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本文引用的文献

1
The blast resistance gene Pi37 encodes a nucleotide binding site leucine-rich repeat protein and is a member of a resistance gene cluster on rice chromosome 1.抗稻瘟病基因Pi37编码一种核苷酸结合位点富含亮氨酸重复序列的蛋白,是水稻第1号染色体上一个抗病基因簇的成员。
Genetics. 2007 Nov;177(3):1871-80. doi: 10.1534/genetics.107.080648. Epub 2007 Oct 18.
2
The in silico map-based cloning of Pi36, a rice coiled-coil nucleotide-binding site leucine-rich repeat gene that confers race-specific resistance to the blast fungus.基于电子图谱克隆水稻卷曲螺旋核苷酸结合位点富含亮氨酸重复序列基因Pi36,该基因赋予对稻瘟病菌的小种特异性抗性。
Genetics. 2007 Aug;176(4):2541-9. doi: 10.1534/genetics.107.075465. Epub 2007 May 16.
3
The genomic dynamics and evolutionary mechanism of the Pi2/9 locus in rice.水稻中Pi2/9基因座的基因组动态变化及进化机制
Mol Plant Microbe Interact. 2007 Jan;20(1):63-71. doi: 10.1094/MPMI-20-0063.
4
Plant NBS-LRR proteins in pathogen sensing and host defense.植物NBS-LRR蛋白在病原体感知和宿主防御中的作用
Nat Immunol. 2006 Dec;7(12):1243-9. doi: 10.1038/ni1410.
5
The eight amino-acid differences within three leucine-rich repeats between Pi2 and Piz-t resistance proteins determine the resistance specificity to Magnaporthe grisea.Pi2和Piz-t抗性蛋白之间三个富含亮氨酸重复序列中的八个氨基酸差异决定了对稻瘟病菌的抗性特异性。
Mol Plant Microbe Interact. 2006 Nov;19(11):1216-28. doi: 10.1094/MPMI-19-1216.
6
The tomato NBARC-LRR protein Prf interacts with Pto kinase in vivo to regulate specific plant immunity.番茄NBARC-LRR蛋白Prf在体内与Pto激酶相互作用,以调节特定的植物免疫。
Plant Cell. 2006 Oct;18(10):2792-806. doi: 10.1105/tpc.106.044016. Epub 2006 Oct 6.
7
Development of PCR-based allele-specific and InDel marker sets for nine rice blast resistance genes.用于九个水稻抗稻瘟病基因的基于PCR的等位基因特异性和插入缺失标记集的开发。
Theor Appl Genet. 2006 Jul;113(2):251-60. doi: 10.1007/s00122-006-0290-6. Epub 2006 May 4.
8
Resistance proteins: molecular switches of plant defence.抗性蛋白:植物防御的分子开关
Curr Opin Plant Biol. 2006 Aug;9(4):383-90. doi: 10.1016/j.pbi.2006.05.009. Epub 2006 May 19.
9
A B-lectin receptor kinase gene conferring rice blast resistance.一个赋予水稻稻瘟病抗性的B-凝集素受体激酶基因。
Plant J. 2006 Jun;46(5):794-804. doi: 10.1111/j.1365-313X.2006.02739.x.
10
The broad-spectrum blast resistance gene Pi9 encodes a nucleotide-binding site-leucine-rich repeat protein and is a member of a multigene family in rice.广谱抗稻瘟病基因Pi9编码一种核苷酸结合位点富含亮氨酸重复序列的蛋白,是水稻中一个多基因家族的成员。
Genetics. 2006 Mar;172(3):1901-14. doi: 10.1534/genetics.105.044891. Epub 2005 Dec 30.

两个相邻的核苷酸结合位点富含亮氨酸重复序列类基因是赋予Pikm特异性抗稻瘟病能力所必需的。

Two adjacent nucleotide-binding site-leucine-rich repeat class genes are required to confer Pikm-specific rice blast resistance.

作者信息

Ashikawa Ikuo, Hayashi Nagao, Yamane Hiroko, Kanamori Hiroyuki, Wu Jianzhong, Matsumoto Takashi, Ono Kazuko, Yano Masahiro

机构信息

QTL Genomics Research Center, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.

出版信息

Genetics. 2008 Dec;180(4):2267-76. doi: 10.1534/genetics.108.095034. Epub 2008 Oct 20.

DOI:10.1534/genetics.108.095034
PMID:18940787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2600957/
Abstract

The rice blast resistance gene Pikm was cloned by a map-based cloning strategy. High-resolution genetic mapping and sequencing of the gene region in the Pikm-containing cultivar Tsuyuake narrowed down the candidate region to a 131-kb genomic interval. Sequence analysis predicted two adjacently arranged resistance-like genes, Pikm1-TS and Pikm2-TS, within this candidate region. These genes encoded proteins with a nucleotide-binding site (NBS) and leucine-rich repeats (LRRs) and were considered the most probable candidates for Pikm. However, genetic complementation analysis of transgenic lines individually carrying these two genes negated the possibility that either Pikm1-TS or Pikm2-TS alone was Pikm. Instead, it was revealed that transgenic lines carrying both of these genes expressed blast resistance. The results of the complementation analysis and an evaluation of the resistance specificity of the transgenic lines to blast isolates demonstrated that Pikm-specific resistance is conferred by cooperation of Pikm1-TS and Pikm2-TS. Although these two genes are not homologous with each other, they both contain all the conserved motifs necessary for an NBS-LRR class gene to function independently as a resistance gene.

摘要

通过图位克隆策略克隆了水稻抗稻瘟病基因Pikm。对含有Pikm的品种津轻早生中该基因区域进行高分辨率遗传定位和测序,将候选区域缩小到一个131 kb的基因组区间。序列分析预测在该候选区域内有两个相邻排列的类抗性基因,即Pikm1-TS和Pikm2-TS。这些基因编码具有核苷酸结合位点(NBS)和富含亮氨酸重复序列(LRR)的蛋白质,被认为是Pikm最有可能的候选基因。然而,对单独携带这两个基因的转基因系进行的遗传互补分析排除了Pikm1-TS或Pikm2-TS单独为Pikm的可能性。相反,结果表明携带这两个基因的转基因系表现出稻瘟病抗性。互补分析结果以及对转基因系对稻瘟病菌株抗性特异性的评估表明,Pikm特异性抗性是由Pikm1-TS和Pikm2-TS共同作用赋予的。尽管这两个基因彼此不具有同源性,但它们都包含NBS-LRR类基因独立作为抗性基因发挥功能所需的所有保守基序。