Literature DB >> 12208853

Biological evidence that SOCS-2 can act either as an enhancer or suppressor of growth hormone signaling.

Christopher J Greenhalgh1, Donald Metcalf, Anne L Thaus, Jason E Corbin, Rachel Uren, Phillip O Morgan, Louis J Fabri, Jian-Guo Zhang, Helene M Martin, Tracy A Willson, Nils Billestrup, Nicos A Nicola, Manuel Baca, Warren S Alexander, Douglas J Hilton.   

Abstract

Suppressor of cytokine signaling (SOCS)-2 is a member of a family of intracellular proteins implicated in the negative regulation of cytokine signaling. The generation of SOCS-2-deficient mice, which grow to one and a half times the size of their wild-type littermates, suggests that SOCS-2 may attenuate growth hormone (GH) signaling. In vitro studies indicate that, while SOCS-2 can inhibit GH action at low concentrations, at higher concentrations it may potentiate signaling. To determine whether a similar enhancement of signaling is observed in vivo or alternatively whether increased SOCS-2 levels repress growth in vivo, we generated and analyzed transgenic mice that overexpress SOCS-2 from a human ubiquitin C promoter. These mice are not growth-deficient and are, in fact, significantly larger than wild-type mice. The overexpressed SOCS-2 was found to bind to endogenous GH receptors in a number of mouse organs, while phosphopeptide binding studies with recombinant SOCS-2 defined phosphorylated tyrosine 595 on the GH receptor as the site of interaction. Together, the data implicate SOCS-2 as having dual effects on GH signaling in vivo.

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Year:  2002        PMID: 12208853     DOI: 10.1074/jbc.C200450200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  45 in total

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