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黑腹果蝇位置效应斑驳突变的比较分析确定了修饰因子的作用靶点。

Comparative analysis of position-effect variegation mutations in Drosophila melanogaster delineates the targets of modifiers.

作者信息

Sass G L, Henikoff S

机构信息

Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

出版信息

Genetics. 1998 Feb;148(2):733-41. doi: 10.1093/genetics/148.2.733.

Abstract

In Drosophila melanogaster, heterochromatin-induced silencing or position-effect variegation (PEV) of a reporter gene has provided insights into the properties of heterochromatin. Class I modifiers suppress PEV, and class II modifiers enhance PEV when the modifier gene is present in fewer than two doses. We have examined the effects of both class I and class II modifiers on four PEV mutations. These mutations include the inversions In(1)w(m4) and In(2R)bw(VDe2), which are classical chromosomal rearrangements that typify PEV mutations. The other mutations are a derivative of brown(Dominant), in which brown+ reporters are inactivated by a large block of heterochromatin, and a P[white+] transposon insertion associated with second chromosome heterochromatin. In general, we find that class I modifiers affect both classical and nonclassical PEV mutations, whereas class II modifiers affect only classical PEV mutations. We suggest that class II modifiers affect chromatin architecture in the vicinity of reporter genes, and only class I modifiers identify proteins that are potentially involved in heterochromatin formation or maintenance. In addition, our observations support a model in which there are different constraints on the process of heterochromatin-induced silencing in classical vs. nonclassical PEV mutations.

摘要

在黑腹果蝇中,报告基因的异染色质诱导沉默或位置效应斑驳(PEV)为深入了解异染色质的特性提供了线索。I类修饰因子抑制PEV,而当修饰基因的剂量少于两个时,II类修饰因子增强PEV。我们研究了I类和II类修饰因子对四种PEV突变的影响。这些突变包括倒位In(1)w(m4)和In(2R)bw(VDe2),它们是典型的代表PEV突变的经典染色体重排。其他突变是棕色(显性)的衍生物,其中棕色+报告基因被一大块异染色质失活,以及与第二条染色体异染色质相关的P[白色+]转座子插入。一般来说,我们发现I类修饰因子影响经典和非经典PEV突变,而II类修饰因子只影响经典PEV突变。我们认为II类修饰因子影响报告基因附近的染色质结构,只有I类修饰因子能识别可能参与异染色质形成或维持的蛋白质。此外,我们的观察结果支持一种模型,即在经典与非经典PEV突变中,异染色质诱导沉默过程存在不同的限制。

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