Genome-Wide Architecture of Disease Resistance Genes in Lettuce

被引:45
|
作者
Christopoulou, Marilena
Wo, Sebastian Reyes-Chin
Kozik, Alex
McHale, Leah K.
Truco, Maria-Jose
Wroblewski, Tadeusz
Michelmore, Richard W. [1 ]
机构
[1] Univ Calif Davis, Genome Ctr, Davis, CA 95616 USA
来源
G3-GENES GENOMES GENETICS | 2015年 / 5卷 / 12期
基金
美国国家科学基金会;
关键词
reverse genetics; NB-LRR; lettuce downy mildew; gene silencing; Bremia lactucae; LEUCINE-RICH REPEAT; NUCLEOTIDE-BINDING SITE; LRR-ENCODING GENES; LACTUCA-SATIVA; PROTEIN TOPOLOGY; BREMIA-LACTUCAE; MAJOR CLUSTER; PLANT; EVOLUTION; IDENTIFICATION;
D O I
10.1534/g3.115.020818
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome-wide motif searches identified 1134 genes in the lettuce reference genome of cv. Salinas that are potentially involved in pathogen recognition, of which 385 were predicted to encode nucleotide binding-leucine rich repeat receptor (NLR) proteins. Using a maximum-likelihood approach, we grouped the NLRs into 25 multigene families and 17 singletons. Forty-one percent of these NLR-encoding genes belong to three families, the largest being RGC16 with 62 genes in cv. Salinas. The majority of NLR-encoding genes are located in five major resistance clusters (MRCs) on chromosomes 1, 2, 3, 4, and 8 and cosegregate with multiple disease resistance phenotypes. Most MRCs contain primarily members of a single NLR gene family but a few are more complex. MRC2 spans 73 Mb and contains 61 NLRs of six different gene families that cosegregate with nine disease resistance phenotypes. MRC3, which is 25 Mb, contains 22 RGC21 genes and colocates with Dm13. A library of 33 transgenic RNA interference tester stocks was generated for functional analysis of NLR-encoding genes that cosegregated with disease resistance phenotypes in each of the MRCs. Members of four NLR-encoding families, RGC1, RGC2, RGC21, and RGC12 were shown to be required for 16 disease resistance phenotypes in lettuce. The general composition of MRCs is conserved across different genotypes; however, the specific repertoire of NLR-encoding genes varied particularly of the rapidly evolving Type I genes. These tester stocks are valuable resources for future analyses of additional resistance phenotypes.
引用
收藏
页码:2655 / 2669
页数:15
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