Cargando…

Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules

BACKGROUND: DZIP1 (DAZ-interacting protein 1) has been described as a component of the Hh signaling pathway with a putative regulatory role in ciliogenesis. DZIP1 interacts with DAZ RNA binding proteins in embryonic stem cells and human germ cells suggesting a role in mRNA regulation. RESULTS: We in...

Descripción completa

Detalles Bibliográficos
Autores principales: ShigunovShigunov, Patrícia, Sotelo-Silveira, Jose, Stimamiglio, Marco Augusto, Kuligovski, Crisciele, Irigoín, Florencia, Badano, Jose L, Munroe, David, Correa, Alejandro, Dallagiovanna, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091656/
https://www.ncbi.nlm.nih.gov/pubmed/24993635
http://dx.doi.org/10.1186/1471-2199-15-12
_version_ 1782480789371355136
author ShigunovShigunov, Patrícia
Sotelo-Silveira, Jose
Stimamiglio, Marco Augusto
Kuligovski, Crisciele
Irigoín, Florencia
Badano, Jose L
Munroe, David
Correa, Alejandro
Dallagiovanna, Bruno
author_facet ShigunovShigunov, Patrícia
Sotelo-Silveira, Jose
Stimamiglio, Marco Augusto
Kuligovski, Crisciele
Irigoín, Florencia
Badano, Jose L
Munroe, David
Correa, Alejandro
Dallagiovanna, Bruno
author_sort ShigunovShigunov, Patrícia
collection PubMed
description BACKGROUND: DZIP1 (DAZ-interacting protein 1) has been described as a component of the Hh signaling pathway with a putative regulatory role in ciliogenesis. DZIP1 interacts with DAZ RNA binding proteins in embryonic stem cells and human germ cells suggesting a role in mRNA regulation. RESULTS: We investigated DZIP1 function in HeLa cells and its involvement in ribonucleoprotein complexes. DZIP1 was predominantly located in granules in the cytoplasm. Under oxidative stress conditions, DZIP1 re-localized to stress granules. DZIP appears to be important for the formation of stress granules during the stress response. We used immunoprecipitation assays with antibodies against DZIP1 and microarray hybridization to identify mRNAs associated with DZIP1. The genetic networks formed by the DZIP1-associated mRNAs were involved in cell cycle and gene expression regulation. DZIP1 is involved in the Hedgehog signaling pathway. We used cyclopamine, a specific inhibitor of this pathway, to analyze the expression of DZIP1 and its associated mRNAs. The abundance of DZIP1-associated mRNAs increased with treatment; however, the silencing or overexpression of DZIP1 in HeLa cells had no effect on the accumulation of the associated mRNAs. Polysomal profile analysis by sucrose gradient centrifugation demonstrated the presence of DZIP1 in the polysomal fraction. CONCLUSIONS: Our results suggest that DZIP1 is part of an RNP complex that occupies various subcellular locations. The diversity of the mRNAs associated with DZIP1 suggests that this protein is a component of different RNPs associated with translating polysomes and with RNA granules.
format Online
Article
Text
id pubmed-4091656
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40916562014-07-11 Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules ShigunovShigunov, Patrícia Sotelo-Silveira, Jose Stimamiglio, Marco Augusto Kuligovski, Crisciele Irigoín, Florencia Badano, Jose L Munroe, David Correa, Alejandro Dallagiovanna, Bruno BMC Mol Biol Research Article BACKGROUND: DZIP1 (DAZ-interacting protein 1) has been described as a component of the Hh signaling pathway with a putative regulatory role in ciliogenesis. DZIP1 interacts with DAZ RNA binding proteins in embryonic stem cells and human germ cells suggesting a role in mRNA regulation. RESULTS: We investigated DZIP1 function in HeLa cells and its involvement in ribonucleoprotein complexes. DZIP1 was predominantly located in granules in the cytoplasm. Under oxidative stress conditions, DZIP1 re-localized to stress granules. DZIP appears to be important for the formation of stress granules during the stress response. We used immunoprecipitation assays with antibodies against DZIP1 and microarray hybridization to identify mRNAs associated with DZIP1. The genetic networks formed by the DZIP1-associated mRNAs were involved in cell cycle and gene expression regulation. DZIP1 is involved in the Hedgehog signaling pathway. We used cyclopamine, a specific inhibitor of this pathway, to analyze the expression of DZIP1 and its associated mRNAs. The abundance of DZIP1-associated mRNAs increased with treatment; however, the silencing or overexpression of DZIP1 in HeLa cells had no effect on the accumulation of the associated mRNAs. Polysomal profile analysis by sucrose gradient centrifugation demonstrated the presence of DZIP1 in the polysomal fraction. CONCLUSIONS: Our results suggest that DZIP1 is part of an RNP complex that occupies various subcellular locations. The diversity of the mRNAs associated with DZIP1 suggests that this protein is a component of different RNPs associated with translating polysomes and with RNA granules. BioMed Central 2014-07-03 /pmc/articles/PMC4091656/ /pubmed/24993635 http://dx.doi.org/10.1186/1471-2199-15-12 Text en Copyright © 2014 Shigunov et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
ShigunovShigunov, Patrícia
Sotelo-Silveira, Jose
Stimamiglio, Marco Augusto
Kuligovski, Crisciele
Irigoín, Florencia
Badano, Jose L
Munroe, David
Correa, Alejandro
Dallagiovanna, Bruno
Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules
title Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules
title_full Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules
title_fullStr Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules
title_full_unstemmed Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules
title_short Ribonomic analysis of human DZIP1 reveals its involvement in ribonucleoprotein complexes and stress granules
title_sort ribonomic analysis of human dzip1 reveals its involvement in ribonucleoprotein complexes and stress granules
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091656/
https://www.ncbi.nlm.nih.gov/pubmed/24993635
http://dx.doi.org/10.1186/1471-2199-15-12
work_keys_str_mv AT shigunovshigunovpatricia ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT sotelosilveirajose ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT stimamigliomarcoaugusto ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT kuligovskicrisciele ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT irigoinflorencia ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT badanojosel ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT munroedavid ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT correaalejandro ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules
AT dallagiovannabruno ribonomicanalysisofhumandzip1revealsitsinvolvementinribonucleoproteincomplexesandstressgranules