CHARACTERIZATION OF THE CHICKEN APOLIPOPROTEIN-A-I GENE 5'-FLANKING REGION

被引:10
|
作者
BHATTACHARYYA, N
CHATTAPADHYAY, R
ODDOUX, C
BANERJEE, D
机构
[1] NEW YORK BLOOD CTR,LINDSLEY F KIMBALL RES INST,DEPT MEMBRANE BIOCHEM,310 E 67TH ST,NEW YORK,NY 10021
[2] NYU,SCH MED,DEPT PHARMACOL,NEW YORK,NY 10016
关键词
D O I
10.1089/dna.1993.12.597
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 A-I (apoA-I) is a major protein component of plasma high-density lipoprotein in all species studied, and plays an important role in cholesterol homeostasis. In an earlier study, we cloned and structurally characterized the chicken apoA-I gene. In this study, the 5'-flanking region of the chicken apoA-I gene was sequenced and functionally characterized. Sequence analysis of the 510-nucleotide 5' upstream region revealed the presence of TATA and CCAAT boxes. In addition, we identified binding sites for several transcription factors such as Sp1, AP1, and NF1.2. When the 5' fragment was ligated into a promoterless CAT vector and transfected into a chicken hepatocarcinoma cell line (LMH), the bacterial chloramphenicol acetyl transferase (CAT) gene was expressed, suggesting transcriptional regulation is associated with this region. Transfection studies with other 5' deletion constructs revealed that the sequence spanning the region -82 to +87 contained the major transcriptional activity. DNase I footprinting, gel retardation, and Southwestern blot analyses showed that the fragment interacts with nuclear proteins.
引用
收藏
页码:597 / 604
页数:8
相关论文
共 50 条
  • [1] CHARACTERIZATION OF POLYMORPHISMS IN THE 5'-FLANKING REGION OF THE APOLIPOPROTEIN(A) GENE AMONG INDIVIDUALS
    ICHINOSE, A
    [J]. THROMBOSIS AND HAEMOSTASIS, 1993, 69 (06) : 1097 - 1097
  • [2] ISOLATION AND CHARACTERIZATION OF THE HUMAN APOLIPOPROTEIN-A-I GENE
    KARATHANASIS, SK
    ZANNIS, VI
    BRESLOW, JL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (20): : 6147 - 6151
  • [3] DETECTION OF POLYMORPHISMS IN THE 5'-FLANKING REGION OF THE GENE FOR APOLIPOPROTEIN(A)
    ICHINOSE, A
    KURIYAMA, M
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 209 (01) : 372 - 378
  • [4] Characterization of the 5′-flanking transcriptional regulatory region of chicken growth hormone gene
    Ip, SCY
    Lau, JS
    Au, WL
    Leung, FC
    [J]. EXPERIMENTAL BIOLOGY AND MEDICINE, 2004, 229 (07) : 640 - 649
  • [5] Polymorphisms of 5′ flanking region of chicken prolactin gene
    Liang, Y
    Cui, JX
    Yang, GF
    Leung, FCC
    Zhang, XQ
    [J]. DOMESTIC ANIMAL ENDOCRINOLOGY, 2006, 30 (01) : 1 - 16
  • [6] IDENTIFICATION OF THE AP1-RELATED SITES IN HUMAN APOLIPOPROTEIN-A-I GENE 5'-FLANKING REGION, RESPONSIBLE FOR TISSUE-SPECIFIC REPRESSION
    KONDRASHOV, AV
    ALENIN, VV
    PEREVOZCHIKOV, AP
    [J]. DOKLADY AKADEMII NAUK, 1994, 335 (05) : 643 - 645
  • [7] APOLIPOPROTEIN-A-I GENE POLYMORPHISM IN THE 3' FLANKING REGION ASSOCIATED WITH FAMILIAL HYPOALPHALIPOPROTEINEMIA AND PREMATURE CORONARY-ARTERY DISEASE
    ORDOVAS, JM
    SCHAEFER, EJ
    SALEM, D
    GLUECK, CJ
    VERGANI, C
    WILSON, PWF
    KARATHANASIS, SK
    [J]. ARTERIOSCLEROSIS, 1985, 5 (05): : A505 - A505
  • [8] STRUCTURE, EVOLUTION, AND REGULATION OF CHICKEN APOLIPOPROTEIN-A-I
    RAJAVASHISTH, TB
    DAWSON, PA
    WILLIAMS, DL
    SHACKELFORD, JE
    LEBHERZ, H
    LUSIS, AJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1987, 262 (15) : 7058 - 7065
  • [9] CHICKEN TYROSINE-HYDROXYLASE GENE - ISOLATION AND FUNCTIONAL-CHARACTERIZATION OF THE 5' FLANKING REGION
    CARRIER, A
    DEVIGNES, MD
    RENOIR, D
    AUFFRAY, C
    [J]. JOURNAL OF NEUROCHEMISTRY, 1993, 61 (06) : 2215 - 2224
  • [10] APOLIPOPROTEIN-A-I DEFICIENCY DUE TO A CODON-84 NONSENSE MUTATION OF THE APOLIPOPROTEIN-A-I GENE
    MATSUNAGA, T
    HIASA, Y
    YANAGI, H
    MAEDA, T
    HATTORI, N
    YAMAKAWA, K
    YAMANOUCHI, Y
    TANAKA, I
    OBARA, T
    HAMAGUCHI, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (07) : 2793 - 2797