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LrSV2的精细定位,LrSV2是小麦3BS染色体上一个具有小种特异性的成株期抗叶锈病基因。

Fine mapping of LrSV2, a race-specific adult plant leaf rust resistance gene on wheat chromosome 3BS.

作者信息

Diéguez M J, Pergolesi M F, Velasquez S M, Ingala L, López M, Darino M, Paux E, Feuillet C, Sacco F

机构信息

Instituto de Genética "Ewald A. Favret" CICVyA-INTA CC25 (1712) Castelar, Buenos Aires, Argentina,

出版信息

Theor Appl Genet. 2014 May;127(5):1133-41. doi: 10.1007/s00122-014-2285-z. Epub 2014 Feb 20.

Abstract

Fine mapping permits the precise positioning of genes within chromosomes, prerequisite for positional cloning that will allow its rational use and the study of the underlying molecular action mechanism. Three leaf rust resistance genes were identified in the durable leaf rust resistant Argentinean wheat variety Sinvalocho MA: the seedling resistance gene Lr3 on distal 6BL and two adult plant resistance genes, LrSV1 and LrSV2, on chromosomes 2DS and 3BS, respectively. To develop a high-resolution genetic map for LrSV2, 10 markers were genotyped on 343 F2 individuals from a cross between Sinvalocho MA and Gama6. The closest co-dominant markers on both sides of the gene (3 microsatellites and 2 STMs) were analyzed on 965 additional F2s from the same cross. Microsatellite marker cfb5010 cosegregated with LrSV2 whereas flanking markers were found at 1 cM distal and at 0.3 cM proximal to the gene. SSR markers designed from the sequences of cv Chinese Spring BAC clones spanning the LrSV2 genetic interval were tested on the recombinants, allowing the identification of microsatellite swm13 at 0.15 cM distal to LrSV2. This delimited an interval of 0.45 cM around the gene flanked by the SSR markers swm13 and gwm533 at the subtelomeric end of chromosome 3BS.

摘要

精细定位能够实现基因在染色体上的精确定位,这是定位克隆的前提条件,而定位克隆有助于合理利用基因并研究其潜在的分子作用机制。在持久抗叶锈病的阿根廷小麦品种Sinvalocho MA中鉴定出了三个抗叶锈病基因:位于6BL远端的幼苗抗性基因Lr3,以及分别位于2DS和3BS染色体上的两个成株抗性基因LrSV1和LrSV2。为了构建LrSV2的高分辨率遗传图谱,对Sinvalocho MA与Gama6杂交产生的343个F2个体进行了10个标记的基因分型。在同一杂交组合的另外965个F2个体上分析了该基因两侧最紧密的共显性标记(3个微卫星标记和2个STM标记)。微卫星标记cfb5010与LrSV2共分离,而在该基因的远端1 cM和近端0.3 cM处发现了侧翼标记。对跨越LrSV2遗传区间的中国春BAC克隆序列设计的SSR标记在重组体上进行了测试,从而在LrSV2远端0.15 cM处鉴定出微卫星标记swm13。这将该基因周围限定在一个0.45 cM的区间内,两侧分别是位于3BS染色体亚端粒末端的SSR标记swm13和gwm533。

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