Abstract
Signal transducer and activator of transcription (STAT)-induced STAT inhibitor 1 (SSI-1) is known to function as a negative feedback regulator of cytokine signaling, but it is unclear whether it is involved in other biological events. Here, we show that SSI-1 participates and plays an important role in the insulin signal transduction pathway. SSI-1-deficient mice showed a significantly low level of blood sugar. While the forced expression of SSI-1 reduced the phosphorylation level of insulin receptor substrate 1 (IRS-1), SSI-1 deficiency resulted in sustained phosphorylation of IRS-1 in response to insulin.Furthermore, SSI-1 achieves this inhibition both by binding directly to IRS-1 and by suppressing Janus kinases. These findings suggest that SSI-1 acts as a negative feedback factor also in the insulin signal transduction pathway through the suppression of IRS-1 phosphorylation.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Base Sequence
-
Carrier Proteins / genetics
-
Carrier Proteins / metabolism*
-
DNA Primers / genetics
-
Feedback
-
Hypoglycemia / genetics
-
Hypoglycemia / metabolism
-
Insulin / metabolism*
-
Insulin / pharmacology
-
Insulin Receptor Substrate Proteins
-
JNK Mitogen-Activated Protein Kinases
-
Mice
-
Mice, Knockout
-
Mitogen-Activated Protein Kinases / antagonists & inhibitors
-
Phosphoproteins / metabolism*
-
Phosphorylation
-
RNA, Messenger / biosynthesis
-
RNA, Messenger / genetics
-
Repressor Proteins*
-
Signal Transduction
-
Suppressor of Cytokine Signaling 1 Protein
-
Suppressor of Cytokine Signaling Proteins
Substances
-
Carrier Proteins
-
DNA Primers
-
Insulin
-
Insulin Receptor Substrate Proteins
-
Irs1 protein, mouse
-
Phosphoproteins
-
RNA, Messenger
-
Repressor Proteins
-
Socs1 protein, mouse
-
Suppressor of Cytokine Signaling 1 Protein
-
Suppressor of Cytokine Signaling Proteins
-
JNK Mitogen-Activated Protein Kinases
-
Mitogen-Activated Protein Kinases