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新型碳酸酐酶VI的CHOP依赖性应激诱导表达。

CHOP-Dependent stress-inducible expression of a novel form of carbonic anhydrase VI.

作者信息

Sok J, Wang X Z, Batchvarova N, Kuroda M, Harding H, Ron D

机构信息

Skirball Institute of Biomolecular Medicine, Departments of Medicine and Cell Biology, and Kaplan Cancer Center, New York University Medical Center, New York, New York 10016, USA.

出版信息

Mol Cell Biol. 1999 Jan;19(1):495-504. doi: 10.1128/MCB.19.1.495.

Abstract

CHOP (also called GADD153) is a stress-inducible nuclear protein that dimerizes with members of the C/EBP family of transcription factors and was initially identified as an inhibitor of C/EBP binding to classic C/EBP target genes. Subsequent experiments suggested a role for CHOP-C/EBP heterodimers in positively regulating gene expression; however, direct evidence that this is the case has so far not been uncovered. Here we describe the identification of a positively regulated direct CHOP-C/EBP target gene, that encoding murine carbonic anhydrase VI (CA-VI). The stress-inducible form of the gene is expressed from an internal promoter and encodes a novel intracellular form of what is normally a secreted protein. Stress-induced expression of CA-VI is both CHOP and C/EBPbeta dependent in that it does not occur in cells deficient in either gene. A CHOP-responsive element was mapped to the inducible CA-VI promoter, and in vitro footprinting revealed binding of CHOP-C/EBP heterodimers to that site. Rescue of CA-VI expression in c/ebpbeta-/- cells by exogenous C/EBPbeta and a shorter, normally inhibitory isoform of the protein known as LIP suggests that the role of the C/EBP partner is limited to targeting the CHOP-containing heterodimer to the response element and points to a preeminent role for CHOP in CA-VI induction during stress.

摘要

CHOP(也称为GADD153)是一种应激诱导型核蛋白,它与转录因子C/EBP家族的成员形成二聚体,最初被鉴定为C/EBP与经典C/EBP靶基因结合的抑制剂。随后的实验表明CHOP-C/EBP异二聚体在正向调节基因表达中起作用;然而,迄今为止尚未发现直接证据证明情况确实如此。在这里,我们描述了一个正向调节的直接CHOP-C/EBP靶基因的鉴定,该基因编码小鼠碳酸酐酶VI(CA-VI)。该基因的应激诱导形式由一个内部启动子表达,并编码一种通常为分泌蛋白的新型细胞内形式。CA-VI的应激诱导表达依赖于CHOP和C/EBPβ,因为在这两个基因缺陷的细胞中不会发生这种情况。一个CHOP反应元件被定位到可诱导的CA-VI启动子上,体外足迹实验揭示了CHOP-C/EBP异二聚体与该位点的结合。通过外源性C/EBPβ和该蛋白的一种较短的、通常具有抑制作用的同工型LIP来拯救c/ebpβ-/-细胞中CA-VI的表达,这表明C/EBP伙伴的作用仅限于将含CHOP的异二聚体靶向反应元件,并指出CHOP在应激期间CA-VI诱导中起主要作用。

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