普通小麦Lr19易位杀配子体效应的遗传研究

R. Prins, G. F. Marais
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引用次数: 23

摘要

由于至少两个基因Sd1和Sd2(新名称)的作用,Lr19易位优先传递给杂合子的后代。然而,只有Sd2出现在重组基因Lr19-149中,并且经常导致杂合子中重组易位片段的自我消除。分离畸变的程度是由Sd基因与不同染色体上的多基因(应答基因)相互作用决定的。在本研究中,来自“印度66”或“印度”的疑似应答等位基因(染色体2A、2B、3B、5B、5D和6D)与来自“中国春”的等位基因相比,大部分表现为部分显性或超显性。一个特定的等位基因在不同的遗传背景下不一定具有相同的作用(抑制或增强)。响应基因可能不能完全补偿半合子中同源基因的缺失,这可能会产生与同合子和杂合子完全不同的效果。
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A genetic study of the gametocidal effect of the Lr19 translocation of common wheat
The Lr19 translocation is preferentially transmitted to the progeny of a heterozygote due to the actions of at least two genes, Sd1 and Sd2 (new designation). However, only Sd2 occurs in the recombinant, Lr19-149, and often causes self-elimination of the recombined translocated segment in heterozygotes. The degree of segregation distortion is determined by the interaction of the Sd genes with polygenes (responder genes) on various wheat chromosomes. In this study suspected responder alleles derived from ‘Inia 66’ or ‘Indis’ (chromosomes 2A, 2B, 3B, 5B, 5D and 6D) appeared mostly to be partially dominant to overdominant over the ‘Chinese Spring’ derived alleles. A specific allele may not necessarily hafe-tfoe same effect (suppression or enhancement) in different genetic backgrounds. Responder genes may not fully compensate for the absence of a homologue in a hemizygote which may then produce effects quite different from those of the homo- and heterozygotes.
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