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Leptosphaeria maculans 无毒基因对应油菜 LepR1 抗性基因的遗传图谱定位。

Genetic mapping of the Leptosphaeria maculans avirulence gene corresponding to the LepR1 resistance gene of Brassica napus.

机构信息

Department of Plant Science, University of Manitoba, Winnipeg, MB, R3T 2N2, Canada.

出版信息

Theor Appl Genet. 2012 Feb;124(3):505-13. doi: 10.1007/s00122-011-1724-3. Epub 2011 Oct 30.

Abstract

AvrLepR1 of the fungal pathogen Leptosphaeria maculans is the avirulence gene that corresponds to Brassica LepR1, a plant gene controlling dominant, race-specific resistance to this pathogen. An in vitro cross between the virulent L. maculans isolate, 87-41, and the avirulent isolate, 99-56, was performed in order to map the AvrLepR1 gene. The disease reactions of the 94 of the resulting F(1) progenies were tested on the canola line ddm-12-6s-1, which carries LepR1. There were 44 avirulent progenies and 50 virulent progenies suggesting a 1:1 segregation ratio and that the avirulence of 99-56 on ddm-12-6s-1 is controlled by a single gene. Tetrad analysis also indicated a 1:1 segregation ratio. The AvrLepR1 gene was positioned on a genetic map of L. maculans relative to 259 sequence-related amplified polymorphism (SRAP) markers, two cloned avirulence genes (AvrLm1 and AvrLm4-7) and the mating type locus (MAT1). The genetic map consisted of 36 linkage groups, ranging in size from 13.1 to 163.7 cM, and spanned a total of 2,076.4 cM. The AvrLepR1 locus was mapped to linkage group 4, in the 13.1 cM interval flanked by the SRAP markers SBG49-110 and FT161-223. The AvrLm4-7 locus was also positioned on linkage group 4, close to but distinct from the AvrLepR1 locus, in the 5.4 cM interval flanked by FT161-223 and P1314-300. This work will make possible the further characterization and map-based cloning of AvrLepR1. A combination of genetic mapping and pathogenicity tests demonstrated that AvrLepR1 is different from each of the L. maculans avirulence genes that have been characterized previously.

摘要

真菌病原菌 Lepetosphaeria maculans 的 AvrLepR1 是无毒基因,与植物基因 Brassica LepR1 相对应,后者控制该病原菌的显性、种特异性抗性。为了定位 AvrLepR1 基因,在具有毒性的 L. maculans 分离株 87-41 和无毒的分离株 99-56 之间进行了体外杂交。对产生的 94 个 F1 后代的疾病反应在携带 LepR1 的油菜品系 ddm-12-6s-1 上进行了测试。有 44 个无毒后代和 50 个有毒后代,表明分离比为 1:1,并且 99-56 在 ddm-12-6s-1 上的无毒是由单个基因控制的。四分体分析也表明了 1:1 的分离比。AvrLepR1 基因相对于 L. maculans 的 259 个序列相关扩增多态性 (SRAP) 标记、两个克隆的无毒基因 (AvrLm1 和 AvrLm4-7) 和交配型基因座 (MAT1) 在遗传图谱上进行了定位。遗传图谱由 36 个连锁群组成,大小从 13.1 到 163.7cM,总跨度为 2076.4cM。AvrLepR1 基因座定位于连锁群 4,位于 SRAP 标记 SBG49-110 和 FT161-223 之间的 13.1cM 区间内。AvrLm4-7 基因座也定位于连锁群 4,靠近但不同于 AvrLepR1 基因座,位于 FT161-223 和 P1314-300 之间的 5.4cM 区间内。这项工作将使进一步表征和基于图谱的克隆 AvrLepR1 成为可能。遗传图谱和致病性测试的组合表明,AvrLepR1 与以前已鉴定的每个 Lepetosphaeria maculans 无毒基因不同。

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