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利用重测序进行粳稻品种抗穗发芽的 QTL 定位。

QTL mapping for pre-harvest sprouting resistance in japonica rice varieties utilizing genome re-sequencing.

机构信息

Department of Agricultural Biotechnology, National Institute of Agricultural Sciences, Rural Development Administration (RDA), Jeonju, 54874, South Korea.

Cheorwon Branch, National Institute of Crop Science, Rural Development Administration (RDA), Cheorwon, 24010, South Korea.

出版信息

Mol Genet Genomics. 2020 Sep;295(5):1129-1140. doi: 10.1007/s00438-020-01688-4. Epub 2020 May 26.

Abstract

Pre-harvest sprouting (PHS) leads to serious economic losses because of reductions in yield and quality. To analyze the quantitative trait loci (QTLs) for PHS resistance in japonica rice, PHS rates on panicles were measured in 160 recombinant inbred lines (RILs) derived from a cross between the temperate japonica varieties Odae (PHS resistant) and Unbong40 (PHS susceptible) under two different environmental conditions-field (summer) and greenhouse (winter) environments. Genome re-sequencing of the parental varieties detected 266,773 DNA polymorphisms including 248,255 single nucleotide polymorphisms and 18,518 insertions/deletions. We constructed a genetic map comprising 239 kompetitive allele-specific PCR and 49 cleaved amplified polymorphic sequence markers. In the field environment, two major QTLs, qPHS-3 and qPHS-11, were identified on chromosomes 3 and 11, respectively, whereas three major QTLs, qPHS-3, qPHS-4, and qPHS-11, were identified on chromosomes 3, 4, and 11, respectively, in the greenhouse environment. qPHS-11 and qPHS-11 had similar locations on chromosome 11, suggesting the existence of a gene conferring stable PHS resistance effects under different environmental conditions. The QTLs identified in this study can be used to improve the PHS resistance of japonica varieties, and they may improve our understanding of the genetic basis of PHS resistance.

摘要

采前发芽(PHS)会导致产量和质量下降,从而造成严重的经济损失。为了分析粳稻 PHS 抗性的数量性状位点(QTL),在两个不同的环境条件下——田间(夏季)和温室(冬季)——测量了由温带粳稻品种 Odae(PHS 抗性)和 Unbong40(PHS 敏感)杂交产生的 160 个重组自交系(RIL)的穗部 PHS 率。对亲本品种进行基因组重测序检测到 266773 个 DNA 多态性,包括 248255 个单核苷酸多态性和 18518 个插入/缺失。我们构建了一个遗传图谱,包括 239 个竞争性等位基因特异性 PCR 和 49 个切割扩增多态性序列标记。在田间环境下,在第 3 号和第 11 号染色体上分别鉴定到两个主要的 QTL,qPHS-3 和 qPHS-11,而在温室环境下,在第 3 号、第 4 号和第 11 号染色体上分别鉴定到三个主要的 QTL,qPHS-3、qPHS-4 和 qPHS-11。qPHS-11 和 qPHS-11 在第 11 号染色体上的位置相似,表明存在一个赋予不同环境条件下稳定 PHS 抗性效应的基因。本研究中鉴定的 QTL 可用于提高粳稻品种的 PHS 抗性,并且可能提高我们对 PHS 抗性遗传基础的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0508/7391406/ac5200e98c00/438_2020_1688_Fig1_HTML.jpg

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