ACTIVATION OF ACUTE-PHASE RESPONSE FACTOR (APRF)/STAT3 TRANSCRIPTION FACTOR BY GROWTH-HORMONE

被引:172
作者
CAMPBELL, GS
MEYER, DJ
RAZ, R
LEVY, DE
SCHWARTZ, J
CARTERSU, C
机构
[1] UNIV MICHIGAN,SCH MED,DEPT PHYSIOL,ANN ARBOR,MI 48109
[2] NYU,SCH MED,DEPT PATHOL,NEW YORK,NY 10016
[3] NYU,SCH MED,KAPLAN COMPREHENS CANC CTR,NEW YORK,NY 10016
关键词
D O I
10.1074/jbc.270.8.3974
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
The mechanisms by which the binding of growth hormone (GH) to its cell surface receptor elicits changes in gene transcription are largely unknown. The transcription factor Stat1/p91 has been shown to be activated by GH Here we show that acute phase response factor or Stat3 (or an antigenically related protein), is also activated by GH, Stats has been implicated in the interleukin-6-dependent induction of acute phase response genes, GH promotes in 3T3-F442A fibroblasts the tyrosyl phosphorylation of a protein immunoprecipitated by antibodies to Stats. This protein co-migrates with a tyrosyl phosphorylated protein from cells treated with leukemia inhibitory factor, a cytokine known 60 activate Stat3. Tyrosyl phosphorylated Stats is also observed in response to interferon-gamma. Stat3 is present in GH-inducible DNA-binding complexes that bind the sis-inducible element in the c-fos promoter and the acute phase response element in the alpha(2),-macroglobulin promoter. The ability of GH to activate both Stat1 and Stat3 (i.e. increase their tyrosyl phosphorylation and ability to bind to DNA) suggests that gene regulation by GH involves multiple Stat proteins. Shared transcription factors among hormones and cytokines that activate JAK kinases provide an explanation for shared responses, while the ability of the different Ligands to differentially recruit various Stat family members suggests mechanisms by which specificity in gene regulation could be achieved.
引用
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页码:3974 / 3979
页数:6
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