4.7 Article

Genome- and transcriptome-wide association studies reveal the genetic basis and the breeding history of seed glucosinolate content in Brassica napus

期刊

PLANT BIOTECHNOLOGY JOURNAL
卷 20, 期 1, 页码 211-225

出版社

WILEY
DOI: 10.1111/pbi.13707

关键词

Brassica napus; glucosinolate; GTR2; GWAS; TWAS; co-expression; CRISPR; Cas9

资金

  1. National Key Research and Development Program of China [2016YFD0101000]
  2. National Natural Science Foundation of China [31571704]
  3. Natural Science Foundation of Hubei [2019CFA090]
  4. Wuhan Applied Foundational Frontier Project [2019020701011446]
  5. 111 Project [B20051]

向作者/读者索取更多资源

This study revealed the genetic structure and breeding history of low seed glucosinolates (SGC) improvement in rapeseed by GWAS and TWAS, identified 15 reliable QTLs associated with reduced SGC in modern cultivars, and highlighted the candidate gene BnaC02.GTR2. Experimental validation showed that BnaC02.GTR2 and its paralogs positively regulate seed glucosinolate accumulation, with implications for seed development and potential for crop improvement.
A high content of seed glucosinolates and their degradation products imposes anti-nutritional effects on livestock; therefore, persistent efforts are made to reduce the seed GSL content to increase the commercial value of rapeseed meal. Here, we dissected the genetic structure of SGC by genome-wide association studies (GWAS) combined with transcriptome-wide association studies (TWAS). Fifteen reliable quantitative trait loci (QTLs) were identified to be associated with the reduced SGC in modern B. napus cultivars by GWAS. Analysis of the selection strength and haplotypes at these QTLs revealed that low SGC was predominantly generated by the co-selection of qGSL.A02.2, qGSL.C02.1, qGSL.A09.2, and qGSL.C09.1. Integration of the results from TWAS, comprehensive bioinformatics, and POCKET algorithm analyses indicated that BnaC02.GTR2 (BnaC02g42260D) is a candidate gene underlying qGSL.C02.1. Using CRISPR/Cas9-derived Bna.gtr2s knockout mutants, we experimentally verified that both BnaC02.GTR2 and its three paralogs positively regulate seed GSL accumulation but negatively regulated vegetative tissue GSL contents. In addition, we observed smaller seeds with higher seed oil content in these Bna.gtr2 mutants. Furthermore, both RNA-seq and correlation analyses suggested that Bna.GTR2s might play a comprehensive role in seed development, such as amino acid accumulation, GSL synthesis, sugar assimilation, and oil accumulation. This study unravels the breeding selection history of low-SGC improvement and provides new insights into the molecular function of Bna.GTR2s in both seed GSL accumulation and seed development in B. napus.

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