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Interactome of the negative regulator of nuclear import BRCA1-binding protein 2
Although the negative regulator of nuclear import (NRNI) BRCA1 binding protein 2 (BRAP2) is highly expressed in testis, its role is largely unknown. Here we address this question by documenting the BRAP2 interactome from human testis, using the yeast 2-hybrid system to identify BRAP2-interacting pro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377634/ https://www.ncbi.nlm.nih.gov/pubmed/25820252 http://dx.doi.org/10.1038/srep09459 |
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author | Fatima, Shadma Wagstaff, Kylie M. Loveland, Kate L. Jans, David A. |
author_facet | Fatima, Shadma Wagstaff, Kylie M. Loveland, Kate L. Jans, David A. |
author_sort | Fatima, Shadma |
collection | PubMed |
description | Although the negative regulator of nuclear import (NRNI) BRCA1 binding protein 2 (BRAP2) is highly expressed in testis, its role is largely unknown. Here we address this question by documenting the BRAP2 interactome from human testis, using the yeast 2-hybrid system to identify BRAP2-interacting proteins with roles in diverse cellular processes, including regulation of the actin cytoskeleton, ubiquitinylation, cell cycle/apoptosis and transcription. Interaction with BRAP2 in adult mouse testis with three of these, PH domain and leucine rich repeat protein phosphatase 1 (PHLPP1), A-Kinase anchor protein (AKAP3) and DNA methyl transferase 1 (DNMT1), was confirmed by coimmunoprecipitation assays. BRAP2's ability to inhibit PHLPP1 and DNMT1 nuclear localisation was also confirmed by quantitative confocal microscopy. Importantly, the physiological relevance thereof was implied by the cytoplasmic localisation of PHLPP1, AKAP3 and DNMT1 in pachytene spermatocytes/round spermatids where BRAP2 is present at high levels, and nuclear localisation of PHLPP1 and DNMT1 in spermatogonia concomitant with lower levels of BRAP2. Interestingly, BRAP2 was also present in murine spermatozoa, in part colocalised with AKAP3. Together the results indicate for the first time that BRAP2 may play an important NRNI role in germ cells of the testis, with an additional, scaffold/structural role in mature spermatozoa. |
format | Online Article Text |
id | pubmed-4377634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43776342015-04-07 Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 Fatima, Shadma Wagstaff, Kylie M. Loveland, Kate L. Jans, David A. Sci Rep Article Although the negative regulator of nuclear import (NRNI) BRCA1 binding protein 2 (BRAP2) is highly expressed in testis, its role is largely unknown. Here we address this question by documenting the BRAP2 interactome from human testis, using the yeast 2-hybrid system to identify BRAP2-interacting proteins with roles in diverse cellular processes, including regulation of the actin cytoskeleton, ubiquitinylation, cell cycle/apoptosis and transcription. Interaction with BRAP2 in adult mouse testis with three of these, PH domain and leucine rich repeat protein phosphatase 1 (PHLPP1), A-Kinase anchor protein (AKAP3) and DNA methyl transferase 1 (DNMT1), was confirmed by coimmunoprecipitation assays. BRAP2's ability to inhibit PHLPP1 and DNMT1 nuclear localisation was also confirmed by quantitative confocal microscopy. Importantly, the physiological relevance thereof was implied by the cytoplasmic localisation of PHLPP1, AKAP3 and DNMT1 in pachytene spermatocytes/round spermatids where BRAP2 is present at high levels, and nuclear localisation of PHLPP1 and DNMT1 in spermatogonia concomitant with lower levels of BRAP2. Interestingly, BRAP2 was also present in murine spermatozoa, in part colocalised with AKAP3. Together the results indicate for the first time that BRAP2 may play an important NRNI role in germ cells of the testis, with an additional, scaffold/structural role in mature spermatozoa. Nature Publishing Group 2015-03-30 /pmc/articles/PMC4377634/ /pubmed/25820252 http://dx.doi.org/10.1038/srep09459 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fatima, Shadma Wagstaff, Kylie M. Loveland, Kate L. Jans, David A. Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 |
title | Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 |
title_full | Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 |
title_fullStr | Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 |
title_full_unstemmed | Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 |
title_short | Interactome of the negative regulator of nuclear import BRCA1-binding protein 2 |
title_sort | interactome of the negative regulator of nuclear import brca1-binding protein 2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377634/ https://www.ncbi.nlm.nih.gov/pubmed/25820252 http://dx.doi.org/10.1038/srep09459 |
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