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CCAAT/增强子结合蛋白β(C/EBP-β),大鼠过氧化氢酶基因中无TATA盒启动子的关键调节因子。

CCAAT/enhancer binding protein-beta (C/EBP-beta), a pivotal regulator of the TATA-less promoter in the rat catalase gene.

作者信息

Taniguchi Makoto, Hashimoto Mayumi, Hori Naohiro, Sato Kenzo

机构信息

Division of Molecular Biology, Department of Molecular and Cellular Biology, School of Life Sciences, Faculty of Medicine, Tottori University, Yonago, Japan.

出版信息

FEBS Lett. 2005 Oct 24;579(25):5785-90. doi: 10.1016/j.febslet.2005.09.068. Epub 2005 Oct 6.

Abstract

The rat catalase gene carries a TATA-less promoter and its transcriptional mechanism is interesting because of downregulation in liver injury. We characterized the core element in the promoter and found that C/EBP-beta binding downstream of the transcription initiation site plays a crucial role for transcription. The multiple complexes binding to the promoter were composed of homodimers and heterodimers of C/EBP-beta isoforms. Transduction of the C/EBP-beta gene showed complete reconstitution of multiple binding complexes in HeLa cells, similar to normal liver. Furthermore, C/EBP-beta was observed to bind to the endogenous catalase promoter. These data suggest that multiple complex formation of C/EBP-beta regulates transcription in the TATA-less catalase promoter.

摘要

大鼠过氧化氢酶基因携带一个无TATA盒的启动子,其转录机制因在肝损伤中下调而备受关注。我们对该启动子中的核心元件进行了表征,发现转录起始位点下游的C/EBP-β结合对转录起着关键作用。与启动子结合的多个复合物由C/EBP-β亚型的同二聚体和异二聚体组成。C/EBP-β基因的转导显示,在HeLa细胞中多个结合复合物完全重建,类似于正常肝脏。此外,观察到C/EBP-β与内源性过氧化氢酶启动子结合。这些数据表明,C/EBP-β的多个复合物形成调节无TATA盒的过氧化氢酶启动子中的转录。

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