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首页> 外文期刊>Theoretical and Applied Genetics >Genetic mapping of the Leptosphaeria maculans avirulence gene corresponding to the LepR1 resistance gene of Brassica napus
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Genetic mapping of the Leptosphaeria maculans avirulence gene corresponding to the LepR1 resistance gene of Brassica napus

机译:甘蓝型油菜LepR1抗性基因对应的黄腐杆菌的无毒力基因的遗传定位。

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摘要

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 F1 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.
机译:真菌病原体黄斑狼疮的AvrLepR1是无毒力基因,对应于芸苔属LepR1,这是一种控制该病原体的显性种族特异性抗性的植物基因。为了对AvrLepR1基因作图,在强毒的黄斑狼疮分离株87-41和无毒分离株99-56之间进行了体外杂交。在带有LepR1的双低油菜系ddm-12-6s-1上测试了94个F1 后代的疾病反应。有44个无毒后代和50个有毒后代,表明1:1的分离比率,并且ddm-12-6s-1上99-56的无毒力是由单个基因控制的。 Tetrad分析还显示了1:1的分离比率。相对于259个与序列相关的扩增多态性(SRAP)标记,两个克隆的无毒力基因(AvrLm1和AvrLm4-7)和交配型基因座(MAT1),AvrLepR1基因定位在黄斑狼疮的遗传图谱上。遗传图谱由36个连锁组组成,大小从13.1到163.7 cM不等,共跨越2,076.4 cM。 AvrLepR1基因座以SRAP标记SBG49-110和FT161-223侧翼的13.1 cM间隔定位到连锁群4。在FT161-223和P1314-300两侧的5.4 cM间隔中,AvrLm4-7基因座也位于连锁群4上,靠近但与AvrLepR1基因座不同。这项工作将使AvrLepR1的进一步表征和基于图的克隆成为可能。遗传图谱和致病性测试的组合表明,AvrLepR1与以前鉴定过的每个斑节对虾无毒力基因不同。

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  • 来源
    《Theoretical and Applied Genetics》 |2012年第3期|505-513|共9页
  • 作者单位

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

    Agriculture and Agri-Food Canada Saskatoon Research Centre Saskatoon SK S7N 0X2 Canada;

    Agriculture and Agri-Food Canada Saskatoon Research Centre Saskatoon SK S7N 0X2 Canada;

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

    Crop Development Centre College of Agriculture and Bioresources University of Saskatchewan 3C02 Agriculture Building 51 Campus Drive Saskatoon SK S7N 5A8 Canada;

    Agriculture and Agri-Food Canada Saskatoon Research Centre Saskatoon SK S7N 0X2 Canada;

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

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

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