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Analysis of the c-myc P2 promoter.

作者信息

Moberg K H, Tyndall W A, Pyrc J, Hall D J

机构信息

Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.

出版信息

J Cell Physiol. 1991 Jul;148(1):75-84. doi: 10.1002/jcp.1041480110.

DOI:10.1002/jcp.1041480110
PMID:1860897
Abstract

The cis-acting elements governing transcription from the murine c-myc P2 promoter have not been well defined. To gain a better understanding of the nature of the protein-DNA interactions that take place on the P2 promoter, protein binding assays were performed. The ME1a2 and E2F factors appear to be the predominant proteins bound to a region spanning positions -140 to -24 relative to the P2 transcription start site. By a number of criteria, these factors appear to be distinct. When c-myc promoter sequences were coupled to the chloramphenicol acetyltransferase gene (CAT) and transiently transfected into tissue culture cells it was found that optimal transcription from P2 was heavily dependent on the ME1a2 element.

摘要

相似文献

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The Myc negative autoregulation mechanism requires Myc-Max association and involves the c-myc P2 minimal promoter.Myc负向自调控机制需要Myc与Max结合,并涉及c-myc P2最小启动子。
Mol Cell Biol. 1997 Jan;17(1):100-14. doi: 10.1128/MCB.17.1.100.
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Repeated CT elements bound by zinc finger proteins control the absolute and relative activities of the two principal human c-myc promoters.
与锌指蛋白结合的重复CT元件控制着人类两个主要c-myc启动子的绝对活性和相对活性。
Mol Cell Biol. 1993 Sep;13(9):5710-24. doi: 10.1128/mcb.13.9.5710-5724.1993.