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多年生黑麦草(Lolium perenne L.)病原体防御反应候选基因中单核甘酸多态性的发现与基因定位

Discovery and genetic mapping of single nucleotide polymorphisms in candidate genes for pathogen defence response in perennial ryegrass (Lolium perenne L.).

作者信息

Dracatos P M, Cogan N O I, Dobrowolski M P, Sawbridge T I, Spangenberg G C, Smith K F, Forster J W

机构信息

Department of Primary Industries, Biosciences Research Division, La Trobe Research and Development Park, Bundoora, VIC 3083, Australia.

出版信息

Theor Appl Genet. 2008 Jul;117(2):203-19. doi: 10.1007/s00122-008-0766-7. Epub 2008 May 1.

Abstract

Susceptibility to foliar pathogens commonly causes significant reductions in productivity of the important temperate forage perennial ryegrass. Breeding for durable disease resistance involves not only the deployment of major genes but also the additive effects of minor genes. An approach based on in vitro single nucleotide polymorphism (SNP) discovery in candidate defence response (DR) genes has been used to develop potential diagnostic genetic markers. SNPs were predicted, validated and mapped for representatives of the pathogenesis-related (PR) protein-encoding and reactive oxygen species (ROS)-generating gene classes. The F(1)(NA(6) x AU(6)) two-way pseudo-test cross population was used for SNP genetic mapping and detection of quantitative trait loci (QTLs) in response to a crown rust field infection. Novel resistance QTLs were coincident with mapped DR gene SNPs. QTLs on LG3 and LG7 also coincided with both herbage quality QTLs and candidate genes for lignin biosynthesis. Multiple DR gene SNP loci additionally co-located with QTLs for grey leaf spot, bacterial wilt and crown rust resistance from other published studies. Further functional validation of DR gene SNP loci using methods such as fine-mapping and association genetics will improve the efficiency of parental selection based on superior allele content.

摘要

对叶部病原体的易感性通常会导致重要的温带饲用多年生黑麦草的生产力显著下降。培育持久抗病性不仅涉及主要基因的部署,还涉及次要基因的累加效应。一种基于在候选防御反应(DR)基因中进行体外单核苷酸多态性(SNP)发现的方法已被用于开发潜在的诊断性遗传标记。对病程相关(PR)蛋白编码和活性氧(ROS)生成基因类别的代表进行了SNP预测、验证和定位。F(1)(NA(6)×AU(6))双伪测交群体用于SNP遗传图谱构建和响应冠锈病田间感染的数量性状位点(QTL)检测。新的抗性QTL与定位的DR基因SNP一致。LG3和LG7上的QTL也与牧草品质QTL和木质素生物合成的候选基因一致。来自其他已发表研究的多个DR基因SNP位点还与灰斑病、青枯病和冠锈病抗性的QTL共定位。使用精细定位和关联遗传学等方法对DR基因SNP位点进行进一步的功能验证,将提高基于优良等位基因含量的亲本选择效率。

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