EVOLUTIONARY DUPLICATION OF A HEPATIC CONTROL REGION IN THE HUMAN APOLIPOPROTEIN-E GENE LOCUS - IDENTIFICATION OF A 2ND REGION THAT CONFERS HIGH-LEVEL AND LIVER-SPECIFIC EXPRESSION OF THE HUMAN APOLIPOPROTEIN-E GENE IN TRANSGENIC MICE

被引:53
作者
ALLAN, CM
WALKER, D
TAYLOR, JM
机构
[1] UNIV CALIF SAN FRANCISCO,CARDIOVASC RES INST,SAN FRANCISCO,CA 94141
[2] UNIV CALIF SAN FRANCISCO,DEPT PHYSIOL,SAN FRANCISCO,CA 94141
关键词
D O I
10.1074/jbc.270.44.26278
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We have identified a second hepatic control region (HCR-2) in the human apolipoprotein (ape) E gene locus that confers liver expression of the human apoE gene in transgenic mice. This HCR-2 sequence is located 27 kilobases downstream of the apoE gene and 10 kilobases downstream of the previously described liver-specific enhancer (HCR-1), Nucleotide sequence analysis of the HCR-2 region revealed a sequence that shares 85% identity to the functional 319-base pair domain of HCR-1. To test its activity, transgenic mice were prepared with a fusion construct containing a human apoE gene fragment, which is not normally expressed in the liver, ligated to a 632-base pair region containing the HCR-2 sequence. This construct resulted in high levels of liver-specific apoE transgene expression, indicating that HCR-2 can function as a hepatic enhancer and has an activity similar to that of HCR-1. Hence, these findings suggest that there are at least two hepatic control regions, HCR-1 and HCR-2, capable of controlling the liver expression of this human apolipoprotein gene locus.
引用
收藏
页码:26278 / 26281
页数:4
相关论文
共 29 条
[1]
IDENTIFICATION AND CHARACTERIZATION OF A NEW HUMAN GENE (APOC4) IN THE APOLIPOPROTEIN-E, C-I, AND C-II GENE LOCUS [J].
ALLAN, CM ;
WALKER, D ;
SEGREST, JP ;
TAYLOR, JM .
GENOMICS, 1995, 28 (02) :291-300
[2]
AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
[3]
THE LDL RECEPTOR RELATED PROTEIN, LRP, IS AN APOLIPOPROTEIN-E-BINDING PROTEIN [J].
BEISIEGEL, U ;
WEBER, W ;
IHRKE, G ;
HERZ, J ;
STANLEY, KK .
NATURE, 1989, 341 (6238) :162-164
[4]
HYPERTRIGLYCERIDEMIA ASSOCIATED WITH DEFICIENCY OF APOLIPOPROTEIN-C-II [J].
BRECKENRIDGE, WC ;
LITTLE, JA ;
STEINER, G ;
CHOW, A ;
POAPST, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (23) :1265-1273
[5]
A RECEPTOR-MEDIATED PATHWAY FOR CHOLESTEROL HOMEOSTASIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
SCIENCE, 1986, 232 (4746) :34-47
[6]
APOLIPOPROTEIN-E MESSENGER-RNA IS ABUNDANT IN THE BRAIN AND ADRENALS, AS WELL AS IN THE LIVER, AND IS PRESENT IN OTHER PERIPHERAL-TISSUES OF RATS AND MARMOSETS [J].
ELSHOURBAGY, NA ;
LIAO, WS ;
MAHLEY, RW ;
TAYLOR, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (01) :203-207
[7]
TYPE-III HYPERLIPOPROTEINEMIC PHENOTYPE IN TRANSGENIC MICE EXPRESSING DYSFUNCTIONAL APOLIPOPROTEIN-E [J].
FAZIO, S ;
LEE, YL ;
JI, ZS ;
RALL, SC .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) :1497-1503
[8]
GILMAN M, 1993, CURRENT PROTOCOLS MO, V1
[9]
STRUCTURE AND EXPRESSION OF THE MOUSE APOLIPOPROTEIN C2 GENE [J].
HOFFER, MJV ;
VANECK, MM ;
HAVEKES, LM ;
HOFKER, MH ;
FRANTS, RR .
GENOMICS, 1993, 17 (01) :45-51
[10]
EVOLUTIONARY CONSERVATION OF THE MOUSE APOLIPOPROTEIN E-C1-C2 GENE-CLUSTER - STRUCTURE AND GENETIC-VARIABILITY IN INBRED MICE [J].
HOFFER, MJV ;
HOFKER, MH ;
VANECK, MM ;
HAVEKES, LM ;
FRANTS, RR .
GENOMICS, 1993, 15 (01) :62-67