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一个依赖多梳蛋白和GAGA因子的沉默子毗邻果蝇双胸复合体中的Fab-7边界。

A Polycomb and GAGA dependent silencer adjoins the Fab-7 boundary in the Drosophila bithorax complex.

作者信息

Hagstrom K, Muller M, Schedl P

机构信息

Department of Molecular Biology, Princeton University, New Jersey 08544, USA.

出版信息

Genetics. 1997 Aug;146(4):1365-80. doi: 10.1093/genetics/146.4.1365.

Abstract

The homeotic genes of the Drosophila bithorax complex are controlled by a large cis-regulatory region that ensures their segmentally restricted pattern of expression. A deletion that removes the Frontabdominal-7 cis-regulatory region (Fab-7') dominantly transforms parasegment 11 into parasegment 12. Previous studies suggested that removal of a domain boundary element on the proximal side of Fab-7' is responsible for this gain-of-function phenotype. In this article we demonstrate that the Fab-7' deletion also removes a silencer element, the iab-7 PRE, which maps to a different DNA segment and plays a different role in regulating parasegment-specific expression patterns of the Abd-B gene. The iab-7 PRE mediates pairing-sensitive silencing of mini-white, and can maintain the segmentally restricted expression pattern of a BXD, Ubx/lacZ reporter transgene. Both silencing activities depend upon Polycomb Group proteins. Pairing-sensitive silencing is relieved by removing the transvection protein Zeste, but is enhanced in a novel pairing-independent manner by the zeste' allele. The iab-7 PRE silencer is contained within a 0.8-kb fragment that spans a nuclease hypersensitive site, and silencing appears to depend on the chromatin remodeling protein, the GAGA factor.

摘要

果蝇双胸复合体的同源异型基因受一个大的顺式调控区域控制,该区域确保它们在各节段中受到限制的表达模式。一个缺失了腹前7顺式调控区域(Fab-7')的缺失突变会将第11副节显性转化为第12副节。先前的研究表明,去除Fab-7'近端的一个结构域边界元件是导致这种功能获得性表型的原因。在本文中,我们证明Fab-7'缺失还去除了一个沉默元件,即iab-7 PRE,它定位于不同的DNA片段,并且在调节Abd-B基因的副节特异性表达模式中发挥不同作用。iab-7 PRE介导对mini-white的配对敏感沉默,并能维持BXD、Ubx/lacZ报告基因转基因的节段特异性表达模式。这两种沉默活性都依赖于多梳蛋白家族。通过去除转座蛋白Zeste可以解除配对敏感沉默,但zeste'等位基因会以一种新的不依赖配对的方式增强这种沉默。iab-7 PRE沉默子包含在一个跨越核酸酶超敏感位点的0.8 kb片段内,沉默似乎依赖于染色质重塑蛋白GAGA因子。

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