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Characterization of SET/I2PP2A Isoforms in Dogs
SET is an endogenous protein phosphatase 2A (PP2A) inhibitor and is associated with a poor prognosis in human leukemia. Previously, we reported increased SET protein levels in canine lymphoma cell lines and the potential therapeutic application of SET antagonists in canine lymphoma. Here, we found t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197151/ https://www.ncbi.nlm.nih.gov/pubmed/24897959 http://dx.doi.org/10.1292/jvms.14-0209 |
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author | YABE, Ryotaro FUJIWARA, Nobuyuki MIZUNO, Takuya USUI, Tatsuya OHAMA, Takashi SATO, Koichi |
author_facet | YABE, Ryotaro FUJIWARA, Nobuyuki MIZUNO, Takuya USUI, Tatsuya OHAMA, Takashi SATO, Koichi |
author_sort | YABE, Ryotaro |
collection | PubMed |
description | SET is an endogenous protein phosphatase 2A (PP2A) inhibitor and is associated with a poor prognosis in human leukemia. Previously, we reported increased SET protein levels in canine lymphoma cell lines and the potential therapeutic application of SET antagonists in canine lymphoma. Here, we found that canine cells express several isoforms of the SET protein. We cloned 4 isoforms of SET, named SETα, β, γ and δ. Genomic BLAST showed that the SET genes are located on chromosomes X, 7, 1 and 8, respectively. An immunofluorescent study showed nuclear localization of SETα and β, and nuclear and cytosolic localization of SETγ and δ. We confirmed that SETα and β possess the ability to associate with PP2A. Our data reveal the existence of unique SET isoforms that should be taken into account in SET-targeting drug development studies in dogs. |
format | Online Article Text |
id | pubmed-4197151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41971512014-10-17 Characterization of SET/I2PP2A Isoforms in Dogs YABE, Ryotaro FUJIWARA, Nobuyuki MIZUNO, Takuya USUI, Tatsuya OHAMA, Takashi SATO, Koichi J Vet Med Sci Pharmacology SET is an endogenous protein phosphatase 2A (PP2A) inhibitor and is associated with a poor prognosis in human leukemia. Previously, we reported increased SET protein levels in canine lymphoma cell lines and the potential therapeutic application of SET antagonists in canine lymphoma. Here, we found that canine cells express several isoforms of the SET protein. We cloned 4 isoforms of SET, named SETα, β, γ and δ. Genomic BLAST showed that the SET genes are located on chromosomes X, 7, 1 and 8, respectively. An immunofluorescent study showed nuclear localization of SETα and β, and nuclear and cytosolic localization of SETγ and δ. We confirmed that SETα and β possess the ability to associate with PP2A. Our data reveal the existence of unique SET isoforms that should be taken into account in SET-targeting drug development studies in dogs. The Japanese Society of Veterinary Science 2014-06-03 2014-09 /pmc/articles/PMC4197151/ /pubmed/24897959 http://dx.doi.org/10.1292/jvms.14-0209 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Pharmacology YABE, Ryotaro FUJIWARA, Nobuyuki MIZUNO, Takuya USUI, Tatsuya OHAMA, Takashi SATO, Koichi Characterization of SET/I2PP2A Isoforms in Dogs |
title | Characterization of SET/I2PP2A Isoforms in Dogs |
title_full | Characterization of SET/I2PP2A Isoforms in Dogs |
title_fullStr | Characterization of SET/I2PP2A Isoforms in Dogs |
title_full_unstemmed | Characterization of SET/I2PP2A Isoforms in Dogs |
title_short | Characterization of SET/I2PP2A Isoforms in Dogs |
title_sort | characterization of set/i2pp2a isoforms in dogs |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197151/ https://www.ncbi.nlm.nih.gov/pubmed/24897959 http://dx.doi.org/10.1292/jvms.14-0209 |
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