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D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria
The MTERF protein family comprises members from Metazoans and plants. All the Metazoan MTERF proteins characterized to date, including the mitochondrial transcription termination factors, play a key role in mitochondrial gene expression. In this study we report the characterization of Drosophila MTE...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447168/ https://www.ncbi.nlm.nih.gov/pubmed/22784680 http://dx.doi.org/10.1016/j.mito.2012.06.010 |
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author | Bruni, Francesco Manzari, Caterina Filice, Mariacristina Loguercio Polosa, Paola Colella, Matilde Carmone, Claudia Hambardjieva, Elena Garcia-Diaz, Miguel Cantatore, Palmiro Roberti, Marina |
author_facet | Bruni, Francesco Manzari, Caterina Filice, Mariacristina Loguercio Polosa, Paola Colella, Matilde Carmone, Claudia Hambardjieva, Elena Garcia-Diaz, Miguel Cantatore, Palmiro Roberti, Marina |
author_sort | Bruni, Francesco |
collection | PubMed |
description | The MTERF protein family comprises members from Metazoans and plants. All the Metazoan MTERF proteins characterized to date, including the mitochondrial transcription termination factors, play a key role in mitochondrial gene expression. In this study we report the characterization of Drosophila MTERF5 (D-MTERF5), a mitochondrial protein existing only in insects, probably originated from a duplication event of the transcription termination factor DmTTF. D-MTERF5 knock-down in D.Mel-2 cells alters transcript levels with an opposite pattern to that produced by DmTTF knock-down. D-MTERF5 is able to interact with mtDNA at the same sites contacted by DmTTF, but only in the presence of the termination factor. We propose that the two proteins participate in the transcription termination process, with D-MTERF5 engaged in relieving the block exerted by DmTTF. This hypothesis is supported also by D-MTERF5 homology modeling, which suggests that this protein contains protein–protein interaction domains. Co-regulation by DREF (DNA Replication-related Element binding Factor) of D-MTERF5 and DmTTF implies that expression of the two factors needs to be co-ordinated to ensure fine modulation of Drosophila mitochondrial transcription. |
format | Online Article Text |
id | pubmed-3447168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34471682012-09-26 D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria Bruni, Francesco Manzari, Caterina Filice, Mariacristina Loguercio Polosa, Paola Colella, Matilde Carmone, Claudia Hambardjieva, Elena Garcia-Diaz, Miguel Cantatore, Palmiro Roberti, Marina Mitochondrion Article The MTERF protein family comprises members from Metazoans and plants. All the Metazoan MTERF proteins characterized to date, including the mitochondrial transcription termination factors, play a key role in mitochondrial gene expression. In this study we report the characterization of Drosophila MTERF5 (D-MTERF5), a mitochondrial protein existing only in insects, probably originated from a duplication event of the transcription termination factor DmTTF. D-MTERF5 knock-down in D.Mel-2 cells alters transcript levels with an opposite pattern to that produced by DmTTF knock-down. D-MTERF5 is able to interact with mtDNA at the same sites contacted by DmTTF, but only in the presence of the termination factor. We propose that the two proteins participate in the transcription termination process, with D-MTERF5 engaged in relieving the block exerted by DmTTF. This hypothesis is supported also by D-MTERF5 homology modeling, which suggests that this protein contains protein–protein interaction domains. Co-regulation by DREF (DNA Replication-related Element binding Factor) of D-MTERF5 and DmTTF implies that expression of the two factors needs to be co-ordinated to ensure fine modulation of Drosophila mitochondrial transcription. Elsevier Science 2012-09 /pmc/articles/PMC3447168/ /pubmed/22784680 http://dx.doi.org/10.1016/j.mito.2012.06.010 Text en © 2012 Elsevier B.V. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) . |
spellingShingle | Article Bruni, Francesco Manzari, Caterina Filice, Mariacristina Loguercio Polosa, Paola Colella, Matilde Carmone, Claudia Hambardjieva, Elena Garcia-Diaz, Miguel Cantatore, Palmiro Roberti, Marina D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria |
title | D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria |
title_full | D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria |
title_fullStr | D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria |
title_full_unstemmed | D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria |
title_short | D-MTERF5 is a novel factor modulating transcription in Drosophila mitochondria |
title_sort | d-mterf5 is a novel factor modulating transcription in drosophila mitochondria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447168/ https://www.ncbi.nlm.nih.gov/pubmed/22784680 http://dx.doi.org/10.1016/j.mito.2012.06.010 |
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