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p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes

BACKGROUND: p14ARF is a protein product of the alternative reading frame of the human INK4a locus. It functions as a tumor suppressor protein. p14ARF suppresses growth through p53-dependent and p53-independent pathways. RESULTS: p14ARF protein localizes primarily to the nucleoli. Here we show that i...

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Autores principales: Kashuba, Elena, Mattsson, Karin, Klein, George, Szekely, Laszlo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC153488/
https://www.ncbi.nlm.nih.gov/pubmed/12685933
http://dx.doi.org/10.1186/1476-4598-2-18
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author Kashuba, Elena
Mattsson, Karin
Klein, George
Szekely, Laszlo
author_facet Kashuba, Elena
Mattsson, Karin
Klein, George
Szekely, Laszlo
author_sort Kashuba, Elena
collection PubMed
description BACKGROUND: p14ARF is a protein product of the alternative reading frame of the human INK4a locus. It functions as a tumor suppressor protein. p14ARF suppresses growth through p53-dependent and p53-independent pathways. RESULTS: p14ARF protein localizes primarily to the nucleoli. Here we show that in transfected cells p14ARF also appears in Hsp70 positive extranucleolar inclusions. The formation of p14ARF inclusions induces the parallel re-localization p53 and HDM2 to these sites that are also targeted by PML bodies and proteasomes. CONCLUSION: Our data show that co-localization between p53, HDM2 and p14ARF occurs at extranucleolar sites. Accumulation of PML and proteasomes at these sites suggest that the components of the nuclear inclusions are targeted for proteasome-mediated degradation.
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spelling pubmed-1534882003-04-19 p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes Kashuba, Elena Mattsson, Karin Klein, George Szekely, Laszlo Mol Cancer Research BACKGROUND: p14ARF is a protein product of the alternative reading frame of the human INK4a locus. It functions as a tumor suppressor protein. p14ARF suppresses growth through p53-dependent and p53-independent pathways. RESULTS: p14ARF protein localizes primarily to the nucleoli. Here we show that in transfected cells p14ARF also appears in Hsp70 positive extranucleolar inclusions. The formation of p14ARF inclusions induces the parallel re-localization p53 and HDM2 to these sites that are also targeted by PML bodies and proteasomes. CONCLUSION: Our data show that co-localization between p53, HDM2 and p14ARF occurs at extranucleolar sites. Accumulation of PML and proteasomes at these sites suggest that the components of the nuclear inclusions are targeted for proteasome-mediated degradation. BioMed Central 2003-03-05 /pmc/articles/PMC153488/ /pubmed/12685933 http://dx.doi.org/10.1186/1476-4598-2-18 Text en Copyright © 2003 Kashuba et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research
Kashuba, Elena
Mattsson, Karin
Klein, George
Szekely, Laszlo
p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes
title p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes
title_full p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes
title_fullStr p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes
title_full_unstemmed p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes
title_short p14ARF induces the relocation of HDM2 and p53 to extranucleolar sites that are targeted by PML bodies and proteasomes
title_sort p14arf induces the relocation of hdm2 and p53 to extranucleolar sites that are targeted by pml bodies and proteasomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC153488/
https://www.ncbi.nlm.nih.gov/pubmed/12685933
http://dx.doi.org/10.1186/1476-4598-2-18
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