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Integration of GWAS and transcriptome analyses to identify SNPs and candidate genes for aluminum tolerance in rapeseed (Brassica napus L.)

文献类型： 外文期刊

作者： Zhou, Huiwen 1 ; Xiao, Xiaojun 1 ; Asjad, Ali 4 ; Han, Depeng 1 ; Zheng, Wei 3 ; Xiao, Guobin 3 ; Huang, Yingjin 1 ; Zhou, Qinghong 1 ;

作者机构： 1.Jiangxi Agr Univ, Key Lab Crop Physiol Ecol & Genet Breeding, Minist Educ Jiangxi Prov, Nanchang 330045, Jiangxi, Peoples R China

2.Jiujiang Univ, Inst Jiangxi Oil Tea Camellia, Jiujiang 332005, Jiangxi, Peoples R China

3.Jiangxi Inst Red Soil, Jinxian 331717, Jiangxi, Peoples R China

4.Dept Agr & Fisheries, POB 1054, Mareeba, Qld 4880, Australia

关键词： Brassica napus; Aluminum; Genome-wide association study; Transcriptomic analysis; Candidate gene

期刊名称：BMC PLANT BIOLOGY （ 影响因子：5.26； 五年影响因子：5.761 ）

ISSN： 1471-2229

年卷期： 2022 年 22 卷 1 期

页码：

收录情况： SCI

摘要： Background The exchangeable aluminum (Al), released from the acid soils, is another addition to the environmental stress factors in the form of Al toxicity stress. Al stress affects the normal crop development and reduces the overall yield of rapeseed (Brassica napus L.). The response mechanism of plants to Al toxicity is complicated and difficult to understand with few QTL related studies in rapeseed under Al toxicity stress. Result Using 200,510 SNPs developed by SLAF-seq (specific-locus amplified fragment sequencing) technology, we carried out the genome-wide association analysis (GWAS) in a population of 254 inbred lines of B. napus with large genetic variation and Al-tolerance differences. There were 43 SNPs significantly associated with eight Al-tolerance traits in the seedling stage were detected on 14 chromosomes, and 777 candidate genes were screened at the flanking 100 kb region of these SNPs. Moreover, RNA-seq detected 8291 and 5341 DEGs (the differentially expressed gene) in the Al -tolerant line (ATL) and -sensitive line (ASL), respectively. Based on integration of GWAS and RNA-seq analysis, 64 candidate genes from GWAS analysis differentially expressed at least once in 6 h vs 0 h or 24 h vs 0 h conditions in ATL or ASL. Moreover, four out of sixty-four candidate genes (BnaA03g30320D, BnaA10g11500D, BnaC03g38360D and BnaC06g30030D) were differentially expressed in both 6 h and 24 h compared to 0 h (control) conditions in both lines. The proposed model based on the candidate genes excavated in this study highlighted that Al stress disturb the oxidation-redox balance, causing abnormal synthesis and repair of cell wall and ABA signal transduction, ultimately resulting in inhibition of root elongation. Conclusions The integration of GWAS and transcriptome analysis provide an effective strategy to explore the SNPs and candidate genes, which has a potential to develop molecular markers for breeding Al tolerant rapeseed varieties along with theoretical basis of molecular mechanisms for Al toxicity response of Brassica napus plants.

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