Grimaud Charlotte, Nègre Nicolas, Cavalli Giacomo
Institute of Human Genetics, CNRS, 141, rue de la Cardonille, 34396, Montpellier Cedex 5, France.
Chromosome Res. 2006;14(4):363-75. doi: 10.1007/s10577-006-1069-y.
The Polycomb gene was discovered 60 years ago as a mutation inducing a particular homeotic phenotype. Subsequent work showed that Polycomb is a general repressor of homeotic genes. Other genes with similar function were identified and named Polycomb group (PcG) genes, while trithorax group (trxG) genes were shown to counteract PcG-mediated repression of homeotic genes. We now know that PcG and trxG proteins are conserved factors that regulate hundreds of different genomic loci. A sophisticated pathway is responsible for recruitment of these proteins at regulatory regions that were named PcG and trxG response elements (PRE and TRE). Once recruited to their targets, multimeric PcG and trxG protein complexes regulate transcription by modulating chromatin structure, in particular via deposition of specific post-translational histone modification marks and control of chromatin accessibility, as well as regulation of the three-dimensional nuclear organization of PRE and TRE. Here, we recapitulate the history of PcG and trxG gene discovery, we review the current evidence on their molecular function and, based on this evidence, we propose a revised classification of genes involved in PcG and trxG regulatory pathways.
60年前,多梳基因作为一种诱导特定同源异型表型的突变被发现。随后的研究表明,多梳蛋白是同源异型基因的一般抑制因子。其他具有相似功能的基因被鉴定并命名为多梳家族(PcG)基因,而三胸节家族(trxG)基因则被证明可对抗PcG介导的同源异型基因抑制作用。我们现在知道,PcG和trxG蛋白是保守因子,可调控数百个不同的基因组位点。一个复杂的途径负责将这些蛋白招募到被称为PcG和trxG反应元件(PRE和TRE)的调控区域。一旦被招募到其靶标,多聚体PcG和trxG蛋白复合物通过调节染色质结构来调控转录,特别是通过特定翻译后组蛋白修饰标记的沉积和染色质可及性的控制,以及PRE和TRE的三维核组织的调节。在这里,我们概述了PcG和trxG基因的发现历史,回顾了关于它们分子功能的当前证据,并基于此证据提出了参与PcG和trxG调控途径的基因的修订分类。