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pdx-1基因表达的调控。

Regulation of pdx-1 gene expression.

作者信息

Melloul Danielle, Marshak Sonya, Cerasi Erol

机构信息

Department of Endocrinology and Metabolism, Hadassah University Hospital, Jerusalem, Israel.

出版信息

Diabetes. 2002 Dec;51 Suppl 3:S320-5. doi: 10.2337/diabetes.51.2007.s320.

Abstract

The homeodomain-containing transcription factor pancreatic duodenal homeobox 1 (PDX-1) plays a key role in pancreas development and in beta-cell function. Upstream sequences of the gene up to about -6 kb show islet-specific activity in transgenic mice. Attempts to identify functional regulatory elements involved in the controlled expression of the pdx-1 gene led to the identification of distinct distal beta-cell-specific enhancers in human and rat genes. Three additional sequences, conserved between the mouse and the human 5'-flanking regions, two of which are also found in the chicken gene, conferred beta-cell-specific expression on a reporter gene, albeit to different extents. A number of transcription factors binding to and modulating the transcriptional activity of the regulatory elements were identified, such as hepatocyte nuclear factor (HNF)-3beta, HNF-1alpha, SP1/3, and, interestingly, PDX-1 itself. A fourth conserved region was localized to the proximal promoter around an E-box motif and was found to bind members of the upstream stimulatory factor (USF) family of transcription factors. We postulate that disruption of pdx-1 cis-acting regulatory sequences and/or mutations or functional impairment of transcription factors controlling the expression of the gene can lead to diabetes.

摘要

含同源结构域的转录因子胰腺十二指肠同源盒1(PDX-1)在胰腺发育和β细胞功能中起关键作用。该基因上游约-6 kb的序列在转基因小鼠中表现出胰岛特异性活性。为了鉴定参与pdx-1基因可控表达的功能调控元件,人们在人类和大鼠基因中鉴定出了不同的远端β细胞特异性增强子。在小鼠和人类5'侧翼区域之间保守的另外三个序列,其中两个在鸡基因中也有发现,它们赋予了报告基因β细胞特异性表达,尽管程度不同。人们鉴定出了许多与调控元件结合并调节其转录活性的转录因子,如肝细胞核因子(HNF)-3β、HNF-1α、SP1/3,有趣的是,还有PDX-1本身。第四个保守区域定位于E-box基序周围的近端启动子,发现它能结合上游刺激因子(USF)转录因子家族的成员。我们推测,pdx-1顺式作用调控序列的破坏和/或控制该基因表达的转录因子的突变或功能受损可能导致糖尿病。

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