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[导致二倍体黑麦(Secale cereale L.)染色体中非同源减数分裂联会的突变体sy2的遗传分析]

[Genetic analysis of mutation sy2 which causes nonhomologous meiotic synapsis in chromosomes of diploid rye Secale cereale L].

作者信息

Sosnokhina S P, Kirillova G A, Tikholiz O A, Mikhaĭlova E I, Priiatkina S N, Smirnov V G

机构信息

Department of Genetics and Breeding, St. Petersburg State University, St. Petersubrg, 199034 Russia.

出版信息

Genetika. 2002 Mar;38(3):347-56.

Abstract

Partially nonhomologous (heterologous) synapsis of meiotic chromosomes in a spontaneous desynaptic mutant form of rye is determined by two recessive genes, sy2a and sy2b, that have independent expression and inheritance. The third gene, dominant inhibitor suppressing the mutant phenotype, has been revealed in hybrid combinations between sy2 mutants and lines segregating other meiotic mutants: sy10 (heterologous synapsis), sy1, and sy9 (asynapsis). All three genes determining desynapsis (sy2a, sy2b, and I) were shown to be nonallelic to monogenic mutations sy10, sy1, and sy9, inherited independently of them and expressed at later stages of prophase I than the sy10 gene. The possibility of modifying monogenic segregation of mutation sy2 by gametophyte selection for a locus linked to the gene expressed as sy2 at particular frequencies of recombination between this gene and selected locus is discussed.

摘要

在黑麦的一种自发去联会突变体形式中,减数分裂染色体的部分非同源(异源)联会由两个隐性基因sy2a和sy2b决定,它们具有独立的表达和遗传方式。在sy2突变体与分离其他减数分裂突变体(sy10(异源联会)、sy1和sy9(不联会))的品系之间的杂交组合中,发现了第三个基因,即抑制突变体表型的显性抑制剂。决定去联会的所有三个基因(sy2a、sy2b和I)被证明与单基因突sy10、sy1和sy9非等位,独立于它们遗传,并且在前期I的后期表达,比sy10基因表达得晚。本文讨论了通过配子体选择针对与该基因以特定重组频率表现为sy2的基因座来修饰突变sy2的单基因分离的可能性。

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