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与抗小麦条锈病的 YR5 基因共分离的抗性基因类似物多态性标记。

Resistance gene-analog polymorphism markers co-segregating with the YR5 gene for resistance to wheat stripe rust.

作者信息

Yan G P, Chen X M, Line R F, Wellings C R

机构信息

Department of Plant Pathology, Washington State University, USA.

出版信息

Theor Appl Genet. 2003 Feb;106(4):636-43. doi: 10.1007/s00122-002-1109-8. Epub 2002 Nov 2.

Abstract

The Yr5 gene confers resistance to all races of the stripe rust pathogen ( Puccinia striiformis f. sp. tritici) of wheat in the United States. To develop molecular markers for Yr5, a BC(7):F(3) population was developed by backcrossing the Yr5 donor ' Triticum spelta album' (TSA) with the recurrent parent 'Avocet Susceptible' (AVS). Seedlings of the Yr5 near-isogenic lines (AVS/6* Yr5), AVS, TSA, and the BC(7):F(3) lines were tested with North American races of P. striiformis f. sp. tritici under controlled greenhouse conditions. The single gene was confirmed by a 1:2:1 segregation ratio for homozygous-resistant, heterozygous and homozygous-susceptible BC(7):F(3) lines. Genomic DNA was extracted from the parents (the Yr5 near-isogenic line and AVS) and 202 BC(7):F(3) lines. The resistance gene-analog polymorphism (RGAP) technique was used to identify molecular markers. The parents and the homozygous-resistant and homozygous-susceptible BC(7):F(3) bulks were used to identify putative RGAP markers for Yr5. Association of the markers with Yr5 was determined using segregation analysis with DNA from the individual BC(7):F(3) lines. Of 16 RGAP markers confirmed by segregation analysis with 109 BC(7):F(3) lines, and nine of the markers confirmed with an additional 93 BC(7):F(3) lines, three markers co-segregated with the resistance allele and three markers co-segregated with the susceptibility allele at the Yr5 locus. The other four markers were tightly linked to the locus. Analysis of a set of Chinese Spring nulli-tetrasomic lines with three markers that co-segregated with, or were linked to, the susceptibility allele confirmed that the Yr5 locus is on chromosome 2B. Of five RGAP markers that were cloned and sequenced, markers Xwgp-17 and Xwgp-18 that co-segregated with the Yr5 locus were co-dominant and had 98% homology with each other in both DNA and translated amino-acid sequences. The two markers had 97% homology with a resistance gene-like sequence from Aegilops ventricosa and had significant homology with many known plant resistance genes, resistance gene analogs and expressed sequence tags (ESTs) from wheat and other plant species. The markers Xwgp-17 and Xwgp-18 also had significant homology with the NB-ARC domain that is in several genes for plant resistance to diseases, nematode cell death and human apoptotic signaling. These markers should be useful to clone Yr5 and combine Yr5 with other genes for durable and superior resistance for the control of stripe rust.

摘要

Yr5基因赋予美国小麦对条锈病病原菌(条形柄锈菌小麦专化型)的所有生理小种的抗性。为了开发Yr5的分子标记,通过将Yr5供体“斯卑尔脱小麦”(TSA)与轮回亲本“感病阿沃塞特”(AVS)回交,构建了一个BC(7):F(3)群体。在可控温室条件下,用北美条形柄锈菌小麦专化型的生理小种对Yr5近等基因系(AVS/6*Yr5)、AVS、TSA以及BC(7):F(3)株系的幼苗进行了测试。纯合抗性、杂合和纯合感病的BC(7):F(3)株系呈现1:2:1的分离比,证实该抗性由单基因控制。从亲本(Yr5近等基因系和AVS)以及202个BC(7):F(3)株系中提取了基因组DNA。采用抗性基因类似物多态性(RGAP)技术来鉴定分子标记。利用亲本以及纯合抗性和纯合感病的BC(7):F(3)混合群体来鉴定Yr5的假定RGAP标记。通过对单个BC(7):F(3)株系的DNA进行分离分析,确定标记与Yr5的关联性。在对109个BC(7):F(3)株系进行分离分析后,有16个RGAP标记得到确认,另外93个BC(7):F(3)株系进一步确认了其中9个标记,在Yr5位点上,有3个标记与抗性等位基因共分离,3个标记与感病等位基因共分离。其他4个标记与该位点紧密连锁。用3个与感病等位基因共分离或连锁的标记对一套中国春缺体-四体系进行分析,证实Yr5位点位于2B染色体上。在克隆并测序的5个RGAP标记中,与Yr5位点共分离的标记Xwgp-17和Xwgp-18是共显性的,其DNA序列和翻译后的氨基酸序列彼此具有98%的同源性。这两个标记与来自节节麦的一个类抗性基因序列具有97%的同源性,并且与许多已知的植物抗性基因、抗性基因类似物以及来自小麦和其他植物物种的表达序列标签(EST)具有显著同源性。标记Xwgp-17和Xwgp-18还与植物抗病、线虫细胞死亡和人类凋亡信号传导的几个基因中的NB-ARC结构域具有显著同源性。这些标记对于克隆Yr5以及将Yr5与其他基因组合以实现对条锈病持久且优异的抗性控制应该是有用的。

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