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c-Myc诱导鸟氨酸脱羧酶的表达和活性。

c-Myc induces the expression and activity of ornithine decarboxylase.

作者信息

Wagner A J, Meyers C, Laimins L A, Hay N

机构信息

Department of Biochemistry and Molecular Biology, University of Chicago, Illinois 60637.

出版信息

Cell Growth Differ. 1993 Nov;4(11):879-83.

PMID:8297793
Abstract

The role of the product of the c-myc protooncogene in the regulation of cellular proliferation and differentiation is well established. Recent reports that c-Myc can serve as a sequence-specific transcriptional activator have begun to elucidate the mechanism by which c-Myc exerts such a profound effect on the mitotic status of a cell. To identify a potential target gene for Myc-mediated trans-activation, we examined the regulation of the ornithine decarboxylase (ODC) gene by c-Myc. ODC is the first and rate-limiting enzyme involved in the synthesis of the polyamines and has been shown to be required for entry into and progression through the cell cycle. Using a conditionally active c-Myc-estrogen receptor chimeric protein, we found estrogen-dependent activation of ODC expression and enzymatic activity. The induction of ODC mRNA expression was not dependent upon de novo protein synthesis. These data suggest that one downstream pathway for Myc-directed cell cycle control is the induction of ODC expression.

摘要

c-myc原癌基因产物在细胞增殖和分化调控中的作用已得到充分证实。最近有报道称c-Myc可作为序列特异性转录激活因子,这已开始阐明c-Myc对细胞有丝分裂状态产生如此深远影响的机制。为了确定Myc介导的反式激活的潜在靶基因,我们研究了c-Myc对鸟氨酸脱羧酶(ODC)基因的调控。ODC是多胺合成中首个且起限速作用的酶,并且已证明它是进入细胞周期和在细胞周期中进展所必需的。使用条件性激活的c-Myc-雌激素受体嵌合蛋白,我们发现ODC表达和酶活性呈雌激素依赖性激活。ODC mRNA表达的诱导不依赖于从头合成蛋白质。这些数据表明,Myc指导的细胞周期控制的一个下游途径是ODC表达的诱导。

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