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细胞色素c氧化酶亚基VIIa肝脏异构体。牛基因启动子元件的特性与鉴定。

Cytochrome c oxidase subunit VIIa liver isoform. Characterization and identification of promoter elements in the bovine gene.

作者信息

Seelan R S, Gopalakrishnan L, Scarpulla R C, Grossman L I

机构信息

Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, USA.

出版信息

J Biol Chem. 1996 Jan 26;271(4):2112-20. doi: 10.1074/jbc.271.4.2112.

Abstract

Cytochrome c oxidase subunit VIIa is specified by two nuclear genes, one (COX7AH) producing a heart/muscle-specific isoform and the other (COX7AL) a form expressed in all tissues. We have isolated both genes to examine their transcriptional regulation. Here, we characterize the core promoter of COX7AL and show that a 92-base pair region flanking the 5'-end promotes most of the activity of this gene. The 92-bp basal promoter contains sites for the nuclear respiratory factors NRF-1 and NRF-2, which have been shown to contribute to the transcription of a number of nuclear genes involved in mitochondrial respiratory activity, and also at least four Sp1 motifs. We show that both the NRF-1 and NRF-2 binding sites are functional in COX7AL and present evidence suggesting that interaction between the NRF-1 site and an upstream element contributes to expression.

摘要

细胞色素c氧化酶亚基VIIa由两个核基因指定,一个(COX7AH)产生心脏/肌肉特异性同工型,另一个(COX7AL)产生在所有组织中表达的一种形式。我们分离了这两个基因以研究它们的转录调控。在这里,我们对COX7AL的核心启动子进行了表征,并表明位于5'端侧翼的一个92个碱基对的区域促进了该基因的大部分活性。这个92碱基对的基础启动子包含核呼吸因子NRF-1和NRF-2的位点,这些位点已被证明有助于许多参与线粒体呼吸活动的核基因的转录,并且还至少包含四个Sp1基序。我们表明NRF-1和NRF-2结合位点在COX7AL中都具有功能,并提供证据表明NRF-1位点与上游元件之间的相互作用有助于表达。

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