Mechanism of Inhibition of Growth Hormone Receptor Signaling by Suppressor of Cytokine Signaling Proteins
In this study we have investigated the role of suppressor of cytokine signaling (SOCS) proteins in GH receptor-mediated signaling. GH-induced transcription was inhibited by SOCS-1 and SOCS-3, while SOCS-2 and cytokine inducible SH2-containing protein (CIS) had no effect. By using chimeric SOCS prote...
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Veröffentlicht in: | Molecular endocrinology (Baltimore, Md.) Md.), 1999-11, Vol.13 (11), p.1832-1843 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study we have investigated the role
of suppressor of cytokine signaling (SOCS) proteins in GH
receptor-mediated signaling. GH-induced transcription was inhibited by
SOCS-1 and SOCS-3, while SOCS-2 and cytokine inducible SH2-containing
protein (CIS) had no effect. By using chimeric SOCS proteins it
was found that the ability of SOCS proteins to inhibit GH-mediated
transcription was located in the amino-terminal 40–80 amino acids. In
SOCS-3, 46 amino acids C-terminal to the SH2 domain were required for
the inhibitory activity, while a truncated SOCS-1 having only 2 amino
acids C-terminal to the SH2 domain was able to inhibit GH-mediated
transcription. Both SOCS-1 and SOCS-3 were able to inhibit GH-induced
STAT5 (signal transducer and activator of transcription)
activation. SOCS-1 inhibited the tyrosine kinase activity of Janus
kinase 2 (JAK2) directly, while SOCS-3 only inhibited JAK2 when
stimulated by the GH receptor. All four SOCS proteins were able to bind
to a tyrosine-phosphorylated glutathione-S-transferase-GH
receptor fusion protein, and SOCS-3 required the same 46 C-terminal
amino acids for GH receptor binding as it did for inhibition of
GH-mediated transcription and STAT5 activation. These data suggest that
SOCS-1 and -3 can suppress GH-induced transcriptional activity,
presumably by inhibiting the kinase activity of JAK2 either directly in
the case of SOCS-1 or via binding to the tyrosine-phosphorylated GH
receptor in the case of SOCS-3. |
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ISSN: | 0888-8809 1944-9917 |
DOI: | 10.1210/mend.13.11.0368 |