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果蝇的雄性特异性致死复合体将X染色体的活化区域作为染色质重塑的靶点。

Male-specific lethal complex of Drosophila targets activated regions of the X chromosome for chromatin remodeling.

作者信息

Sass Georgette L, Pannuti Antonio, Lucchesi John C

机构信息

Department of Biology, Emory University, 1510 Clifton Road, Atlanta, GA 30322, USA.

出版信息

Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8287-91. doi: 10.1073/pnas.1332749100. Epub 2003 Jun 26.

Abstract

The male-specific lethal (MSL) complex of Drosophila is responsible for the presence of a monoacetylated isoform of histone H4 (H4Ac16), found exclusively on the X chromosome of males. This particular covalent modification of histone H4 is correlated with a 2-fold enhancement of the transcription of most X-linked genes in Drosophila males, which is the basis of dosage compensation in this organism. Although widespread along the X chromosome, the MSL complex is not distributed uniformly, as can be seen by the indirect cytoimmunofluorescence staining of larval salivary-gland polytene chromosomes. This distribution pattern has been interpreted as a reflection of the tissue-specific transcriptional activity of the larval salivary gland and as an indication that the MSL complex associates with active chromatin. We have tested this hypothesis by comparing the chromosomal distribution of the complex in two different tissues. We performed this comparison by following the pattern of association of the complex at a specific site on salivary-gland chromosomes during larval development and determining whether an ectopic promoter located in a complex-devoid region of the X chromosome is able to attract the complex upon activation. Our results indicate that, in contrast to other chromatin-remodeling complexes that enhance transcription, the MSL complex targets active chromatin.

摘要

果蝇的雄性特异性致死(MSL)复合体导致了组蛋白H4单乙酰化异构体(H4Ac16)的存在,该异构体仅在雄性果蝇的X染色体上被发现。组蛋白H4的这种特定共价修饰与果蝇雄性中大多数X连锁基因转录增强2倍相关,这是该生物体剂量补偿的基础。尽管MSL复合体在X染色体上广泛分布,但通过幼虫唾液腺多线染色体的间接细胞免疫荧光染色可以看出,它并非均匀分布。这种分布模式被解释为幼虫唾液腺组织特异性转录活性的反映,也表明MSL复合体与活性染色质相关联。我们通过比较该复合体在两种不同组织中的染色体分布来检验这一假设。我们通过追踪幼虫发育过程中该复合体在唾液腺染色体上特定位点的结合模式,并确定位于X染色体复合体缺失区域的异位启动子在激活后是否能够吸引该复合体,进行了此项比较。我们的结果表明,与其他增强转录的染色质重塑复合体不同,MSL复合体靶向活性染色质。

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