ROLE OF IRS-2 IN INSULIN AND CYTOKINE SIGNALING

被引:755
作者
SUN, XJ
WANG, LM
ZHANG, YT
YENUSH, L
MYERS, MG
GLASHEEN, E
LANE, WS
PIERCE, JH
WHITE, MF
机构
[1] HARVARD UNIV,SCH MED,JOSLIN DIABET CTR,DIV RES,BOSTON,MA 02215
[2] HARVARD UNIV,SCH MED,DEPT MED,BOSTON,MA 02215
[3] NIH,CELL & MOLEC BIOL LAB,BETHESDA,MD 20892
[4] HARVARD UNIV,DEPT MOLEC & CELLULAR BIOL,HARVARD MICROCHEM FACIL,CAMBRIDGE,MA 02138
关键词
D O I
10.1038/377173a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
THE protein IRS-1 acts as an interface between signalling proteins with Src-homology-2 domains (SH2 proteins) and the receptors for insulin, IGF-1, growth hormone, several interleukins (IL-4, IL-9, IL-13) and other cytokines(1-7). It regulates gene expression acid stimulates mitogenesis, and appears to mediate insulin/IGF-1-stimulated glucose transport(8). Thus, survival of the IRS-1(-/-) mouse with only mild resistance to insulin was surprising(9,10). This dilemma is provisionally resolved with our discovery of a second IRS-signalling protein, We purified and cloned a likely candidate called 4PS from myeloid progenitor cells and, because of its resemblance to IRS-1, we designate it IRS-2. Alignment of the sequences of IRS-2 acid IRS-1 revealed a highly conserved amino terminus containing a pleckstrin-homology domain and a phosphotyrosine-binding domain, and a poorly conserved carboxy terminus containing several tyrosine phosphorylation motifs. IRS-2 is expressed in many cells, including tissues from IRS-1(-/-) mice(11), and may be essential for signalling by several receptor systems.
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页码:173 / 177
页数:5
相关论文
共 36 条
  • [21] PATTI ME, 1995, DIABETES, V44, pA31
  • [22] PERLMAN R, 1989, J BIOL CHEM, V264, P8946
  • [23] POTENT STIMULATION OF SH-PTP2 PHOSPHATASE-ACTIVITY BY SIMULTANEOUS OCCUPANCY OF BOTH SH2 DOMAINS
    PLUSKEY, S
    WANDLESS, TJ
    WALSH, CT
    SHOELSON, SE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (07) : 2897 - 2900
  • [24] GROWTH-HORMONE STIMULATES THE TYROSINE PHOSPHORYLATION OF THE INSULIN-RECEPTOR SUBSTRATE-1 AND ITS ASSOCIATION WITH PHOSPHATIDYLINOSITOL 3-KINASE IN PRIMARY ADIPOCYTES
    RIDDERSTRALE, M
    DEGERMAN, E
    TORNQVIST, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) : 3471 - 3474
  • [25] SUGIMOTO S, 1994, J BIOL CHEM, V269, P13614
  • [26] STRUCTURE OF THE INSULIN-RECEPTOR SUBSTRATE IRS-1 DEFINES A UNIQUE SIGNAL TRANSDUCTION PROTEIN
    SUN, XJ
    ROTHENBERG, P
    KAHN, CR
    BACKER, JM
    ARAKI, E
    WILDEN, PA
    CAHILL, DA
    GOLDSTEIN, BJ
    WHITE, MF
    [J]. NATURE, 1991, 352 (6330) : 73 - 77
  • [27] PLEIOTROPIC INSULIN SIGNALS ARE ENGAGED BY MULTISITE PHOSPHORYLATION OF IRS-1
    SUN, XJ
    CRIMMINS, DL
    MYERS, MG
    MIRALPEIX, M
    WHITE, MF
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) : 7418 - 7428
  • [28] SUN XJ, 1992, J BIOL CHEM, V267, P22662
  • [29] INSULIN-RESISTANCE AND GROWTH-RETARDATION IN MICE LACKING INSULIN-RECEPTOR SUBSTRATE-1
    TAMEMOTO, H
    KADOWAKI, T
    TOBE, K
    YAGI, T
    SAKURA, H
    HAYAKAWA, T
    TERAUCHI, Y
    UEKI, K
    KABURAGI, Y
    SATOH, S
    SEKIHARA, H
    YOSHIOKA, S
    HORIKOSHI, H
    FURUTA, Y
    IKAWA, Y
    KASUGA, M
    YAZAKI, Y
    AIZAWA, S
    [J]. NATURE, 1994, 372 (6502) : 182 - 186
  • [30] IL-4 ACTIVATES A DISTINCT SIGNAL TRANSDUCTION CASCADE FROM IL-3 IN FACTOR-DEPENDENT MYELOID CELLS
    WANG, LM
    KEEGAN, AD
    PAUL, WE
    HEIDARAN, MA
    GUTKIND, JS
    PIERCE, JH
    [J]. EMBO JOURNAL, 1992, 11 (13) : 4899 - 4908