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CDK8 as the STAT1 serine 727 kinase?

Whereas cytokine-induced tyrosine phosphorylation of STAT (signal transducer and activator of transcription) proteins by JAK kinases has been well studied, much less is known about STAT-specific serine kinases and their signal-dependent regulation. The paper by Joanna Bancerek and colleagues publish...

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Detalles Bibliográficos
Autores principales: Staab, Julia, Herrmann-Lingen, Christoph, Meyer, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772107/
https://www.ncbi.nlm.nih.gov/pubmed/24069555
http://dx.doi.org/10.4161/jkst.24275
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author Staab, Julia
Herrmann-Lingen, Christoph
Meyer, Thomas
author_facet Staab, Julia
Herrmann-Lingen, Christoph
Meyer, Thomas
author_sort Staab, Julia
collection PubMed
description Whereas cytokine-induced tyrosine phosphorylation of STAT (signal transducer and activator of transcription) proteins by JAK kinases has been well studied, much less is known about STAT-specific serine kinases and their signal-dependent regulation. The paper by Joanna Bancerek and colleagues published recently in Immunity reports that upon interferon-γ (IFNγ) stimulation of cells the chromatin-associated cyclin-dependent kinase 8 (CDK8) phosphorylates the regulatory serine residue 727 in the transactivation domain of STAT1. The authors state that the CDK8 module of the Mediator complex is a key component in the STAT1 signal pathway, linking serine phosphorylation to gene-specific transcriptional events.
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spelling pubmed-37721072013-09-25 CDK8 as the STAT1 serine 727 kinase? Staab, Julia Herrmann-Lingen, Christoph Meyer, Thomas JAKSTAT Commentary Whereas cytokine-induced tyrosine phosphorylation of STAT (signal transducer and activator of transcription) proteins by JAK kinases has been well studied, much less is known about STAT-specific serine kinases and their signal-dependent regulation. The paper by Joanna Bancerek and colleagues published recently in Immunity reports that upon interferon-γ (IFNγ) stimulation of cells the chromatin-associated cyclin-dependent kinase 8 (CDK8) phosphorylates the regulatory serine residue 727 in the transactivation domain of STAT1. The authors state that the CDK8 module of the Mediator complex is a key component in the STAT1 signal pathway, linking serine phosphorylation to gene-specific transcriptional events. Landes Bioscience 2013-07-01 2013-08-15 /pmc/articles/PMC3772107/ /pubmed/24069555 http://dx.doi.org/10.4161/jkst.24275 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
Staab, Julia
Herrmann-Lingen, Christoph
Meyer, Thomas
CDK8 as the STAT1 serine 727 kinase?
title CDK8 as the STAT1 serine 727 kinase?
title_full CDK8 as the STAT1 serine 727 kinase?
title_fullStr CDK8 as the STAT1 serine 727 kinase?
title_full_unstemmed CDK8 as the STAT1 serine 727 kinase?
title_short CDK8 as the STAT1 serine 727 kinase?
title_sort cdk8 as the stat1 serine 727 kinase?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772107/
https://www.ncbi.nlm.nih.gov/pubmed/24069555
http://dx.doi.org/10.4161/jkst.24275
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