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DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP

mRNA decay mediated by the AU-rich elements (AREs) is one of the most studied post-transcriptional mechanisms and is modulated by ARE-binding proteins (ARE-BPs). To understand the regulation of K homology splicing regulatory protein (KSRP), a decay-promoting ARE-BP, we purified KSRP protein complexe...

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Autores principales: Chou, Chu-Fang, Lin, Wei-Jye, Lin, Chen-Chung, Luber, Christian A., Godbout, Roseline, Mann, Matthias, Chen, Ching-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762726/
https://www.ncbi.nlm.nih.gov/pubmed/24023901
http://dx.doi.org/10.1371/journal.pone.0073752
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author Chou, Chu-Fang
Lin, Wei-Jye
Lin, Chen-Chung
Luber, Christian A.
Godbout, Roseline
Mann, Matthias
Chen, Ching-Yi
author_facet Chou, Chu-Fang
Lin, Wei-Jye
Lin, Chen-Chung
Luber, Christian A.
Godbout, Roseline
Mann, Matthias
Chen, Ching-Yi
author_sort Chou, Chu-Fang
collection PubMed
description mRNA decay mediated by the AU-rich elements (AREs) is one of the most studied post-transcriptional mechanisms and is modulated by ARE-binding proteins (ARE-BPs). To understand the regulation of K homology splicing regulatory protein (KSRP), a decay-promoting ARE-BP, we purified KSRP protein complexes and identified an RNA helicase, DDX1. We showed that down-regulation of DDX1 expression elevated cytoplasmic levels of KSRP and facilitated ARE-mediated mRNA decay. Association of KSRP with 14-3-3 proteins, that are predominately located in the cytoplasm, increased upon reduction of DDX1. We also demonstrated that KSRP associated with DDX1 or 14-3-3, but not both. These observations indicate that subcellular localization of KSRP is regulated by competing interactions with DDX1 or 14-3-3.
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spelling pubmed-37627262013-09-10 DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP Chou, Chu-Fang Lin, Wei-Jye Lin, Chen-Chung Luber, Christian A. Godbout, Roseline Mann, Matthias Chen, Ching-Yi PLoS One Research Article mRNA decay mediated by the AU-rich elements (AREs) is one of the most studied post-transcriptional mechanisms and is modulated by ARE-binding proteins (ARE-BPs). To understand the regulation of K homology splicing regulatory protein (KSRP), a decay-promoting ARE-BP, we purified KSRP protein complexes and identified an RNA helicase, DDX1. We showed that down-regulation of DDX1 expression elevated cytoplasmic levels of KSRP and facilitated ARE-mediated mRNA decay. Association of KSRP with 14-3-3 proteins, that are predominately located in the cytoplasm, increased upon reduction of DDX1. We also demonstrated that KSRP associated with DDX1 or 14-3-3, but not both. These observations indicate that subcellular localization of KSRP is regulated by competing interactions with DDX1 or 14-3-3. Public Library of Science 2013-09-04 /pmc/articles/PMC3762726/ /pubmed/24023901 http://dx.doi.org/10.1371/journal.pone.0073752 Text en © 2013 Chou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chou, Chu-Fang
Lin, Wei-Jye
Lin, Chen-Chung
Luber, Christian A.
Godbout, Roseline
Mann, Matthias
Chen, Ching-Yi
DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP
title DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP
title_full DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP
title_fullStr DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP
title_full_unstemmed DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP
title_short DEAD Box Protein DDX1 Regulates Cytoplasmic Localization of KSRP
title_sort dead box protein ddx1 regulates cytoplasmic localization of ksrp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762726/
https://www.ncbi.nlm.nih.gov/pubmed/24023901
http://dx.doi.org/10.1371/journal.pone.0073752
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