TRANSCRIPTIONAL REGULATION OF THE APOLIPOPROTEIN-B-100 GENE - IDENTIFICATION OF CIS-ACTING ELEMENTS IN THE FIRST NONTRANSLATED EXON OF THE HUMAN APOLIPOPROTEIN-B-100 GENE

被引:12
作者
CHUANG, SS
ZHUANG, HM
REISHER, SR
FEINSTEIN, SI
DAS, HK
机构
[1] UNIV N TEXAS,CTR HLTH SCI,DEPT PHARMACOL,FT WORTH,TX 76107
[2] UNIV TENNESSEE,CTR HLTH SCI,DEPT MICROBIOL IMMUNOL,MEMPHIS,TN 38163
[3] UNIV PENN,SCH MED,INST ENVIRONM MED,PHILADELPHIA,PA 19104
[4] UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
关键词
D O I
10.1006/bbrc.1995.2478
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
Apolipoprotein B-100, produced primarily in the human liver, is the sole protein component of low-density lipoprotein and serves as a ligand for the LDL receptor. Two cis-acting positive elements between -128 and -70 control hepatic cell-specific expression of the human apoB gene (H. K. Das, T. Leff, and J. L. Breslow, J. Biol. Chem. 263: 11452-11458, 1988). In this study, two apoB cis-acting elements (+20 to +40; +43 to +53) have been identified using DNase I footprint analysis. Through in vitro mutagenesis and transient transfection experiments in Hep G2 and HeLa cells, the element (+20 to +40) was observed to have a negative effect on transcription of the apoB gene. The element (+43 to +53) was found to have a strong positive effect on apoB gene transcription in Hep G2 cells and mild positive effect in HeLa cells. Therefore these two cis-acting elements mediate hepatic-cell specific expression of the apolipoprotein gene by interacting with trans-acting protein factors. (C) 1995 Academic Press. Inc.
引用
收藏
页码:394 / 404
页数:11
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