5)(6)(7)(8) shows some basic sub-steps within the box (left side). In contrast, the right side indicates the practically on-table illustrations of the steps involved in the CRISPR/Cas9 mediated genome editing in rapeseed.
identify candidate genes and regulators to improve abiotic stress tolerance in rapeseed. Still, few genes have been reported for abiotic stresses.
Moreover, polygenic inheritance in abiotic stress tolerance rapeseed is still acting as a major bottleneck in conventional breeding programs. The misplacement of genetic divergence during the domestication of rapeseed is still considered a significant bottleneck among the existing ones. There is still a noticeable gap between the field and laboratory. However, less genetic diversity directly leads to less functional diversity. The biggest question is to utilize wild diversity more quickly, which can be utilized to explore genomic parts of loci related to essential QTL for abiotic stress tolerance in rapeseed.
Even though it is viable to identify thousands of metabolites, however, the precise identification of leftovers as the utmost bottleneck in plant metabolomics investigations. Insufficient knowledge and inadequate attempts on omics tools, mainly metabolomics, proteomics, and annotation mistakes in databases, are a significant barrier for functional characterization, and still act as significant bottlenecks in genome analysis. Figure 6. Persisting bottlenecks in the utilization of omics approaches to develop climate-resilient rapeseed. The dismissal of these bottlenecks using different molecular tools will help us to exploit the new manifesto to develop abiotic stress tolerance rapeseed; and successively will assure global food security.
However, the integration of newly emerged molecular platforms for identifying complex QTLs has remained a key restriction due to restricted potential to phenotype the crops precisely. Together, precise phenotyping concealed by native habitat is still a big phenotyping-bottleneck in several diverse development stages, including translation of genotype to phenotype. Another significant bottleneck is multiple homoeologs of a single gene in the rapeseed genome; in this regard, more homoeologs need to be targeted using GE tools. Thus, the dismissal of these bottlenecks using molecular tools will help us to exploit the new manifesto to develop stress resistance rapeseed; and successively will assure global food security.

Concluding Remarks
Rapidly changing climate is the main reason for several environmental stresses in the current era. Among them, abiotic stresses immensely affect rapeseed growth and production globally. These stresses may cause irregularities and a decrease in crop yield parameters. They can execute physiological, morphological, and molecular variations that deleteriously disturb production, growth, and final rapeseed yield. Therefore, it is vital to explore the stress-responsive mechanisms to enhance rapeseed production and quality under harsh environmental conditions. To solve this persisting issue, omics tools have demonstrated the most outstanding biotechnological applications to develop abiotic stresstolerance crops.
Omics, GE tools, and molecular breeding strategies have been extensively used to elucidate the complex biological mechanism and pathways regulating abiotic stress-tolerance in rapeseed. The multi-dimensional omics studies have gathered numerous datasets at the transcriptome, proteome, and metabolome level to unveil various molecular, physiological, and metabolic pathways related to abiotic stress-tolerance in rapeseed, which open ups new horizons for future investigations. However, few bottlenecks demand to be abundantly handled to decipher the potential of omics tools for rapeseed and other crops (Fig. 6). However, after the rapeseed genome sequence, researchers pay attention to identify candidate genes and regulators to improve stress tolerance in rapeseed. Still, few genes have been reported for multiple abiotic stresses. More work needs to be carried out to fully explore the beneficial role of omics in abiotic stress tolerance.
Molecular markers are the most powerful technology in plant molecular biology to determine the genetic variations in rapeseed at the polyploidy level. Additionally, with the accessibility of the rapeseed genome sequence, we can detect candidate genes related to several abiotic stresses in modern breeding programs. High-throughput sequencing technologies and EST construction for rapeseed are very promising for identifying SNPs for various abiotic stress-related QTLs. The applications of SNPs in rapeseed are very diverse due to its complex genome. Continuous improvements in NGS and genotyping techniques permit genotyping by sequencing, and SNPs will offer valuable information for rapeseed scientists. Moreover, genomic selection tools, along with HTP stages for selecting huge populations, permit more insights.

Future Directions
Genome editing via the CRISPR/Cas system and engineering stress-associated genes should be considered one of the most promising research directions to boost stress tolerance. Likewise, the engineering of metabolic pathways can open novel gaps for climate-resilient development, ready to grow rapeseed plants. Speed breeding has developed as a time-saving tool to expand plant growth and development under preferred conditions with enhanced stress tolerance. In the future, speed breeding will boost the genetic understanding and allow abiotic stress-tolerance rapeseed as established in other crops. Nevertheless, the CRISPR/ Cas9 system can be integrated with speed breeding to modernize world rapeseed production. Shortly, the combination of omics, genome editing, and speed breeding can speed up the rapeseed production with improved traits and increased abiotic stress tolerance. On the other hand, another emerging approach, "synthetic biology" can be mainly applied to plant biology and engineering methods to develop climate-smart rapeseed plants.

Acknowledgments
We are thankful to the researchers whose contributions have been cited in this review, which have helped us prepare this review paper. Further, the author also apologizes to all researchers whose relevant work could not be cited due to space limitations.

Disclosure statement
The authors declare no conflict of interest.

Funding
This work was supported by the Agricultural Science and Technology Innovation Program (ASTIP) and The Hubei Agricultural Science and Technology Innovation Center (2016-620-000-001-048).

Author Contributions
Ali Raza (AR) conceived the idea and wrote the manuscript. Ali Razzaq (ARa) and SSM wrote some parts in the initial draft. SSM, MAH, SW, HH, and QZ helped in the literature. AR prepared the tables and figures. AR, ZX, CY, and MH proofread and edited the manuscript. ZX and CY supervised the work. All authors have read and approved the final version of the manuscript.