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在动脉平滑肌细胞中,结蛋白基因转录的调控需要一个重叠的CArG/八聚体元件。

An overlapping CArG/octamer element is required for regulation of desmin gene transcription in arterial smooth muscle cells.

作者信息

Mericskay M, Parlakian A, Porteu A, Dandré F, Bonnet J, Paulin D, Li Z

机构信息

Laboratoire de Biologie Moléculaire de la Différenciation, Université Denis Diderot Paris 7, 2, place Jussieu, Paris, 75005, France.

出版信息

Dev Biol. 2000 Oct 15;226(2):192-208. doi: 10.1006/dbio.2000.9865.

Abstract

The desmin gene encodes an intermediate filament protein that is present in skeletal, cardiac, and smooth muscle cells. This study shows that the 4-kb upstream region of the murine desmin promoter directs expression of a lacZ reporter gene throughout the heart from E7.5 and in skeletal muscle and vascular smooth muscle cells from E9. 5. The distal fragment (-4005/-2495) is active in arterial smooth muscle cells but not in venous smooth muscle cells or in the heart in vivo. It contains a CArG/octamer overlapping element (designated CArG4) that can bind the serum response factor (SRF) and an Oct-like factor. The desmin distal fragment can replace a SM22alpha regulatory region (-445/-126) that contains two CArG boxes, to cis-activate a minimal (-125/+65) SM22alpha promoter fragment in arterial smooth muscle cells of transgenic embryos. lacZ expression was abolished when mutations were introduced into the desmin CArG4 element that abolished the binding of SRF and/or Oct-like factor. These data suggest that a new type of combined CArG/octamer element plays a prominent role in the regulation of the desmin gene in arterial smooth muscle cells, and SRF and Oct-like factor could cooperate to drive specific expression in these cells.

摘要

结蛋白基因编码一种中间丝蛋白,该蛋白存在于骨骼肌、心肌和平滑肌细胞中。本研究表明,小鼠结蛋白启动子的4 kb上游区域在胚胎第7.5天开始指导lacZ报告基因在整个心脏中表达,并在胚胎第9.5天开始在骨骼肌和血管平滑肌细胞中表达。远端片段(-4005/-2495)在体内的动脉平滑肌细胞中有活性,但在静脉平滑肌细胞或心脏中无活性。它包含一个可结合血清反应因子(SRF)和一个Oct样因子的CArG/八聚体重叠元件(称为CArG4)。结蛋白远端片段可以取代含有两个CArG框的SM22α调控区域(-445/-126),以顺式激活转基因胚胎动脉平滑肌细胞中的最小(-125/+65)SM22α启动子片段。当将突变引入结蛋白CArG4元件中,从而消除SRF和/或Oct样因子的结合时,lacZ表达被消除。这些数据表明,一种新型的组合CArG/八聚体元件在动脉平滑肌细胞中结蛋白基因的调控中起重要作用,并且SRF和Oct样因子可能协同驱动这些细胞中的特异性表达。

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