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启动子元件的功能是决定 BX-C 增强子的活性状态。

Initiator elements function to determine the activity state of BX-C enhancers.

机构信息

National Centre of Competence in Research (NCCR) Frontiers in Genetics and Department of Zoology and Animal Biology, University of Geneva, Geneva, Switzerland.

出版信息

PLoS Genet. 2010 Dec 23;6(12):e1001260. doi: 10.1371/journal.pgen.1001260.

Abstract

A >300 kb cis-regulatory region is required for the proper expression of the three bithorax complex (BX-C) homeotic genes. Based on genetic and transgenic analysis, a model has been proposed in which the numerous BX-C cis-regulatory elements are spatially restricted through the activation or repression of parasegment-specific chromatin domains. Particular early embryonic enhancers, called initiators, have been proposed to control this complex process. Here, in order to better understand the process of domain activation, we have undertaken a systematic in situ dissection of the iab-6 cis-regulatory domain using a new method, called InSIRT. Using this method, we create and genetically characterize mutations affecting iab-6 function, including mutations specifically modifying the iab-6 initiator. Through our mutagenesis of the iab-6 initiator, we provide strong evidence that initiators function not to directly control homeotic gene expression but rather as domain control centers to determine the activity state of the enhancers and silencers within a cis-regulatory domain.

摘要

一个超过 300kb 的顺式调控区对于正确表达三个同源异型盒复合体(BX-C)的同源基因是必需的。基于遗传和转基因分析,提出了一个模型,其中众多 BX-C 顺式调控元件通过激活或抑制分段特异性染色质域而在空间上受到限制。已经提出了特定的早期胚胎增强子,称为起始子,来控制这个复杂的过程。在这里,为了更好地理解域激活的过程,我们使用一种称为 InSIRT 的新方法对 iab-6 顺式调控域进行了系统的原位剖析。使用这种方法,我们创建并遗传表征了影响 iab-6 功能的突变,包括专门修饰 iab-6 起始子的突变。通过对 iab-6 起始子的诱变,我们提供了强有力的证据表明,起始子的功能不是直接控制同源基因的表达,而是作为域控制中心来确定顺式调控域内增强子和沉默子的活性状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d21f/3009686/ba4cd9814985/pgen.1001260.g001.jpg

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