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pdx-1基因保守的转录调控结构域。

Conserved transcriptional regulatory domains of the pdx-1 gene.

作者信息

Gerrish Kevin, Van Velkinburgh Jennifer C, Stein Roland

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, 723 Light Hall, Nashville, Tennessee 37215, USA.

出版信息

Mol Endocrinol. 2004 Mar;18(3):533-48. doi: 10.1210/me.2003-0371. Epub 2003 Dec 30.

DOI:10.1210/me.2003-0371
PMID:14701942
Abstract

The pancreas and duodenum homeobox protein 1 (PDX-1) homeodomain-containing transcription factor affects both pancreatic endocrine cell development and adult islet beta-cell function. Cell-type-specific expression is controlled by sequences 5' flanking the pdx-1 gene transcription start site. One principal control region is located roughly between -2800 and -1600 bp and spans three conserved, distinct, and functionally important subdomains, termed areas I, II, and III. In this study, we found that an upstream control region in the rat pdx-1 gene located between -6200 and -5670 bp is also present in the mouse, chicken, and human genes. This region is capable of independently directing pancreatic beta-cell-selective reporter gene expression and potentiating area I/II-driven activity. This newly recognized conserved subdomain has been termed area IV. The islet-enriched forkhead box A2 (FoxA2), NK2 homeobox 2.2 (Nkx2.2), and pancreas and duodenum homeobox protein 1 (PDX-1) transcription factors have been shown to activate area IV-driven reporter gene expression as well as bind to this region of the endogenous gene in beta-cells. Analysis of the histone H3 and H4 acetylation level also indicated that areas I-IV are within transcriptionally active chromatin in beta-cells. Our data suggests that pdx-1 transcription is also regulated by factors acting upon conserved area IV sequences.

摘要

胰腺十二指肠同源盒蛋白1(PDX-1)含同源结构域的转录因子影响胰腺内分泌细胞发育和成年胰岛β细胞功能。细胞类型特异性表达由pdx-1基因转录起始位点侧翼的5'序列控制。一个主要控制区域大致位于-2800至-1600 bp之间,跨越三个保守、独特且功能重要的亚结构域,称为区域I、II和III。在本研究中,我们发现大鼠pdx-1基因中位于-6200至-5670 bp之间的上游控制区域在小鼠、鸡和人类基因中也存在。该区域能够独立指导胰腺β细胞选择性报告基因表达并增强区域I/II驱动的活性。这个新识别出的保守亚结构域被称为区域IV。富含胰岛的叉头框A2(FoxA2)、NK2同源盒2.2(Nkx2.2)和胰腺十二指肠同源盒蛋白1(PDX-1)转录因子已被证明可激活区域IV驱动的报告基因表达,并与β细胞内源性基因的该区域结合。组蛋白H3和H4乙酰化水平分析也表明,区域I-IV位于β细胞中具有转录活性的染色质内。我们的数据表明,pdx-1转录也受作用于保守区域IV序列的因子调控。

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