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Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network

BACKGROUND: BMPR-1B is part of the transforming growth factor β super family and plays a pivotal role in ewe litter size. Functional loss of exon-8 mutations in the BMPR-1B gene (namely the FecB gene) can increase both the ewe ovulation rate and litter size. RESULTS: This study constructed a eukaryo...

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Autores principales: Jia, Jianlei, Jin, Jipeng, Chen, Qian, Yuan, Zan, Li, Haiqin, Bian, Junhao, Gui, Linsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257232/
https://www.ncbi.nlm.nih.gov/pubmed/32471519
http://dx.doi.org/10.1186/s40659-020-00290-7
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author Jia, Jianlei
Jin, Jipeng
Chen, Qian
Yuan, Zan
Li, Haiqin
Bian, Junhao
Gui, Linsheng
author_facet Jia, Jianlei
Jin, Jipeng
Chen, Qian
Yuan, Zan
Li, Haiqin
Bian, Junhao
Gui, Linsheng
author_sort Jia, Jianlei
collection PubMed
description BACKGROUND: BMPR-1B is part of the transforming growth factor β super family and plays a pivotal role in ewe litter size. Functional loss of exon-8 mutations in the BMPR-1B gene (namely the FecB gene) can increase both the ewe ovulation rate and litter size. RESULTS: This study constructed a eukaryotic expression system, prepared a monoclonal antibody, and characterized BMPR-1B/FecB protein–protein interactions (PPIs). Using Co-immunoprecipitation coupled to mass spectrometry (Co-IP/MS), 23 proteins were identified that specifically interact with FecB in ovary extracts of ewes. Bioinformatics analysis of selected PPIs demonstrated that FecB associated with several other BMPs, primarily via signal transduction in the ovary. FecB and its associated interaction proteins enriched the reproduction process via BMP2 and BMP4 pathways. Signal transduction was identified via Smads proteins and TGF-beta signaling pathway by analyzing the biological processes and pathways. Moreover, other target proteins (GDF5, GDF9, RhoD, and HSP 10) that interact with FecB and that are related to ovulation and litter size in ewes were identified. CONCLUSIONS: In summary, this research identified a novel pathway and insight to explore the PPi network of BMPR-1B.
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spelling pubmed-72572322020-06-07 Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network Jia, Jianlei Jin, Jipeng Chen, Qian Yuan, Zan Li, Haiqin Bian, Junhao Gui, Linsheng Biol Res Research Article BACKGROUND: BMPR-1B is part of the transforming growth factor β super family and plays a pivotal role in ewe litter size. Functional loss of exon-8 mutations in the BMPR-1B gene (namely the FecB gene) can increase both the ewe ovulation rate and litter size. RESULTS: This study constructed a eukaryotic expression system, prepared a monoclonal antibody, and characterized BMPR-1B/FecB protein–protein interactions (PPIs). Using Co-immunoprecipitation coupled to mass spectrometry (Co-IP/MS), 23 proteins were identified that specifically interact with FecB in ovary extracts of ewes. Bioinformatics analysis of selected PPIs demonstrated that FecB associated with several other BMPs, primarily via signal transduction in the ovary. FecB and its associated interaction proteins enriched the reproduction process via BMP2 and BMP4 pathways. Signal transduction was identified via Smads proteins and TGF-beta signaling pathway by analyzing the biological processes and pathways. Moreover, other target proteins (GDF5, GDF9, RhoD, and HSP 10) that interact with FecB and that are related to ovulation and litter size in ewes were identified. CONCLUSIONS: In summary, this research identified a novel pathway and insight to explore the PPi network of BMPR-1B. BioMed Central 2020-05-29 /pmc/articles/PMC7257232/ /pubmed/32471519 http://dx.doi.org/10.1186/s40659-020-00290-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Jia, Jianlei
Jin, Jipeng
Chen, Qian
Yuan, Zan
Li, Haiqin
Bian, Junhao
Gui, Linsheng
Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network
title Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network
title_full Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network
title_fullStr Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network
title_full_unstemmed Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network
title_short Eukaryotic expression, Co-IP and MS identify BMPR-1B protein–protein interaction network
title_sort eukaryotic expression, co-ip and ms identify bmpr-1b protein–protein interaction network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257232/
https://www.ncbi.nlm.nih.gov/pubmed/32471519
http://dx.doi.org/10.1186/s40659-020-00290-7
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