Stankunas K, Berger J, Ruse C, Sinclair D A, Randazzo F, Brock H W
Department of Zoology, University of British Columbia, Vancouver, BC, Canada, V6T 1Z4.
Development. 1998 Oct;125(20):4055-66. doi: 10.1242/dev.125.20.4055.
The Polycomb group of genes in Drosophila are homeotic switch gene regulators that maintain homeotic gene repression through a possible chromatin regulatory mechanism. The Enhancer of Polycomb (E(Pc)) gene of Drosophila is an unusual member of the Polycomb group. Most PcG genes have homeotic phenotypes and are required for repression of homeotic loci, but mutations in E(Pc) exhibit no homeotic transformations and have only a very weak effect on expression of Abd-B. However, mutations in E(Pc) are strong enhancers of mutations in many Polycomb group genes and are also strong suppressors of position-effect variegation, suggesting that E(Pc) may have a wider role in chromatin formation or gene regulation than other Polycomb group genes. E(Pc) was cloned by transposon tagging, and encodes a novel 2023 amino acid protein with regions enriched in glutamine, alanine and asparagine. E(Pc) is expressed ubiquitously in Drosophila embryogenesis. E(Pc) is a chromatin protein, binding to polytene chromosomes at about 100 sites, including the Antennapedia but not the Bithorax complex, 29% of which are shared with Polycomb-binding sites. Surprisingly, E(Pc) was not detected in the heterochromatic chromocenter. This result suggests that E(Pc) has a functional rather than structural role in heterochromatin formation and argues against the heterochromatin model for PcG function. Using homology cloning techniques, we identified a mouse homologue of E(Pc), termed Epc1, a yeast protein that we name EPL1, and as well as additional ESTs from Caenorhabditis elegans, mice and humans. Epc1 shares a long, highly conserved domain in its amino terminus with E(Pc) that is also conserved in yeast, C. elegans and humans. The occurrence of E(Pc) across such divergent species is unusual for both PcG proteins and for suppressors of position-effect variegation, and suggests that E(Pc) has an important role in the regulation of chromatin structure in eukaryotes.
果蝇中的多梳基因家族是同源异型开关基因调控因子,它们通过一种可能的染色质调控机制维持同源异型基因的抑制状态。果蝇的多梳增强子(E(Pc))基因是多梳基因家族中的一个特殊成员。大多数多梳基因(PcG)具有同源异型表型,是抑制同源异型基因座所必需的,但E(Pc)基因的突变并不表现出同源异型转变,对Abd - B基因的表达只有非常微弱的影响。然而,E(Pc)基因的突变是许多多梳基因家族基因突变的强增强子,也是位置效应斑驳的强抑制子,这表明E(Pc)在染色质形成或基因调控中可能比其他多梳基因家族基因具有更广泛的作用。E(Pc)基因通过转座子标签法克隆得到,编码一种新的含有2023个氨基酸的蛋白质,该蛋白质富含谷氨酰胺、丙氨酸和天冬酰胺区域。E(Pc)在果蝇胚胎发育过程中普遍表达。E(Pc)是一种染色质蛋白,在多线染色体上约100个位点结合,包括触角足复合体,但不包括双胸复合体,其中29%的结合位点与多梳蛋白结合位点相同。令人惊讶的是,在异染色质着丝粒中未检测到E(Pc)。这一结果表明,E(Pc)在异染色质形成中具有功能性而非结构性作用,这与多梳基因功能的异染色质模型相悖。利用同源克隆技术,我们鉴定出了E(Pc)的小鼠同源物,称为Epc1;一种酵母蛋白,我们命名为EPL1;以及来自秀丽隐杆线虫、小鼠和人类的其他EST序列。Epc1在其氨基末端与E(Pc)共享一个长的、高度保守的结构域,该结构域在酵母、秀丽隐杆线虫和人类中也保守。E(Pc)在如此不同的物种中出现,对于多梳基因蛋白和位置效应斑驳抑制子来说都是不寻常的,这表明E(Pc)在真核生物染色质结构的调控中具有重要作用。