A minisatellite "core" element constitutes a novel, chromatin-specific activator of mts1 gene transcription

被引:13
作者
Prokhortchouk, EB
Prokhortchouk, AV
Rouzov, AS
Kiselev, SL
Lukanidin, EM
Georgiev, GP
机构
[1] Inst Gene Biol, Lab Mol Canc Genet, Moscow 117334, Russia
[2] Danish Canc Soc, Div Canc Biol, DK-2100 Copenhagen, Denmark
基金
俄罗斯基础研究基金会;
关键词
minisatellite DNA; DNase I hypersensitive sites; transcription; chromatin; enhancer;
D O I
10.1006/jmbi.1998.1857
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of the mts1 gene is often associated with malignant transformation of tumor cells. Transcription of the gene is controlled by a number of positive and negative regulatory elements, all of them being localized in the first intron (+38 to +1215) of the mts1 gene. Through analysis of the distribution of DNase I hypersensitive sites in the first intron of the gene we revealed a structurally conserved region that consisted of a noncanonical NFkB binding site and a minisatellite "core" element. Deletion of the minisatellite core DNA in the context of the first intron had no effect on its regulatory capacity when assayed in transient transfections, while a fivefold decrease was observed in a pool of stably transfected cells. The minisatellite core sequence CTGGGCAGGCAG is involved in DNA-protein interactions in vivo, and is similar to a binding site for the previously identified minisatellite DNA sequence binding protein (Msbp1). The core DNA interacted in vitro with a protein that had an apparent molecular mass of 40 kDa. These data indicate that the minisatellite DNA represents the novel, chromatin-specific element in the mts1 complex enhancer. (C) 1998 Academic Press.
引用
收藏
页码:227 / 236
页数:10
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