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首页> 外文期刊>Chinese science bulletin >Genetic and physical mapping of AvrPi7, a novel avirulence gene of Magnaporthe oryzae using physical position-ready markers
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Genetic and physical mapping of AvrPi7, a novel avirulence gene of Magnaporthe oryzae using physical position-ready markers

机译:利用物理位置就绪标记对稻瘟病菌的新无毒基因AvrPi7进行遗传和物理定位

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摘要

Rice blast, caused by the fungal pathogen Magnaporthe oryzae, is one of the most devastating crop diseases worldwide. The avirulence gene corresponding to rice blast resistance gene Pi7 in field isolate CHL346 was inherited as a single gene, designated AvrPi7, in a segregating population consisting of 189 ascospore progenies derived from a cross between field isolates CHL346 and CHL42. In order to determine the chromosomal location of the AvrPi7 locus, a total of 121 simple sequence repeat (SSR) markers were developed based on the whole-genome sequence of reference isolate 70-15 of M. oryzae. Linkage analysis of the locus with these SSR markers showed that eight SSR markers on chromosome 1 were linked to the locus, among which the closest flanking markers MS1-9 and MS1-15 were 3.2 and 16.4 cM from the locus, respectively. For fine mapping, additional PCR-based makers including eight SSR markers and three candidate avirulence gene (CAG) markers were developed in the region flanking both markers. The AvrPi7 locus was genetically delimited within a 1.6-cM region flanked by markers MS1-21 and MS1-22, and co-segregated with the marker CAG2. To construct a physical map of the AvrPi7 locus, molecular markers linked to the Avr gene were mapped on the supercontigs of the reference isolate 70-15 through bioinformation analysis (BIA). Consequently, the AvrPi7 locus was delimited to a 75-kb interval flanked by markers MS1-21 and MS1-22 based on the reference sequence. Merodiploids observed in this study are also discussed.
机译:由真菌病原体稻瘟病菌引起的稻瘟病是世界上最具破坏性的农作物疾病之一。与分离株CHL346中的稻瘟病抗性基因Pi7相对应的无毒基因在由来自分离株CHL346和CHL42之间的杂交的189个子囊孢子代组成的分离群体中作为称为AvrPi7的单个基因遗传。为了确定AvrPi7基因座的染色体位置,基于米曲霉参照分离株70-15的全基因组序列,开发了总共121个简单序列重复(SSR)标记。用这些SSR标记对基因座进行的连锁分析表明,染色体1上有8个SSR标记与该基因座相连,其中最接近的侧翼标记MS1-9和MS1-15分别距该基因座3.2和16.4cM。为了进行精细定位,在两个标记两侧的区域中开发了其他基于PCR的标记,包括八个SSR标记和三个候选无毒力基因(CAG)标记。 AvrPi7基因座在1.6-cM区域内被遗传定界,两侧是标记MS1-21和MS1-22,并与标记CAG2共分离。为了构建AvrPi7基因座的物理图谱,通过生物信息分析(BIA)将链接到Avr基因的分子标记物定位在参考分离株70-15的超重叠群上。因此,基于参考序列,AvrPi7基因座被限定为一个75-kb的间隔,两侧是标记MS1-21和MS1-22。还讨论了在这项研究中观察到的二倍体。

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