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Variegation in Drosophila and the Inert Chromosome Regions.果蝇中的斑纹现象与惰性染色体区域
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The dichotornous action of Y chromosomes on the expression of position-effect variegation.Y染色体对位置效应斑驳表达的二分作用。
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Modification of the Drosophila heterochromatic mutation brownDominant by linkage alterations.通过连锁改变对果蝇异染色质突变brownDominant的修饰。
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Looking at Drosophila mitotic chromosomes.观察果蝇有丝分裂染色体。
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异染色质对黑腹果蝇异染色质和常染色质基因活性的顺式效应。

Cis-effects of heterochromatin on heterochromatic and euchromatic gene activity in Drosophila melanogaster.

作者信息

Howe M, Dimitri P, Berloco M, Wakimoto B T

机构信息

Department of Zoology, University of Washington, Seattle 98195-1800, USA.

出版信息

Genetics. 1995 Jul;140(3):1033-45. doi: 10.1093/genetics/140.3.1033.

DOI:10.1093/genetics/140.3.1033
PMID:7672575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1206659/
Abstract

Chromosomal rearrangements that juxtapose heterochromatin and euchromatin can result in mosaic inactivation of heterochromatic and euchromatic genes. This phenomenon, position effect variegation (PEV), suggests that heterochromatic and euchromatic genes differ in their regulatory requirements. This report describes a novel method for mapping regions required for heterochromatic genes, and those that induce PEV of a euchromatic gene. P transposase mutagenesis was used to generate derivatives of a translocation that variegated for the light+ (lt+) gene and carried the euchromatic white+ (w+) gene on a transposon near the heterochromatin-euchromatin junction. Cytogenetic and genetic analyses of the derivatives showed that P mutagenesis resulted in deletions of several megabases of heterochromatin. Genetic and molecular studies showed that the derivatives shared a euchromatic breakpoint but differed in their heterochromatic breakpoint and their effects on seven heterochromatic genes and the w+ gene. Heterochromatic genes differed in their response to deletions. The lt+ gene was sensitive to the amount of heterochromatin at the breakpoint but the heterochromatic 40Fa gene was not. The severity of variegated w+ phenotype did not depend on the amount of heterochromatin in cis, but varied with local heterochromatic environment. These data are relevant for considering mechanisms of PEV of both heterochromatic and euchromatic genes.

摘要

使异染色质和常染色质并列的染色体重排可导致异染色质和常染色质基因的镶嵌失活。这种现象,即位置效应斑驳(PEV),表明异染色质和常染色质基因在调控需求上存在差异。本报告描述了一种用于绘制异染色质基因所需区域以及那些诱导常染色质基因发生PEV的区域的新方法。利用P转座酶诱变产生了一种易位的衍生物,该易位对于光+(lt+)基因表现出斑驳现象,并在异染色质 - 常染色质交界处附近的转座子上携带常染色质白色+(w+)基因。对这些衍生物进行细胞遗传学和遗传学分析表明,P诱变导致了几个百万碱基的异染色质缺失。遗传学和分子研究表明,这些衍生物共享一个常染色质断点,但在异染色质断点以及它们对七个异染色质基因和w+基因的影响方面存在差异。异染色质基因对缺失的反应各不相同。lt+基因对断点处异染色质的量敏感,但异染色质40Fa基因则不敏感。斑驳的w+表型的严重程度并不取决于顺式异染色质的量,而是随局部异染色质环境而变化。这些数据对于考虑异染色质和常染色质基因的PEV机制具有重要意义。