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.
引用
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页码:173 / 177
页数:5
相关论文
共 36 条
  • [31] IRS-1 - ESSENTIAL FOR INSULIN-STIMULATED AND IL-4-STIMULATED MITOGENESIS IN HEMATOPOIETIC-CELLS
    WANG, LM
    MYERS, MG
    SUN, XJ
    AARONSON, SA
    WHITE, M
    PIERCE, JH
    [J]. SCIENCE, 1993, 261 (5128) : 1591 - 1594
  • [32] COMMON ELEMENTS IN INTERLEUKIN-4 AND INSULIN SIGNALING PATHWAYS IN FACTOR-DEPENDENT HEMATOPOIETIC-CELLS
    WANG, LM
    KEEGAN, AD
    LI, WQ
    LIENHARD, GE
    PACINI, S
    GUTKIND, JS
    MYERS, MG
    SUN, XJ
    WHITE, MF
    AARONSON, SA
    PAUL, WE
    PIERCE, JH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (09) : 4032 - 4036
  • [33] INTERLEUKIN-13 SIGNAL-TRANSDUCTION IN LYMPHOHEMATOPOIETIC CELLS - SIMILARITIES AND DIFFERENCES IN SIGNAL-TRANSDUCTION WITH INTERLEUKIN-4 AND INSULIN
    WELHAM, MJ
    LEARMONTH, L
    BONE, H
    SCHRADER, JW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (20) : 12286 - 12296
  • [34] MUTATION OF THE INSULIN-RECEPTOR AT TYROSINE-960 INHIBITS SIGNAL TRANSMISSION BUT DOES NOT AFFECT ITS TYROSINE KINASE-ACTIVITY
    WHITE, MF
    LIVINGSTON, JN
    BACKER, JM
    LAURIS, V
    DULL, TJ
    ULLRICH, A
    KAHN, CR
    [J]. CELL, 1988, 54 (05) : 641 - 649
  • [35] FORECASTING THE EDUCATIONAL-PARTICIPATION RATE OF 16-YEAR OLDS IN ENGLAND AND WALES - A SOCIOECONOMIC APPROACH
    WHITFIELD, K
    WILSON, RA
    [J]. INTERNATIONAL JOURNAL OF FORECASTING, 1991, 7 (01) : 65 - 76
  • [36] YONEZAWA K, 1994, J BIOL CHEM, V269, P4634