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尖叶蕉中非TIR NBS-LRR抗性基因类似物的分析:分离、RFLP标记开发及物理图谱构建

Analysis of non-TIR NBS-LRR resistance gene analogs in Musa acuminata Colla: isolation, RFLP marker development, and physical mapping.

作者信息

Miller Robert N G, Bertioli David J, Baurens Franc C, Santos Candice M R, Alves Paulo C, Martins Natalia F, Togawa Roberto C, Souza Manoel T, Pappas Georgios J

机构信息

Postgraduate program in Genomic Science and Biotechnology, Universidade Católica de Brasília, SGAN 916, Módulo B, CEP 70,790-160, Brasília, DF, Brazil.

出版信息

BMC Plant Biol. 2008 Jan 30;8:15. doi: 10.1186/1471-2229-8-15.

Abstract

BACKGROUND

Many commercial banana varieties lack sources of resistance to pests and diseases, as a consequence of sterility and narrow genetic background. Fertile wild relatives, by contrast, possess greater variability and represent potential sources of disease resistance genes (R-genes). The largest known family of plant R-genes encode proteins with nucleotide-binding site (NBS) and C-terminal leucine-rich repeat (LRR) domains. Conserved motifs in such genes in diverse plant species offer a means for isolation of candidate genes in banana which may be involved in plant defence.

RESULTS

A computational strategy was developed for unbiased conserved motif discovery in NBS and LRR domains in R-genes and homologues in monocotyledonous plant species. Degenerate PCR primers targeting conserved motifs were tested on the wild cultivar Musa acuminata subsp. burmannicoides, var. Calcutta 4, which is resistant to a number of fungal pathogens and nematodes. One hundred and seventy four resistance gene analogs (RGAs) were amplified and assembled into 52 contiguous sequences. Motifs present were typical of the non-TIR NBS-LRR RGA subfamily. A phylogenetic analysis of deduced amino-acid sequences for 33 RGAs with contiguous open reading frames (ORFs), together with RGAs from Arabidopsis thaliana and Oryza sativa, grouped most Musa RGAs within monocotyledon-specific clades. RFLP-RGA markers were developed, with 12 displaying distinct polymorphisms in parentals and F1 progeny of a diploid M. acuminata mapping population. Eighty eight BAC clones were identified in M. acuminata Calcutta 4, M. acuminata Grande Naine, and M. balbisiana Pisang Klutuk Wulung BAC libraries when hybridized to two RGA probes. Multiple copy RGAs were common within BAC clones, potentially representing variation reservoirs for evolution of new R-gene specificities.

CONCLUSION

This is the first large scale analysis of NBS-LRR RGAs in M. acuminata Calcutta 4. Contig sequences were deposited in GenBank and assigned numbers ER935972 - ER936023. RGA sequences and isolated BACs are a valuable resource for R-gene discovery, and in future applications will provide insight into the organization and evolution of NBS-LRR R-genes in the Musa A and B genome. The developed RFLP-RGA markers are applicable for genetic map development and marker assisted selection for defined traits such as pest and disease resistance.

摘要

背景

由于不育性和狭窄的遗传背景,许多商业香蕉品种缺乏对病虫害的抗性来源。相比之下,可育的野生近缘种具有更大的变异性,是抗病基因(R基因)的潜在来源。已知最大的植物R基因家族编码具有核苷酸结合位点(NBS)和C端富含亮氨酸重复序列(LRR)结构域的蛋白质。不同植物物种中此类基因的保守基序为分离香蕉中可能参与植物防御的候选基因提供了一种方法。

结果

开发了一种计算策略,用于在单子叶植物物种的R基因及其同源物的NBS和LRR结构域中无偏地发现保守基序。针对保守基序设计的简并PCR引物在野生品种尖叶蕉亚种(Musa acuminata subsp. burmannicoides)、变种加尔各答4号(var. Calcutta 4)上进行了测试,该品种对多种真菌病原体和线虫具有抗性。扩增出174个抗病基因类似物(RGA),并组装成52个连续序列。存在的基序是典型的非TIR NBS-LRR RGA亚家族的基序。对33个具有连续开放阅读框(ORF)的RGA以及来自拟南芥和水稻的RGA推导的氨基酸序列进行系统发育分析,将大多数香蕉RGA归入单子叶植物特有的进化枝中。开发了RFLP-RGA标记,其中12个在二倍体尖叶蕉作图群体的亲本和F1后代中表现出明显的多态性。当与两个RGA探针杂交时,在尖叶蕉加尔各答4号、尖叶蕉大奈(M. acuminata Grande Naine)和野蕉(M. balbisiana Pisang Klutuk Wulung)BAC文库中鉴定出88个BAC克隆。BAC克隆中常见多拷贝RGA,可能代表新R基因特异性进化的变异库。

结论

这是对尖叶蕉加尔各答4号中NBS-LRR RGA的首次大规模分析。重叠群序列已存入GenBank,并被赋予编号ER935972 - ER936023。RGA序列和分离的BAC是R基因发现的宝贵资源,在未来的应用中将有助于深入了解香蕉A和B基因组中NBS-LRR R基因的组织和进化。开发的RFLP-RGA标记适用于遗传图谱构建以及对病虫害抗性等特定性状的标记辅助选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/401f/2262081/85716aa5ea7e/1471-2229-8-15-1.jpg

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