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普通小麦中抑制基因Igc1与杀配子基因Gc3 - C1的分子定位

Molecular mapping of the suppressor gene Igc1 to the gametocidal gene Gc3-C1 in common wheat.

作者信息

Yamano Soichi, Nitta Miyuki, Tsujimoto Hisashi, Ishikawa Goro, Nakamura Toshiki, Endo Takashi R, Nasuda Shuhei

机构信息

Laboratory of Plant Genetics, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Genes Genet Syst. 2010 Feb;85(1):43-53. doi: 10.1266/ggs.85.43.

Abstract

Several species of the genus Aegilops, wild relatives of wheat (Triticum aestivum, 2n = 6x = 42, AABBDD) carry gametocidal (Gc) genes. Gc genes kill the gametes without themselves by causing chromosomal breakage during post-meiotic cell divisions, and therefore are strong segregation distorters. The Gc gene Gc3-C1 derived from chromosome 3C of Ae. triuncialis (2n = 4x = 28, CCUU) induces chromosomal breakage in wheat cultivar 'Chinese Spring' (CS) but not in cultivar 'Norin 26' (N26). This cultivar-specific inhibition of Gc function is caused by a suppressor gene Igc1 located on chromosome 3B of N26. Igc1 is presumed to be a modified Gc gene without breakage function because of its homoeology to Gc3-C1. Here we report the results of linkage and physical mapping of Igc1 to help elucidate the molecular mechanisms underlying Gc action. Segregation analysis of the phenotypic data in BC(1)F(1) mapping population of the cross between (CSxN26)F(1) and CS + 3C" showed a 1:1 segregation ratio indicating that Igc1 is a dominant gene. In the linkage analysis, three molecular marker loci Xgwm285, Xgwm376, and Xcfp1886 cosegregated with the Igc1 locus. Bin mapping assigned the loci Xgwm285 and Xcfp1886 to bin C-3BS1-0.33 and Xgwm376 to bin C-3BL2-0.22. Physical mapping using Gc-induced chromosomal deletion lines of chromosome 3B of N26 revealed that the Igc1 locus resides in 52.0% or 2.1% of bins C-3BS1-0.33 and C-3BL2-0.22, respectively. Pericentromeric localization of Igc1 in chromosome 3B of N26 may have a positive effect to keep the two-component system of the Gc action. Map-based cloning approach to isolate the Igc1 may be difficult because recombination is depleted in the pericentromeric region. As is shown in this study, the combination of genetic and physical mapping offers high efficiency to identify the regions where genes are located especially in regions with low levels of recombination.

摘要

山羊草属的几个物种是小麦(普通小麦,2n = 6x = 42,AABBDD)的野生近缘种,携带杀配子(Gc)基因。Gc基因通过在减数分裂后细胞分裂期间引起染色体断裂来杀死配子,因此是强烈的分离畸变因子。源自节节麦(2n = 4x = 28,CCUU)3C染色体的Gc基因Gc3-C1在小麦品种“中国春”(CS)中诱导染色体断裂,但在品种“Norin 26”(N26)中不诱导。N26中位于3B染色体上的抑制基因Igc1导致了这种品种特异性的Gc功能抑制。由于Igc1与Gc3-C1的同源性,推测它是一个没有断裂功能的修饰Gc基因。在此,我们报告Igc1的连锁和物理图谱绘制结果,以帮助阐明Gc作用的分子机制。对(CSxN26)F1与CS + 3C”杂交的BC(1)F(1)作图群体的表型数据进行分离分析,显示分离比为1:1,表明Igc1是一个显性基因。在连锁分析中,三个分子标记位点Xgwm285、Xgwm376和Xcfp1886与Igc1位点共分离。染色体区域定位将位点Xgwm285和Xcfp1886定位到C-3BS1-0.33区域,将Xgwm376定位到C-3BL2-0.22区域。使用N26 3B染色体的Gc诱导染色体缺失系进行物理图谱绘制表明,Igc1位点分别位于C-3BS1-0.33和C-3BL2-0.22区域的52.0%或2.1%处。Igc1在N26 3B染色体上的着丝粒周围定位可能对维持Gc作用的双组分系统有积极作用。基于图谱的克隆方法分离Igc1可能很困难,因为着丝粒周围区域的重组很少。如本研究所示,遗传图谱和物理图谱相结合能够高效地鉴定基因所在区域,尤其是在重组水平较低的区域。

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