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Cloning of a Resistance Gene Analog from Wheat and Development of a Codominant PCR Marker for Pm21 被引量:10
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作者 Ya-Ping Chen Hua-Zhong Wang Ai-Zhong Cao Chun-Mei Wang Pei-Du Chen 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2006年第6期715-721,共7页
To Investigate the mechanism of resistance to wheat (Triticum aestivum L.) powdery mildew, suppression subtractlve hybridization was conducted between an isogenic resistant line carrying Pm21 and its recurrent paren... To Investigate the mechanism of resistance to wheat (Triticum aestivum L.) powdery mildew, suppression subtractlve hybridization was conducted between an isogenic resistant line carrying Pm21 and its recurrent parent Yangmal 5 to Isolate the resistance relative genes. A cDNA fragment specifically expressed in the resistant line was obtained and its full length was cloned by in silico cloning and RT-PCR. This gene encoded a deduced protein of 219 amino acids with a leucine-rich repeat (LRR) motif, often found In plant resistance genes, and was designated as Ta-LRR2. Ta-LRR2 had an increased expression level in the resistant line after Inoculation with Erysiphe graminis DC. f. sp. tritici Marchal. PCR analysis with different cytogenetlc stocks suggested that Ta-LRR2 was specifically associated with chromosome arms 6VS and 6AS. Linkage analysis further showed that Ta-LRR2 could be used as a resistance gene analog polymorphism marker of Pm21 for marker-assisted selection in germplasm enhancement and breeding practice. Moreover, how to Isolate Pm21 based on the Information obtained for Ta-LRR2 is discussed. 展开更多
关键词 chromosome assignment molecular marker suppression subtractive hybridization (SSH) ta-lrr2 Triticum aestivumHaynaldia villosa 6VS/6AL translocation line.
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