SOCS-6 binds to insulin receptor substrate 4, and mice lacking the SOCS-6 gene exhibit mild growth retardation

Krebs, DL; Uren, RT; Metcalf, D; Rakar, S; Zhang, JG; Starr, R; De Souza, DP; Hanzinikolas, K; Eyles, J; Connolly, LM; Simpson, RJ; Nicola, NA; Nicholson, SE; Baca, M; Hilton, DJ; Alexander, WS

Author(s): Krebs, DL; Uren, RT; Metcalf, D; Rakar, S; Zhang, JG; Starr, R; De Souza, DP; Hanzinikolas, K; Eyles, J; Connolly, LM; Simpson, RJ; Nicola, NA; Nicholson, SE; Baca, M; Hilton, DJ; Alexander, WS;
Details: Publication Year 2002-07,Volume 22,Issue #13,Page 4567-4578
Journal Title: MOLECULAR AND CELLULAR BIOLOGY
Publication Type: Journal Article
Abstract: SOCS-6 is a member of the suppressor of cytokine signaling (SOCS) family, of proteins (SOCS-1 to SOCS-7 and CIS) which each contain a central SH2 domain and a carboxyl-terminal SOCS box. SOCS-1, SOCS-2, SOCS-3, and CIS act to negatively regulate cytokine-induced signaling pathways; however, the actions of SOCS-4, SOCS-5, SOCS-6, and SOCS-7 remain less clear. Here we have used both biochemical and genetic approaches to examine the action of SOCS-6. We found that SOCS-6 and SOCS-7 are expressed ubiquitously in murine tissues. Like other SOCS family members, SOCS-6 binds to elongins B and C through its SOCS box, suggesting that it might act as an E3 ubiquitin ligase that targets proteins bound to its SH2 domain for ubiquitination and proteasomal degradation. We investigated the binding specificity, of the SOCS-6 and SOCS-7 SH2 domains and found that they preferentially bound to phosphopeptides containing a valine in the phosphotyrosine (pY) +1 position and a hydrophobic residue in the pY +2 and pY +3 positions. In addition, these SH2 domains interacted with a protein complex consisting of insulin receptor substrate 4 (IRS-4), IRS-2, and the p85 regulatory subunit of phosphatidylinositol 3-kinase. To investigate the physiological role of SOCS-6, we generated mice lacking the SOCS-6 gene. SOCS-6(-/-) mice were born in a normal Mendelian ratio, were fertile, developed normally, and did not exhibit defects in hernatopoiesis or glucose homeostasis. However, both male and female SOCS-6(-/-) mice weighed approximately 10% less than wild-type littermates.
Publisher: AMER SOC MICROBIOLOGY
Keywords: JANUS TYROSINE KINASE; CYTOKINE SIGNALING-1; SH2 DOMAIN; BOX MOTIF; PROTEIN; SUPPRESSOR; INHIBITION; TRANSDUCTION; DEGRADATION; CELLS
Publisher's Version: https://doi.org/10.1128/MCB.22.13.4567-4578.2002
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Creation Date: 2002-07-01 12:00:00