Life without white fat: a transgenic mouse

被引:612
作者
Moitra, J
Mason, MM
Olive, M
Krylov, D
Gavrilova, O
Marcus-Samuels, B
Feigenbaum, L
Lee, E
Aoyama, T
Eckhaus, M
Reitman, ML [1 ]
Vinson, C
机构
[1] NIDDKD, Diabet Branch, Bethesda, MD 20892 USA
[2] NCI, Biochem Lab, Bethesda, MD 20892 USA
[3] NICHHD, Lab Mammalian Genes & Dev, Bethesda, MD 20892 USA
[4] NIH, Vet Resources Program, Off Res Serv, Bethesda, MD 20892 USA
[5] NCI, Frederick Canc Res & Dev Ctr, Sci Applicat Int Corp, Frederick, MD 21702 USA
[6] Shinshu Univ, Sch Med, Dept Biochem, Matsumoto, Nagano 390, Japan
关键词
AP-1; C/EBP; dominant negative proteins; adipocytes; lipodystrophy; diabetes;
D O I
10.1101/gad.12.20.3168
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have generated a transgenic mouse with no white fat tissue throughout life. These mice express a dominant-negative protein, termed A-ZIP/F, under the control of the adipose-specific aP2 enhancer/promoter. This protein prevents the DNA binding of B-ZIP transcription factors of both the C/EBP and Tun families. The transgenic mice (named A-ZIP/F-1) have no white adipose tissue and dramatically reduced amounts of brown adipose tissue, which is inactive. They are initially growth delayed, but by week 12, surpass their littermates in weight. The mice eat, drink, and urinate copiously, have decreased fecundity, premature death, and frequently die after anesthesia. The physiological consequences of having no white fat tissue are profound. The liver is engorged with lipid, and the internal organs are enlarged. The mice are diabetic, with reduced leptin (20-fold) and elevated serum glucose (3-fold), insulin (50- to 400-fold), free fatty acids (2-fold), and triglycerides (3- to 5-fold). The A-ZIP/F-1 phenotype suggests a mouse model for the human disease lipoatrophic diabetes (Seip-Berardinelli syndrome), indicating that the lack of fat can cause diabetes. The myriad of consequences of having no fat throughout development can be addressed with this model.
引用
收藏
页码:3168 / 3181
页数:14
相关论文
共 77 条
  • [1] A dominant-negative inhibitor of CREB reveals that it is a general mediator of stimulus-dependent transcription of c-fos
    Ahn, S
    Olive, M
    Aggarwal, S
    Krylov, D
    Ginty, DD
    Vinson, C
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) : 967 - 977
  • [2] AILAUD G, 1998, HDB OBESITY, P359
  • [3] Altman DG, 1990, PRACTICAL STAT MED R
  • [4] [Anonymous], 1994, MANIPULATING MOUSE E
  • [5] Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor α (PPARα)
    Aoyama, T
    Peters, JM
    Iritani, N
    Nakajima, T
    Furihata, K
    Hashimoto, T
    Gonzalez, FJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) : 5678 - 5684
  • [6] PEROXISOMAL ACYL COENZYME-A OXIDASE IS A RATE-LIMITING ENZYME IN A VERY-LONG-CHAIN FATTY-ACID BETA-OXIDATION SYSTEM
    AOYAMA, T
    SOURI, M
    KAMIJO, T
    USHIKUBO, S
    HASHIMOTO, T
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 201 (03) : 1541 - 1547
  • [7] Ausubel F.A., 1997, CURRENT PROTOCOLS MO, DOI DOI 10.1.4
  • [8] Insulin stimulates both leptin secretion and production by rat white adipose tissue
    Barr, VA
    Malide, D
    Zarnowski, MJ
    Taylor, SI
    Cushman, SW
    [J]. ENDOCRINOLOGY, 1997, 138 (10) : 4463 - 4472
  • [9] MINI-MOUSE - PHENOTYPIC CHARACTERIZATION OF A TRANSGENIC INSERTIONAL MUTANT ALLELIC TO PYGMY
    BENSON, KF
    CHADA, K
    [J]. GENETICAL RESEARCH, 1994, 64 (01) : 27 - 33
  • [10] TISSUE SPECIFIC EXPRESSION OF P422 PROTEIN, A PUTATIVE LIPID CARRIER, IN MOUSE ADIPOCYTES
    BERNLOHR, DA
    DOERING, TL
    KELLY, TJ
    LANE, MD
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 132 (02) : 850 - 855