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黑腹果蝇中修饰基因与可修饰等位基因的遗传相互作用。

Genetic interactions of modifier genes and modifiable alleles in Drosophila melanogaster.

作者信息

Rutledge B J, Mortin M A, Schwarz E, Thierry-Mieg D, Meselson M

机构信息

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138.

出版信息

Genetics. 1988 Jun;119(2):391-7. doi: 10.1093/genetics/119.2.391.

Abstract

We have examined the effects of mutations in the six allele-specific modifier genes su(Hw), e(we), su(f), su(s), su(wa), and su(pr) on the expression of 18 modifiable alleles, situated at 11 loci. Ten of the modifiable alleles are associated with insertions of the gypsy retrotransposon and the others include alleles associated with insertions of copia and 412. We tested or retested 90 of the 108 possible combinations and examined the expression of modifiable alleles in flies mutant for pairs of modifier genes in various heterozygous and homozygous configurations. Our principal findings are: (1) a screen of 40,000 mutagenized X chromosomes yielded three new mutations in known modifier genes, but revealed no new modifier genes; (2) the modification effects of different mutations in a given modifier gene were qualitatively similar; (3) each of the six modifiers suppressed some modifiable alleles, enhanced others, and had no noticeable effect on still others; (4) the modifier genes could be placed in four classes, according to their effects on the gypsy-insertion alleles; and (5) the effects of mutations in different modifier genes combined additively. Implications of these results for models of modifier gene action are discussed.

摘要

我们研究了六个等位基因特异性修饰基因su(Hw)、e(we)、su(f)、su(s)、su(wa)和su(pr)中的突变对位于11个位点的18个可修饰等位基因表达的影响。其中10个可修饰等位基因与gypsy逆转座子的插入有关,其他等位基因包括与copia和412插入有关的等位基因。我们测试或重新测试了108种可能组合中的90种,并检查了处于各种杂合和纯合构型的修饰基因对突变果蝇中可修饰等位基因的表达情况。我们的主要发现如下:(1) 对40,000条诱变X染色体进行筛选,在已知修饰基因中产生了三个新突变,但未发现新的修饰基因;(2) 给定修饰基因中不同突变的修饰效果在质量上相似;(3) 六个修饰基因中的每一个都抑制了一些可修饰等位基因,增强了其他等位基因,而对其他一些等位基因没有明显影响;(4) 根据修饰基因对gypsy插入等位基因的影响,可将其分为四类;(5) 不同修饰基因中的突变效应组合具有加性。本文讨论了这些结果对修饰基因作用模型的意义。

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