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The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development
Coordination of mitochondrial and nuclear processes is key to the cellular health; however, very little is known about the molecular mechanisms regulating nuclear-mitochondrial crosstalk. Here, we report a novel molecular mechanism controlling the shuttling of CREB (cAMP response element-binding pro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287909/ https://www.ncbi.nlm.nih.gov/pubmed/37144466 http://dx.doi.org/10.1093/nar/gkad343 |
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author | Bhuiyan, Sayem H Bordet, Guillaume Bamgbose, Gbolahan Tulin, Alexei V |
author_facet | Bhuiyan, Sayem H Bordet, Guillaume Bamgbose, Gbolahan Tulin, Alexei V |
author_sort | Bhuiyan, Sayem H |
collection | PubMed |
description | Coordination of mitochondrial and nuclear processes is key to the cellular health; however, very little is known about the molecular mechanisms regulating nuclear-mitochondrial crosstalk. Here, we report a novel molecular mechanism controlling the shuttling of CREB (cAMP response element-binding protein) protein complex between mitochondria and nucleoplasm. We show that a previously unknown protein, herein termed as Jig, functions as a tissue-specific and developmental timing-specific coregulator in the CREB pathway. Our results demonstrate that Jig shuttles between mitochondria and nucleoplasm, interacts with CrebA protein and controls its delivery to the nucleus, thus triggering CREB-dependent transcription in nuclear chromatin and mitochondria. Ablating the expression of Jig prevents CrebA from localizing to the nucleoplasm, affecting mitochondrial functioning and morphology and leads to Drosophila developmental arrest at the early third instar larval stage. Together, these results implicate Jig as an essential mediator of nuclear and mitochondrial processes. We also found that Jig belongs to a family of nine similar proteins, each of which has its own tissue- and time-specific expression profile. Thus, our results are the first to describe the molecular mechanism regulating nuclear and mitochondrial processes in a tissue- and time-specific manner. |
format | Online Article Text |
id | pubmed-10287909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102879092023-06-24 The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development Bhuiyan, Sayem H Bordet, Guillaume Bamgbose, Gbolahan Tulin, Alexei V Nucleic Acids Res Molecular Biology Coordination of mitochondrial and nuclear processes is key to the cellular health; however, very little is known about the molecular mechanisms regulating nuclear-mitochondrial crosstalk. Here, we report a novel molecular mechanism controlling the shuttling of CREB (cAMP response element-binding protein) protein complex between mitochondria and nucleoplasm. We show that a previously unknown protein, herein termed as Jig, functions as a tissue-specific and developmental timing-specific coregulator in the CREB pathway. Our results demonstrate that Jig shuttles between mitochondria and nucleoplasm, interacts with CrebA protein and controls its delivery to the nucleus, thus triggering CREB-dependent transcription in nuclear chromatin and mitochondria. Ablating the expression of Jig prevents CrebA from localizing to the nucleoplasm, affecting mitochondrial functioning and morphology and leads to Drosophila developmental arrest at the early third instar larval stage. Together, these results implicate Jig as an essential mediator of nuclear and mitochondrial processes. We also found that Jig belongs to a family of nine similar proteins, each of which has its own tissue- and time-specific expression profile. Thus, our results are the first to describe the molecular mechanism regulating nuclear and mitochondrial processes in a tissue- and time-specific manner. Oxford University Press 2023-05-05 /pmc/articles/PMC10287909/ /pubmed/37144466 http://dx.doi.org/10.1093/nar/gkad343 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Molecular Biology Bhuiyan, Sayem H Bordet, Guillaume Bamgbose, Gbolahan Tulin, Alexei V The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development |
title | The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development |
title_full | The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development |
title_fullStr | The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development |
title_full_unstemmed | The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development |
title_short | The Drosophila gene encoding JIG protein (CG14850) is critical for CrebA nuclear trafficking during development |
title_sort | drosophila gene encoding jig protein (cg14850) is critical for creba nuclear trafficking during development |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287909/ https://www.ncbi.nlm.nih.gov/pubmed/37144466 http://dx.doi.org/10.1093/nar/gkad343 |
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