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[黑麦(Secale cereale L.)中破坏减数分裂正常进行的mei8、sy1和sy10突变的遗传分析]

[Genetic analysis of inheritance of mei8, sy1 and sy10 mutations, disrupting the correct meiosis in the rye Secale cereale L].

作者信息

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

机构信息

Department of Genetics and Breeding, St. Petersburg State University, St. Petersburg, 119034 Russia.

出版信息

Genetika. 2003 Jun;39(6):775-82.

Abstract

It is shown that mutations mei8 (irregular condensation and fragmentation of meiotic chromosomes), sy1 (asynapsis), and sy10 (heterologous synapsis) of rye Secale cereal are nonallelic. In double mutants mei8 sy1 and mei8 sy10 both mutations are expressed simultaneously and independently of each other. A study of joint inheritance of mutations sy1 and sy10 revealed their interaction by means of recessive epistasis: the double mutants has the sy10 phenotype. This means that the sy10 gene controls an earlier stage of synapsis in meiotic prophase than the sy1 gene. Mutation mei8 is inherited independently of sy1 but it is linked to sy10 (recombination frequency 26.8 +/- 3.58%).

摘要

结果表明,黑麦(Secale cereal)的突变体mei8(减数分裂染色体不规则浓缩和片段化)、sy1(不联会)和sy10(异源联会)是非等位基因。在双突变体mei8 sy1和mei8 sy10中,两种突变同时且相互独立地表达。对sy1和sy10突变联合遗传的研究揭示了它们通过隐性上位性相互作用:双突变体具有sy10表型。这意味着sy10基因在减数分裂前期控制联会的阶段比sy1基因更早。突变体mei8与sy1独立遗传,但与sy10连锁(重组频率为26.8 +/- 3.58%)。

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