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Genome-wide variations analysis of sorghum cultivar Hongyingzi for brewing Moutai liquor.


ABSTRACT: BACKGROUND:Hongyingzi is a sorghum (Sorghum bicolor L. Moench) cultivar for brewing Moutai liquor. For an overall understanding of the whole genome of Hongyingzi, we performed whole-genome resequencing technology to reveal its comprehensive variations. RESULTS:Compared with the BTx623 reference genome, we uncovered 1,885,774 single nucleotide polymorphisms (SNPs), 309,381 small fragments insertions and deletions (Indels), 31,966 structural variations (SVs), and 217,273 copy number variations (CNVs). These alterations conferred 29,614 gene variations. It was also predicted that 35 gene variations were related to the multidrug and toxic efflux (MATE) transporter, chalcone synthase (CHS), ATPase isoform 10 (AHA10) transporter, dihydroflavonol-4-reductase (DFR), the laccase 15 (LAC15), flavonol 3'-hydroxylase (F3'H), flavanone 3-hydroxylase (F3H), O-methyltransferase (OMT), flavonoid 3'5' hydroxylase (F3'5'H), UDP-glucose:sterol-glucosyltransferase (SGT), flavonol synthase (FLS), and chalcone isomerase (CHI) involved in the tannin synthesis. CONCLUSIONS:These results would provide theoretical supports for the molecular markers developments and gene function studies related to the tannin synthesis, and the genetic improvement of liquor-making sorghum based on the genome editing technology.

SUBMITTER: Zhou L 

PROVIDER: S-EPMC7227080 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Genome-wide variations analysis of sorghum cultivar Hongyingzi for brewing Moutai liquor.

Zhou Lingbo L   Wang Can C   Gao Xu X   Ding Yanqing Y   Cheng Bin B   Zhang Guobing G   Cao Ning N   Xu Yan Y   Shao Mingbo M   Zhang Liyi L  

Hereditas 20200514 1


<h4>Background</h4>Hongyingzi is a sorghum (Sorghum bicolor L. Moench) cultivar for brewing Moutai liquor. For an overall understanding of the whole genome of Hongyingzi, we performed whole-genome resequencing technology to reveal its comprehensive variations.<h4>Results</h4>Compared with the BTx623 reference genome, we uncovered 1,885,774 single nucleotide polymorphisms (SNPs), 309,381 small fragments insertions and deletions (Indels), 31,966 structural variations (SVs), and 217,273 copy number  ...[more]

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