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利用简单序列重复标记鉴定高粱PI 550610中对绿蝽生物型E抗性的一个主要数量性状位点

Identification of a major quantitative trait locus conditioning resistance to greenbug biotype E in sorghum PI 550610 using simple sequence repeat markers.

作者信息

Wu Y Q, Huang Yinghua, Porter David R, Tauer C G, Hollaway Lindsey

机构信息

USDA-ARS Plant Science Research Laboratory, 1301 N. Western Rd., Stillwater, OK 74075, USA,

出版信息

J Econ Entomol. 2007 Oct;100(5):1672-8. doi: 10.1603/0022-0493(2007)100[1672:ioamqt]2.0.co;2.

DOI:10.1603/0022-0493(2007)100[1672:ioamqt]2.0.co;2
PMID:17972647
Abstract

Greenbug, Schizaphis graminum (Rondani), represents the most important pest insect of sorghum, Sorghum bicolor (L.) Moench, in the Great Plains of the United States. Biotype E is the most widespread and dominant type not only in sorghum and wheat, Triticum aestivum L., fields, but also on many noncultivated grass species. This study was designed to determine sorghum accession PI 550610 resistance to greenbug biotype E, to map the resistance quantitative trait loci (QTLs) by using an established simple sequence repeat (SSR) linkage map and to identify SSR markers closely linked to the major resistance QTLs. In greenhouse screening tests, seedlings of PI 550610 showed strong resistance to the greenbug at a level similar to resistant accession PI550607. For QTL mapping, one F2 population containing 277 progeny and one population containing 233 F2:3 families derived from Westland A line x PI 550610 were used to genotype 132 polymorphic SSR markers and to phenotype seedling resistance to greenbug feeding. Phenotypic evaluation of sorghum seedling damage at 7, 12, 17, and 21 d postinfestation in the F2:3 families revealed that resistance variation was normally distributed. Single marker analysis indicated 16 SSRs spread over five chromosomes were significant for greenbug resistance. Composite interval and multiple interval mapping procedures indicated that a major QTL resided in the interval of 6.8 cM between SSR markers Xtxp358 and Xtxp289 on SBI-09. The results will be valuable in the development of new greenbug biotype E resistant sorghum cultivars and for the further characterization of major genes by map-based cloning.

摘要

麦二叉蚜(Schizaphis graminum (Rondani))是美国大平原地区高粱(Sorghum bicolor (L.) Moench)最重要的害虫。E生物型不仅在高粱和小麦(Triticum aestivum L.)田中分布最广且占主导地位,在许多非栽培草种上也是如此。本研究旨在确定高粱种质PI 550610对麦二叉蚜E生物型的抗性,利用已建立的简单序列重复(SSR)连锁图谱对抗性数量性状位点(QTL)进行定位,并鉴定与主要抗性QTL紧密连锁的SSR标记。在温室筛选试验中,PI 550610的幼苗对麦二叉蚜表现出强抗性,抗性水平与抗性种质PI550607相似。为了进行QTL定位,使用了一个包含277个后代的F2群体和一个由Westland A系与PI 550610杂交得到的包含233个F2:3家系的群体,对132个多态性SSR标记进行基因分型,并对幼苗对麦二叉蚜取食的抗性进行表型分析。对F2:3家系在接虫后7、12、17和21天的高粱幼苗损伤进行表型评估,结果表明抗性变异呈正态分布。单标记分析表明,分布在五条染色体上的16个SSR标记对麦二叉蚜抗性具有显著影响。复合区间和多区间作图程序表明,一个主要QTL位于SBI-09染色体上SSR标记Xtxp358和Xtxp289之间6.8 cM的区间内。这些结果对于开发新的抗麦二叉蚜E生物型高粱品种以及通过图位克隆进一步鉴定主要基因具有重要价值。

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