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Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147
Nuclear envelope (NE) and endoplasmic reticulum (ER) collaborate to control a multitude of nuclear and cytoplasmic actions. In this context, the transmembrane protein TMEM147 localizes to both NE and ER, and through direct and indirect interactions regulates processes as varied as production and tra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508377/ https://www.ncbi.nlm.nih.gov/pubmed/34638576 http://dx.doi.org/10.3390/ijms221910231 |
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author | Maimaris, Giannis Christodoulou, Andri Santama, Niovi Lederer, Carsten Werner |
author_facet | Maimaris, Giannis Christodoulou, Andri Santama, Niovi Lederer, Carsten Werner |
author_sort | Maimaris, Giannis |
collection | PubMed |
description | Nuclear envelope (NE) and endoplasmic reticulum (ER) collaborate to control a multitude of nuclear and cytoplasmic actions. In this context, the transmembrane protein TMEM147 localizes to both NE and ER, and through direct and indirect interactions regulates processes as varied as production and transport of multipass membrane proteins, neuronal signaling, nuclear-shape, lamina and chromatin dynamics and cholesterol synthesis. Aiming to delineate the emerging multifunctionality of TMEM147 more comprehensively, we set as objectives, first, to assess potentially more fundamental effects of TMEM147 on the ER and, second, to identify significantly TMEM147-associated cell-wide protein networks and pathways. Quantifying curved and flat ER markers RTN4 and CLIMP63/CKAP4, respectively, we found that TMEM147 silencing causes area and intensity increases for both RTN4 and CLIMP63, and the ER in general, with a profound shift toward flat areas, concurrent with reduction in DNA condensation. Protein network and pathway analyses based on comprehensive compilation of TMEM147 interactors, targets and co-factors then served to manifest novel and established roles for TMEM147. Thus, algorithmically simplified significant pathways reflect TMEM147 function in ribosome binding, oxidoreductase activity, G protein-coupled receptor activity and transmembrane transport, while analysis of protein factors and networks identifies hub proteins and corresponding pathways as potential targets of TMEM147 action and of future functional studies. |
format | Online Article Text |
id | pubmed-8508377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85083772021-10-13 Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 Maimaris, Giannis Christodoulou, Andri Santama, Niovi Lederer, Carsten Werner Int J Mol Sci Article Nuclear envelope (NE) and endoplasmic reticulum (ER) collaborate to control a multitude of nuclear and cytoplasmic actions. In this context, the transmembrane protein TMEM147 localizes to both NE and ER, and through direct and indirect interactions regulates processes as varied as production and transport of multipass membrane proteins, neuronal signaling, nuclear-shape, lamina and chromatin dynamics and cholesterol synthesis. Aiming to delineate the emerging multifunctionality of TMEM147 more comprehensively, we set as objectives, first, to assess potentially more fundamental effects of TMEM147 on the ER and, second, to identify significantly TMEM147-associated cell-wide protein networks and pathways. Quantifying curved and flat ER markers RTN4 and CLIMP63/CKAP4, respectively, we found that TMEM147 silencing causes area and intensity increases for both RTN4 and CLIMP63, and the ER in general, with a profound shift toward flat areas, concurrent with reduction in DNA condensation. Protein network and pathway analyses based on comprehensive compilation of TMEM147 interactors, targets and co-factors then served to manifest novel and established roles for TMEM147. Thus, algorithmically simplified significant pathways reflect TMEM147 function in ribosome binding, oxidoreductase activity, G protein-coupled receptor activity and transmembrane transport, while analysis of protein factors and networks identifies hub proteins and corresponding pathways as potential targets of TMEM147 action and of future functional studies. MDPI 2021-09-23 /pmc/articles/PMC8508377/ /pubmed/34638576 http://dx.doi.org/10.3390/ijms221910231 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Maimaris, Giannis Christodoulou, Andri Santama, Niovi Lederer, Carsten Werner Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 |
title | Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 |
title_full | Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 |
title_fullStr | Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 |
title_full_unstemmed | Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 |
title_short | Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147 |
title_sort | regulation of er composition and extent, and putative action in protein networks by er/ne protein tmem147 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508377/ https://www.ncbi.nlm.nih.gov/pubmed/34638576 http://dx.doi.org/10.3390/ijms221910231 |
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