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A10平滑肌细胞中的端激酶表达需要血清反应因子。

Telokin expression in A10 smooth muscle cells requires serum response factor.

作者信息

Herring B P, Smith A F

机构信息

Department of Physiology and Biophysics, Indiana University School of Medicine, Indianapolis 46202, USA.

出版信息

Am J Physiol. 1997 Apr;272(4 Pt 1):C1394-404. doi: 10.1152/ajpcell.1997.272.4.C1394.

Abstract

Telokin transcription is initiated from a smooth muscle-specific promoter located in an intron of the smooth muscle myosin light chain kinase gene. We have previously identified a 310-base pair fragment of the promoter that mediates A10 smooth muscle cell-specific expression of telokin. In the current study, telokin-luciferase reporter gene assays in A10 cells and REF52 nonmuscle cells revealed that the promoter region between -81 and +80 contains the regulatory elements required to mediate the in vitro cell specificity of the promoter. Several positive-acting elements, including an E box, myocyte enhancer factor 2 (MEF2)-TATA box, and CArG-serum response element, were identified within this region. Telokin transcription in A10 smooth muscle cells requires all three transcription initiation sites and an AT-rich sequence between -71 and -62 that includes a TATA box. MEF2 interacts with the AT-rich region with low affinity; however, MEF2 binding is not required for transcriptional activity in A10 cells. Binding of serum response factor (SRF) to a CArG element proximal to the TATA sequence is also critical for high levels of transcription in A10 cells. Together these data suggest that an AT-rich motif, acting in concert with SRF and an unusual transcription initiation mechanism, is required for the cell-specific expression of the telokin promoter in A10 smooth muscle cells.

摘要

端激酶转录起始于位于平滑肌肌球蛋白轻链激酶基因内含子中的平滑肌特异性启动子。我们之前已鉴定出该启动子的一个310碱基对片段,它介导端激酶在A10平滑肌细胞中的特异性表达。在当前研究中,对A10细胞和REF52非肌肉细胞进行的端激酶-荧光素酶报告基因检测显示,-81至+80之间的启动子区域包含介导该启动子体外细胞特异性所需的调控元件。在该区域内鉴定出了几个正向作用元件,包括一个E盒、肌细胞增强因子2(MEF2)-TATA盒和CArG-血清反应元件。A10平滑肌细胞中的端激酶转录需要所有三个转录起始位点以及-71至-62之间的富含AT的序列,该序列包含一个TATA盒。MEF2以低亲和力与富含AT的区域相互作用;然而,MEF2结合对于A10细胞中的转录活性并非必需。血清反应因子(SRF)与TATA序列近端的CArG元件结合对于A10细胞中的高水平转录也至关重要。这些数据共同表明,在A10平滑肌细胞中,端激酶启动子的细胞特异性表达需要一个富含AT的基序与SRF协同作用以及一种不同寻常的转录起始机制。

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