Gene structure of pig sterol 12α-hydroxylase (CYP8B1) and expression in fetal liver:: comparison with expression of taurochenodeoxycholic acid 6α-hydroxylase (CYP4A21)

被引:7
|
作者
Lundell, K [1 ]
Wikvall, K [1 ]
机构
[1] Univ Uppsala, Dept Pharmaceut Biosci, Div Biochem, S-75123 Uppsala, Sweden
关键词
cytochrome P450; CYP8B1; CYP4A21; cholic acid; hyocholic acid; pig;
D O I
10.1016/j.bbalip.2003.09.002
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
Cholic acid is the major trihydroxy bile acid formed in most mammals. The domestic pig (Sus scrofa) is an exception. The bile of adult pig is devoid of cholic acid whereas hyocholic acid is found in amounts equal to that of cholic acid in humans. The pathway leading to formation of hyocholic acid is believed to be species-specific and to have evolved in the pig to compensate for a nonexistent or deficient cholic acid biosynthesis. However, a high level of cholic acid has recently been found in the bile of fetal pig. Here we describe that a gene encoding the key enzyme in cholic acid biosynthesis, the sterol 12alpha-hydroxylase (CYP8B1), is in fact present in the pig genome. The deduced amino acid sequence shows 81% identity to the human and rabbit orthologues. CYP8B1 mRNA is expressed at significant levels in fetal pig liver. Both CYP8B1 and the key enzyme in hyocholic acid formation, taurochenodeoxycholic acid 6alpha-hydroxylase (CYP4A21), were found to be expressed in pig liver in a developmental-dependent but opposite fashion. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:86 / 96
页数:11
相关论文
共 50 条
  • [1] Cloning and expression of a pig liver taurochenodeoxycholic acid 6α-hydroxylase (CYP4A21) -: A novel member of the CYP4A subfamily
    Lundell, K
    Hansson, R
    Wikvall, K
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) : 9606 - 9612
  • [2] The porcine taurochenodeoxycholic acid 6α-hydroxylase (CYP4A21) gene:: evolution by gene duplication and gene conversion
    Lundell, K
    BIOCHEMICAL JOURNAL, 2004, 378 : 1053 - 1058
  • [3] Cytokine regulation of human sterol 12α-hydroxylase (CYP8B1) gene
    Jahan, A
    Chiang, JYL
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 288 (04): : G685 - G695
  • [4] Differential hepatocellular zonation pattern of cholesterol 7α-hydroxylase (Cyp7a1) and sterol 12α-hydroxylase (Cyp8b1) in the mouse
    Jin Wang
    Maria Olin
    Björn Rozell
    Ingemar Björkhem
    Curt Einarsson
    Gösta Eggertsen
    Mats Gåfvels
    Histochemistry and Cell Biology, 2007, 127 : 253 - 261
  • [5] Differential hepatocellular zonation pattern of cholesterol 7α-hydroxylase (Cyp7a1) and sterol 12α-hydroxylase (Cyp8b1) in the mouse
    Wang, Jin
    Olin, Maria
    Rozell, Bjorn
    Bjorkhem, Ingemar
    Einarsson, Curt
    Eggertsen, Gosta
    Gafvels, Mats
    HISTOCHEMISTRY AND CELL BIOLOGY, 2007, 127 (03) : 253 - 261
  • [6] Mechanisms of cholesterol and sterol regulatory element binding protein regulation of the sterol 12α-hydroxylase gene (CYP8B1)
    Yang, YZ
    Eggertsen, G
    Gåfvels, M
    Andersson, U
    Einarsson, C
    Björkhem, I
    Chiang, JYL
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 320 (04) : 1204 - 1210
  • [7] Suppression of the Human Sterol 12α hydroxylase (CYP8B1) gene by Interleukin-1β (IL-1β)
    Jahan, A
    Zhang, M
    Chiang, JYL
    FASEB JOURNAL, 2003, 17 (04): : A240 - A240
  • [8] Suppression of the Human Sterol 12α hydroxylase (CYP8B1) gene by Interleukin-1β (IL-1β)
    Jahan, A
    Zhang, M
    Chiang, JYL
    FASEB JOURNAL, 2003, 17 (05): : A1342 - A1343
  • [9] Human sterol 12α-hydroxylase (CYP8B1) is mainly expressed in hepatocytes in a homogenous pattern
    Jin Wang
    Sinead Greene
    Lennart C. Eriksson
    Björn Rozell
    Eva Reihnér
    Curt Einarsson
    Gösta Eggertsen
    Mats Gåfvels
    Histochemistry and Cell Biology, 2005, 123 : 441 - 446
  • [10] Bile acids and FXR represses cholesterol 7A-hydroxylase (CYP7A1), sterol 12A-hydroxylase (CYP8B1) and sterol 27-hydroxylase (CYP27A1), but not oxysterol 7A-hydroxylase (CYP7B1) gene transcription.
    Chiang, JY
    Chen, W
    Zheng, M
    Wu, Z
    Kimmel, R
    Stroup, D
    GASTROENTEROLOGY, 2000, 118 (04) : A1006 - A1006