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果蝇多梳蛋白组抑制中腿上性梳蛋白相互作用的要求

Requirement for sex comb on midleg protein interactions in Drosophila polycomb group repression.

作者信息

Peterson Aidan J, Mallin Daniel R, Francis Nicole J, Ketel Carrie S, Stamm Joyce, Voeller Rochus K, Kingston Robert E, Simon Jeffrey A

机构信息

Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota 55455, USA.

出版信息

Genetics. 2004 Jul;167(3):1225-39. doi: 10.1534/genetics.104.027474.

Abstract

The Drosophila Sex Comb on Midleg (SCM) protein is a transcriptional repressor of the Polycomb group (PcG). Although genetic studies establish SCM as a crucial PcG member, its molecular role is not known. To investigate how SCM might link to PcG complexes, we analyzed the in vivo role of a conserved protein interaction module, the SPM domain. This domain is found in SCM and in another PcG protein, Polyhomeotic (PH), which is a core component of Polycomb repressive complex 1 (PRC1). SCM-PH interactions in vitro are mediated by their respective SPM domains. Yeast two-hybrid and in vitro binding assays were used to isolate and characterize >30 missense mutations in the SPM domain of SCM. Genetic rescue assays showed that SCM repressor function in vivo is disrupted by mutations that impair SPM domain interactions in vitro. Furthermore, overexpression of an isolated, wild-type SPM domain produced PcG loss-of-function phenotypes in flies. Coassembly of SCM with a reconstituted PRC1 core complex shows that SCM can partner with PRC1. However, gel filtration chromatography showed that the bulk of SCM is biochemically separable from PH in embryo nuclear extracts. These results suggest that SCM, although not a core component of PRC1, interacts and functions with PRC1 in gene silencing.

摘要

果蝇中腿上的性梳(SCM)蛋白是多梳蛋白组(PcG)的一种转录抑制因子。尽管遗传学研究确定SCM是PcG的关键成员,但其分子作用尚不清楚。为了研究SCM如何与PcG复合物联系,我们分析了一个保守的蛋白质相互作用模块——SPM结构域在体内的作用。该结构域存在于SCM和另一种PcG蛋白多同源蛋白(PH)中,PH是多梳抑制复合物1(PRC1)的核心成分。SCM与PH在体外的相互作用是由它们各自的SPM结构域介导的。利用酵母双杂交和体外结合试验分离并鉴定了SCM的SPM结构域中的30多个错义突变。基因拯救试验表明,体内SCM的抑制功能会被体外损害SPM结构域相互作用的突变所破坏。此外,单独的野生型SPM结构域的过表达在果蝇中产生了PcG功能丧失的表型。SCM与重组的PRC1核心复合物的共组装表明SCM可以与PRC1结合。然而,凝胶过滤色谱显示,在胚胎核提取物中,大部分SCM在生化性质上可与PH分离。这些结果表明,SCM虽然不是PRC1的核心成分,但在基因沉默中与PRC1相互作用并发挥功能。

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