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MHC I类基因表达受到原癌基因c-jun的负调控。

MHC class I gene expression is negatively regulated by the proto-oncogene, c-jun.

作者信息

Howcroft T K, Richardson J C, Singer D S

机构信息

Experimental Immunology Branch, NCI, NIH, Bethesda, MD 20892.

出版信息

EMBO J. 1993 Aug;12(8):3163-9. doi: 10.1002/j.1460-2075.1993.tb05985.x.

Abstract

The trans-acting factor AP-1 is a heterodimeric complex composed of c-Jun and c-Fos family proteins which bind and regulate genes containing a TPA responsive enhancer element. Although AP-1 binding sites have been identified within the regulatory region of major histocompatibility complex (MHC) class I genes in vitro, the role of AP-1 in regulating MHC class I transcription in vivo has not been investigated previously. The present study demonstrates that expression of c-Jun results in decreased MHC class I promoter activity as determined in cotransfection assays of an MHC class I reporter construct with a c-Jun expression construct. The c-Jun responsive element is located between bp -440 and -431 upstream of initiation of transcription as determined both functionally and by direct binding of purified c-Jun. Furthermore, over-expression of c-Jun reduced the steady state levels of endogenous MHC class I RNA in murine L cells by approximately 10-fold. These data indicate that c-Jun/AP-1 acts as a negative trans-acting factor that down-regulates MHC class I gene expression.

摘要

反式作用因子AP-1是一种由c-Jun和c-Fos家族蛋白组成的异二聚体复合物,它能结合并调控含有佛波酯反应增强子元件的基因。虽然在体外已经在主要组织相容性复合体(MHC)I类基因的调控区域内鉴定出了AP-1结合位点,但此前尚未研究过AP-1在体内调控MHC I类转录中的作用。本研究表明,如在MHC I类报告基因构建体与c-Jun表达构建体的共转染实验中所确定的那样,c-Jun的表达导致MHC I类启动子活性降低。通过功能测定以及纯化的c-Jun的直接结合确定,c-Jun反应元件位于转录起始上游-440至-431碱基对之间。此外,c-Jun的过表达使小鼠L细胞中内源性MHC I类RNA的稳态水平降低了约10倍。这些数据表明,c-Jun/AP-1作为一种负反式作用因子下调MHC I类基因的表达。

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