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大鼠MRF4基因的远端调控区域。

Distal regulatory regions of the rat MRF4 gene.

作者信息

Kerkvliet C M, Hinterberger T J

机构信息

Biomedical Program and Department of Biological Sciences, University of Alaska Anchorage, 99508, USA.

出版信息

Biochem Biophys Res Commun. 1997 Aug 8;237(1):170-6. doi: 10.1006/bbrc.1997.6980.

Abstract

MRF4 is a muscle-specific transcription factor that is expressed both in embryonic somites and later in fetal and adult muscle fibers. Cis-regulatory elements of the MRF4 gene responsible for its complex expression pattern have not yet been identified, although previous studies of the rat MRF4 gene have demonstrated the presence of enhancer activity located several kilobases 5' to the transcription start site. Using cell transfection assays in vitro, we have now localized one of the regulatory regions of MRF4 to a 590-base-pair sequence between 4 and 5 kilobases upstream from the start site. This sequence region functioned as an enhancer in combination either with the MRF4 promoter or with the viral thymidine kinase (tk) promoter. Deletion analysis of MRF4 indicated the existence of another regulatory region, closer to the promoter, which functioned as an enhancer in combination with the MRF4 promoter but not with the tk promoter.

摘要

MRF4是一种肌肉特异性转录因子,在胚胎体节以及随后的胎儿和成年肌纤维中均有表达。尽管先前对大鼠MRF4基因的研究已证明在转录起始位点上游数千碱基处存在增强子活性,但负责其复杂表达模式的MRF4基因顺式调控元件尚未确定。通过体外细胞转染试验,我们现已将MRF4的一个调控区域定位到起始位点上游4至5千碱基之间的一段590个碱基对的序列。该序列区域与MRF4启动子或病毒胸苷激酶(tk)启动子结合时可发挥增强子的作用。对MRF4的缺失分析表明存在另一个更靠近启动子的调控区域,该区域与MRF4启动子结合时可发挥增强子的作用,但与tk启动子结合时则不然。

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