van der Lee T, Robold A, Testa A, van 't Klooster J W, Govers F
Laboratory of Phytopathology, Wageningen University and Graduate School of Experimental Plant Sciences, Binnenhaven 9, 6709 PD Wageningen, The Netherlands.
Genetics. 2001 Mar;157(3):949-56. doi: 10.1093/genetics/157.3.949.
In this study we investigated the genetic control of avirulence in the diploid oomycete pathogen Phytophthora infestans, the causal agent of late blight on potato. The dominant avirulence (Avr) genes matched six race-specific resistance genes introgressed in potato from a wild Solanum species. AFLP markers linked to Avr genes were selected by bulked segregant analysis and used to construct two high-density linkage maps, one containing Avr4 (located on linkage group A2-a) and the other containing a cluster of three tightly linked genes, Avr3, Avr10, and Avr11 (located on linkage group VIII). Bulked segregant analysis also resulted in a marker linked to Avr1 and this allowed positioning of Avr1 on linkage group IV. No bulked segregant analysis was performed for Avr2, but linkage to a set of random markers placed Avr2 on linkage group VI. Of the six Avr genes, five were located on the most distal part of the linkage group, possibly close to the telomere. The high-density mapping was initiated to facilitate future positional cloning of P. infestans Avr genes.
在本研究中,我们调查了二倍体卵菌病原体致病疫霉(Phytophthora infestans)无毒力的遗传控制,致病疫霉是马铃薯晚疫病的病原体。显性无毒力(Avr)基因与从野生茄属物种渗入马铃薯的六个小种特异性抗性基因相匹配。通过混合分组分析法选择与Avr基因连锁的AFLP标记,并用于构建两个高密度连锁图谱,一个包含Avr4(位于连锁群A2-a上),另一个包含三个紧密连锁基因Avr3、Avr10和Avr11的簇(位于连锁群VIII上)。混合分组分析法还产生了一个与Avr1连锁的标记,这使得Avr1能够定位在连锁群IV上。未对Avr2进行混合分组分析,但与一组随机标记的连锁将Avr2定位在连锁群VI上。在这六个Avr基因中,有五个位于连锁群的最远端,可能靠近端粒。启动高密度作图是为了便于未来对致病疫霉Avr基因进行定位克隆。