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New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET
Human CISD2 and mitoNEET are two NEET proteins anchored in the endoplasmic reticulum and mitochondria membranes respectively, with an Fe–S containing domain stretching out in the cytosol. Their cytosolic domains are close in sequence and structure. In the present study, combining cellular and bioche...
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/PMC8067432/ https://www.ncbi.nlm.nih.gov/pubmed/33916457 http://dx.doi.org/10.3390/biomedicines9040384 |
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author | Salameh, Myriam Riquier, Sylvie Guittet, Olivier Huang, Meng-Er Vernis, Laurence Lepoivre, Michel Golinelli-Cohen, Marie-Pierre |
author_facet | Salameh, Myriam Riquier, Sylvie Guittet, Olivier Huang, Meng-Er Vernis, Laurence Lepoivre, Michel Golinelli-Cohen, Marie-Pierre |
author_sort | Salameh, Myriam |
collection | PubMed |
description | Human CISD2 and mitoNEET are two NEET proteins anchored in the endoplasmic reticulum and mitochondria membranes respectively, with an Fe–S containing domain stretching out in the cytosol. Their cytosolic domains are close in sequence and structure. In the present study, combining cellular and biochemical approaches, we compared both proteins in order to possibly identify specific roles and mechanisms of action in the cell. We show that both proteins exhibit a high intrinsic stability and a sensitivity of their cluster to oxygen. In contrast, they differ in according to expression profiles in tissues and intracellular half-life. The stability of their Fe–S cluster and its ability to be transferred in vitro are affected differently by pH variations in a physiological and pathological range for cytosolic pH. Finally, we question a possible role for CISD2 in cellular Fe–S cluster trafficking. In conclusion, our work highlights unexpected major differences in the cellular and biochemical features between these two structurally close NEET proteins. |
format | Online Article Text |
id | pubmed-8067432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80674322021-04-25 New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET Salameh, Myriam Riquier, Sylvie Guittet, Olivier Huang, Meng-Er Vernis, Laurence Lepoivre, Michel Golinelli-Cohen, Marie-Pierre Biomedicines Article Human CISD2 and mitoNEET are two NEET proteins anchored in the endoplasmic reticulum and mitochondria membranes respectively, with an Fe–S containing domain stretching out in the cytosol. Their cytosolic domains are close in sequence and structure. In the present study, combining cellular and biochemical approaches, we compared both proteins in order to possibly identify specific roles and mechanisms of action in the cell. We show that both proteins exhibit a high intrinsic stability and a sensitivity of their cluster to oxygen. In contrast, they differ in according to expression profiles in tissues and intracellular half-life. The stability of their Fe–S cluster and its ability to be transferred in vitro are affected differently by pH variations in a physiological and pathological range for cytosolic pH. Finally, we question a possible role for CISD2 in cellular Fe–S cluster trafficking. In conclusion, our work highlights unexpected major differences in the cellular and biochemical features between these two structurally close NEET proteins. MDPI 2021-04-05 /pmc/articles/PMC8067432/ /pubmed/33916457 http://dx.doi.org/10.3390/biomedicines9040384 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 Salameh, Myriam Riquier, Sylvie Guittet, Olivier Huang, Meng-Er Vernis, Laurence Lepoivre, Michel Golinelli-Cohen, Marie-Pierre New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET |
title | New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET |
title_full | New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET |
title_fullStr | New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET |
title_full_unstemmed | New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET |
title_short | New Insights of the NEET Protein CISD2 Reveals Distinct Features Compared to Its Close Mitochondrial Homolog mitoNEET |
title_sort | new insights of the neet protein cisd2 reveals distinct features compared to its close mitochondrial homolog mitoneet |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067432/ https://www.ncbi.nlm.nih.gov/pubmed/33916457 http://dx.doi.org/10.3390/biomedicines9040384 |
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