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PMID: 7574495 Published · ppublish English Journal Article Review

Transcriptional responses to polypeptide ligands: the JAK-STAT pathway.

Annual review of biochemistry ·Vol. 64 ·1995-00-00 ·Pages 621-51

Schindler C, Darnell JE

Abstract

Cytokines and growth factors regulate multiple aspects of cell growth through their interactions with specific receptors. These receptors initiate signals directed at both the cytoplasmic and the nuclear compartments. Many of the nuclear signals culminate in the induction of new genes. Characterization of the ability of IFN-alpha to rapidly induce new genes has led to the identification of a new signaling paradigm, the JAK-STAT (Signal Transducers and Activators of Transcription) pathway. In the IFN-alpha pathway, two receptor associated tyrosine kinases from the JAK family, Jak1 and Tyk2, mediate the activation of two latent cytoplasmic transcription factors, Stat1 and Stat2. More recent studies have not only determined that this pathway is used extensively, but have led to the identification of additional components (e.g., Jak2, Jak3, Stat3, Stat4, Stat5, and Stat6). This review will examine how these components mediate the transduction of signal directly from receptor to nucleus.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Binding Sites DNA/genetics,metabolism DNA-Binding Proteins/genetics,metabolism Humans Ligands Mice Molecular Sequence Data Phylogeny Protein-Tyrosine Kinases/genetics,metabolism Receptors, Cytokine/metabolism Signal Transduction Trans-Activators/genetics,metabolism Transcription, Genetic
Chemicals
DNA-Binding Proteins Ligands Receptors, Cytokine Trans-Activators DNA Protein-Tyrosine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Schindler C
Department of Medicine, Columbia University Medical Center, New York, N.Y., USA.
Darnell J E
Article Info
Journal
Annual review of biochemistry
Abbr.
Annu Rev Biochem
ISSN
0066-4154
Published
1995-00-00
Pages
621-51
Language
English
Region
United States
NLM ID
2985150R
Subset
IM
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