FOR, a novel orphan nuclear receptor related to farnesoid X receptor

被引:29
作者
Seo, YW
Sanyal, S
Kim, HJ
Won, DH
An, JY
Amano, T
Zavacki, AM
Kwon, HB
Shi, YB
Kim, WS
Kang, H
Moore, DD
Choi, HS [1 ]
机构
[1] Chonnam Natl Univ, Hormone Res Ctr, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Dept Biol, Kwangju 500757, South Korea
[3] Sogang Univ, Dept Life Sci, Seoul 121742, South Korea
[4] Seoul Natl Univ, Sch Earth & Environm Sci, Marine Biotechnol Lab, Seoul 151, South Korea
[5] NICHHD, Mol Embryol Lab, NIH, Bethesda, MD 20892 USA
[6] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Thyroid, Boston, MA 02115 USA
[7] Baylor Coll Med, Dept Cellular & Mol Biol, Houston, TX 77030 USA
关键词
D O I
10.1074/jbc.M111795200
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
We have identified and characterized a new amphibian orphan member of the nuclear receptor superfamily and termed it FOR1 (farnesoid X receptor (EXR)-like Orphan Receptor) because it shares the highest amino acid identity with the mammalian FXR. We also identified a variant of FOR1, called FOR2, which has 15 additional C-terminal amino acids. Both variants include an unusual insertion of 33 amino acids in the helix 7 region of the canonical ligand binding domain sequence, suggesting a unique structure for FOR. Northern blot analysis demonstrates that the FOR gene is highly expressed in adult and tadpole liver, kidney, and tail bud stage of the embryo. Detailed expression analysis using in situ hybridization indicates that FOR expression is first detectable at stage 30/31 in the presumptive liver region lasting until stage 41 with a peak level evident at stage 35/36. FOR forms heterodimeric complexes with retinoid X receptor (RXR) as demonstrated by biochemical and mammalian two-hybrid approaches. Gel mobility shift assays demonstrate that FORs form specific DNA-protein complexes on an FXR binding element consisting of an inverted repeat DNA element with 1 nucleotide spacing (IR1) from the phospholipid transfer protein gene promoter. Finally, although FORs do not exhibit constitutive transcriptional activity, frog gallbladder extract significantly augments the transcriptional activities of FORs.
引用
收藏
页码:17836 / 17844
页数:9
相关论文
共 35 条
[1]   A NEW ORPHAN MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY THAT INTERACTS WITH A SUBSET OF RETINOIC ACID RESPONSE ELEMENTS [J].
BAES, M ;
GULICK, T ;
CHOI, HS ;
MARTINOLI, MG ;
SIMHA, D ;
MOORE, DD .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1544-1552
[2]   Farnesoid X receptor responds to bile acids and represses cholesterol 7α-hydroxylase gene (CYP7A1) transcription [J].
Chiang, JYL ;
Kimmel, R ;
Weinberger, C ;
Stroup, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) :10918-10924
[3]   A NEW ORPHAN MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY CLOSELY-RELATED TO REV-ERB [J].
DUMAS, B ;
HARDING, HP ;
CHOI, HS ;
LEHMANN, KA ;
CHUNG, M ;
LAZAR, MA ;
MOORE, DD .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (08) :996-1005
[4]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[5]   IDENTIFICATION OF A NUCLEAR RECEPTOR THAT IS ACTIVATED BY FARNESOL METABOLITES [J].
FORMAN, BM ;
GOODE, E ;
CHEN, J ;
ORO, AE ;
BRADLEY, DJ ;
PERLMANN, T ;
NOONAN, DJ ;
BURKA, LT ;
MCMORRIS, T ;
LAMPH, WW ;
EVANS, RM ;
WEINBERGER, C .
CELL, 1995, 81 (05) :687-693
[6]   RETINOIC ACID RECEPTORS AND CELLULAR RETINOID-BINDING PROTEINS - COMPLEX INTERPLAY IN RETINOID SIGNALING [J].
GIGUERE, V .
ENDOCRINE REVIEWS, 1994, 15 (01) :61-79
[7]   IDENTIFICATION OF A NEW CLASS OF STEROID-HORMONE RECEPTORS [J].
GIGUERE, V ;
YANG, N ;
SEGUI, P ;
EVANS, RM .
NATURE, 1988, 331 (6151) :91-94
[8]   Orphan nuclear receptors:: From gene to function [J].
Giguère, V .
ENDOCRINE REVIEWS, 1999, 20 (05) :689-725
[9]   A regulatory cascade of the nuclear receptors FXR, SHP-1, and LRH-1 represses bile acid biosynthesis [J].
Goodwin, B ;
Jones, SA ;
Price, RR ;
Watson, MA ;
McKee, DD ;
Moore, LB ;
Galardi, C ;
Wilson, JG ;
Lewis, MC ;
Roth, ME ;
Maloney, PR ;
Willson, TM ;
Kliewer, SA .
MOLECULAR CELL, 2000, 6 (03) :517-526
[10]   Identification of a bile acid-responsive element in the human ileal bile acid-binding protein gene -: Involvement of the farnesoid X receptor/9-cis-retinoic acid receptor heterodimer [J].
Grober, J ;
Zaghini, I ;
Fujii, H ;
Jones, SA ;
Kliewer, SA ;
Willson, TM ;
Ono, T ;
Besnard, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) :29749-29754