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通过核心启动子和基础转录机制调控基因表达。

Regulation of gene expression via the core promoter and the basal transcriptional machinery.

机构信息

Section of Molecular Biology, 0347, University of California, San Diego, La Jolla, CA 92093-0347, USA.

出版信息

Dev Biol. 2010 Mar 15;339(2):225-9. doi: 10.1016/j.ydbio.2009.08.009. Epub 2009 Aug 13.

DOI:10.1016/j.ydbio.2009.08.009
PMID:19682982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2830304/
Abstract

The RNA polymerase II core promoter is a structurally and functionally diverse transcriptional regulatory element. There are two main strategies for transcription initiation - focused and dispersed initiation. In focused initiation, transcription starts from a single nucleotide or within a cluster of several nucleotides, whereas in dispersed initiation, there are several weak transcription start sites over a broad region of about 50 to 100 nucleotides. Focused initiation is the predominant means of transcription in simpler organisms, whereas dispersed initiation is observed in approximately two-thirds of vertebrate genes. Regulated genes tend to have focused promoters, and constitutive genes typically have dispersed promoters. Hence, in vertebrates, focused promoters are used in a small but biologically important fraction of genes. The properties of focused core promoters are dependent upon the presence or absence of sequence motifs such as the TATA box and DPE. For example, Caudal, a key regulator of the homeotic gene network, preferentially activates transcription from DPE- versus TATA-dependent promoters. The basal transcription factors, which act in conjunction with the core promoter, are another important component in the regulation of gene expression. For instance, upon differentiation of myoblasts to myotubes, the cells undergo a switch from a TFIID-based transcription system to a TRF3-TAF3-based system. These findings suggest that the core promoter and basal transcription factors are important yet mostly unexplored components in the regulation of gene expression.

摘要

RNA 聚合酶 II 核心启动子是一种结构和功能多样化的转录调控元件。有两种主要的转录起始策略——集中起始和分散起始。在集中起始中,转录从单个核苷酸或几个核苷酸的簇开始,而在分散起始中,在大约 50 到 100 个核苷酸的广泛区域中有几个较弱的转录起始位点。集中起始是简单生物中主要的转录方式,而分散起始则存在于大约三分之二的脊椎动物基因中。受调控的基因往往具有集中的启动子,而组成型基因通常具有分散的启动子。因此,在脊椎动物中,集中启动子被用于一小部分但在生物学上重要的基因中。集中核心启动子的特性取决于序列基序的存在或缺失,例如 TATA 盒和 DPE。例如,Caudal 是同源基因网络的关键调节剂,它优先激活 DPE 而非 TATA 依赖性启动子的转录。与核心启动子协同作用的基础转录因子是基因表达调控中的另一个重要组成部分。例如,在成肌细胞分化为肌管时,细胞经历了从基于 TFIID 的转录系统到基于 TRF3-TAF3 的系统的转变。这些发现表明,核心启动子和基础转录因子是基因表达调控中重要但大多未被探索的组成部分。

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