Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fatima, Shadma, Wagstaff, Kylie M., Loveland, Kate L., Jans, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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
_version_ 1782363943370489856
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
work_keys_str_mv AT fatimashadma interactomeofthenegativeregulatorofnuclearimportbrca1bindingprotein2
AT wagstaffkyliem interactomeofthenegativeregulatorofnuclearimportbrca1bindingprotein2
AT lovelandkatel interactomeofthenegativeregulatorofnuclearimportbrca1bindingprotein2
AT jansdavida interactomeofthenegativeregulatorofnuclearimportbrca1bindingprotein2