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神经元限制性沉默因子对Pax4配对型同源结构域基因的调控

Regulation of Pax4 paired homeodomain gene by neuron-restrictive silencer factor.

作者信息

Kemp Daniel M, Lin Julia C, Habener Joel F

机构信息

Laboratory of Molecular Endocrinology, Massachusetts General Hospital, Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02114, USA.

出版信息

J Biol Chem. 2003 Sep 12;278(37):35057-62. doi: 10.1074/jbc.M305891200. Epub 2003 Jun 26.

Abstract

An elucidation of the key regulatory factors in pancreas development is critical for understanding the pathogenesis of diabetes mellitus. This study examined whether a specific regulatory mechanism that exists in neuronal development also plays a role in the pancreas. In non-neuronal cells, neuron-restrictive silencer factor (NSRF) actively represses gene transcription via a sequence-specific DNA motif known as the neuron-restrictive silencer element (NRSE). This DNA motif has been identified in many genes that are specific markers for cells of neuronal and neuroendocrine lineage. We identified several genes involved in pancreas development that also harbor NRSE-like motifs, including pdx-1, Beta2/NeuroD, and pax4. The paired homeodomain transcription factor Pax4 is implicated in the differentiation of the insulin-producing beta-cell lineage because disruption of the pax4 gene results in a severe deficiency of beta-cells and the manifestation of diabetes mellitus in mice. The NRSE-like motif identified in the upstream pax4 promoter is highly conserved throughout evolution, forms a DNA-protein complex with NRSF, and confers NRSF-dependent transcriptional repression in the context of a surrogate gene promoter. This cis-activating NRSE element also confers NRSF-dependent modulation in the context of the native pax4 gene promoter. Together with earlier reports, these new findings suggest an important functional role for NRSF in the expression of the pax4 gene and infer a role for NRSF in pancreatic islet development.

摘要

阐明胰腺发育中的关键调节因子对于理解糖尿病的发病机制至关重要。本研究探讨了神经元发育中存在的特定调节机制是否也在胰腺中发挥作用。在非神经元细胞中,神经元限制性沉默因子(NSRF)通过一种称为神经元限制性沉默元件(NRSE)的序列特异性DNA基序积极抑制基因转录。这种DNA基序已在许多作为神经元和神经内分泌谱系细胞特异性标志物的基因中被鉴定出来。我们鉴定了几个参与胰腺发育且也含有类NRSE基序的基因,包括pdx-1、Beta2/NeuroD和pax4。配对的同源结构域转录因子Pax4与产生胰岛素的β细胞谱系的分化有关,因为pax4基因的破坏会导致β细胞严重缺乏以及小鼠出现糖尿病症状。在pax4启动子上游鉴定出的类NRSE基序在整个进化过程中高度保守,与NSRF形成DNA-蛋白质复合物,并在替代基因启动子的背景下赋予NSRF依赖性转录抑制作用。这种顺式激活的NRSE元件在天然pax4基因启动子的背景下也赋予NSRF依赖性调节作用。与早期报告一起,这些新发现表明NSRF在pax4基因表达中具有重要的功能作用,并推断NSRF在胰岛发育中发挥作用。

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