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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...

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Autores principales: Salameh, Myriam, Riquier, Sylvie, Guittet, Olivier, Huang, Meng-Er, Vernis, Laurence, Lepoivre, Michel, Golinelli-Cohen, Marie-Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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