SRC-1 and TIF2 control energy balance between white and brown adipose tissues

被引:375
作者
Picard, F
Géhin, M
Annicotte, JS
Rocchi, S
Champy, MF
O'Malley, BW
Chambon, P
Auwerx, J [1 ]
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[2] Inst Clin Souris Genopole Strasbourg, F-67404 Illkirch Graffenstaden, France
[3] Baylor Coll Med, Houston, TX 77030 USA
关键词
D O I
10.1016/S0092-8674(02)01169-8
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 explored the effects of two members of the p160 coregulator family on energy homeostasis. TIF2-/- mice are protected against obesity and display enhanced adaptive thermogenesis, whereas SRC-1-/- mice are prone to obesity due to reduced energy expenditure. In white adipose tissue, lack of TIF2 decreases PPARgamma activity and reduces fat accumulation, whereas in brown adipose tissue it facilitates the interaction between SRC-1 and PGC-1alpha, which induces PGC-1alpha's thermogenic activity. Interestingly, a high-fat diet increases the TIF2/SRC-1 expression ratio, which may contribute to weight gain. These results reveal that the relative level of TIF2/SRC-1 can modulate energy metabolism.
引用
收藏
页码:931 / 941
页数:11
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  • [1] Nuclear hormone receptors and gene expression
    Aranda, A
    Pascual, A
    [J]. PHYSIOLOGICAL REVIEWS, 2001, 81 (03) : 1269 - 1304
  • [2] Leptin and corticosterone have opposite effects on food intake and the expression of UCP1 mRNA in brown adipose tissue of lepob/lepob mice
    Arvaniti, K
    Ricquier, D
    Champigny, O
    Richard, D
    [J]. ENDOCRINOLOGY, 1998, 139 (09) : 4000 - 4003
  • [3] BLANCHETTEMACKIE EJ, 1995, J LIPID RES, V36, P1211
  • [4] PEROXISOME PROLIFERATOR AND RETINOID SIGNALING PATHWAYS COREGULATE PREADIPOCYTE PHENOTYPE AND SURVIVAL
    CHAWLA, A
    LAZAR, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (05) : 1786 - 1790
  • [5] Choi DS, 1997, DEVELOPMENT, V124, P1745
  • [6] Mutual synergistic folding in recruitment of CBP/p300 by p160 nuclear receptor coactivators
    Demarest, SJ
    Martinez-Yamout, M
    Chung, J
    Chen, HW
    Xu, W
    Dyson, HJ
    Evans, RM
    Wright, PE
    [J]. NATURE, 2002, 415 (6871) : 549 - 553
  • [7] Fajas L, 1999, MOL CELL BIOL, V19, P5495
  • [8] Transcription coactivator TRAP220 is required for PPARγ2-stimulated adipogenesis
    Ge, K
    Guermah, M
    Yuan, CX
    Ito, M
    Wallberg, AE
    Spiegelman, BM
    Roeder, RG
    [J]. NATURE, 2002, 417 (6888) : 563 - 567
  • [9] The function of TIF2/GRIP1 in mouse reproduction is distinct from those of SRC-1 and p/CIP
    Gehin, M
    Mark, M
    Dennefeld, C
    Dierich, A
    Gronemeyer, H
    Chambon, P
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (16) : 5923 - 5937
  • [10] p300 interacts with the N- and C-terminal part of PPARγ2 in a ligand-independent and -dependent manner, respectively
    Gelman, L
    Zhou, GC
    Fajas, L
    Raspé, E
    Fruchart, JC
    Auwerx, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) : 7681 - 7688