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Bs2 和 Rx/Gpa2 的分段同源性支持茄科植物中抗病性的共线性。

The fractionated orthology of Bs2 and Rx/Gpa2 supports shared synteny of disease resistance in the Solanaceae.

机构信息

Department of Plant Breeding and Genetics, Cornell University, Ithaca, New York 1485, USA.

出版信息

Genetics. 2009 Aug;182(4):1351-64. doi: 10.1534/genetics.109.101022. Epub 2009 May 27.

Abstract

Comparative genomics provides a powerful tool for the identification of genes that encode traits shared between crop plants and model organisms. Pathogen resistance conferred by plant R genes of the nucleotide-binding-leucine-rich-repeat (NB-LRR) class is one such trait with great agricultural importance that occupies a critical position in understanding fundamental processes of pathogen detection and coevolution. The proposed rapid rearrangement of R genes in genome evolution would make comparative approaches tenuous. Here, we test the hypothesis that orthology is predictive of R-gene genomic location in the Solanaceae using the pepper R gene Bs2. Homologs of Bs2 were compared in terms of sequence and gene and protein architecture. Comparative mapping demonstrated that Bs2 shared macrosynteny with R genes that best fit criteria determined to be its orthologs. Analysis of the genomic sequence encompassing solanaceous R genes revealed the magnitude of transposon insertions and local duplications that resulted in the expansion of the Bs2 intron to 27 kb and the frequently detected duplications of the 5'-end of R genes. However, these duplications did not impact protein expression or function in transient assays. Taken together, our results support a conservation of synteny for NB-LRR genes and further show that their distribution in the genome has been consistent with global rearrangements.

摘要

比较基因组学为鉴定作物植物和模式生物之间共享的基因提供了强大的工具。由核苷酸结合亮氨酸丰富重复(NB-LRR)类别的植物 R 基因赋予的病原体抗性就是这样一种具有重要农业意义的性状,它在理解病原体检测和共同进化的基本过程中占有重要地位。拟议的 R 基因在基因组进化中的快速重排将使比较方法变得脆弱。在这里,我们使用辣椒 R 基因 Bs2 检验了 R 基因在茄科基因组中位置的同源性可预测的假设。根据序列和基因及蛋白质结构比较了 Bs2 的同源物。比较作图表明,Bs2 与最符合确定为其同源物的 R 基因具有宏同线性。对包含茄科 R 基因的基因组序列的分析揭示了转座子插入和局部重复的程度,导致 Bs2 内含子扩展到 27kb,并且经常检测到 R 基因 5'端的重复。然而,这些重复并没有影响瞬时测定中的蛋白质表达或功能。总之,我们的结果支持 NB-LRR 基因的同线性保守性,进一步表明它们在基因组中的分布与全局重排一致。

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