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Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin
Mitochondrial ORFans (open reading frames having no detectable homology and with unknown function) were discovered in bivalve molluscs with doubly uniparental inheritance (DUI) of mitochondria. In these animals, two mitochondrial lineages are present, one transmitted through eggs (F-type), the other...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942028/ https://www.ncbi.nlm.nih.gov/pubmed/24500970 http://dx.doi.org/10.1093/gbe/evu021 |
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author | Milani, Liliana Ghiselli, Fabrizio Maurizii, Maria Gabriella Nuzhdin, Sergey V. Passamonti, Marco |
author_facet | Milani, Liliana Ghiselli, Fabrizio Maurizii, Maria Gabriella Nuzhdin, Sergey V. Passamonti, Marco |
author_sort | Milani, Liliana |
collection | PubMed |
description | Mitochondrial ORFans (open reading frames having no detectable homology and with unknown function) were discovered in bivalve molluscs with doubly uniparental inheritance (DUI) of mitochondria. In these animals, two mitochondrial lineages are present, one transmitted through eggs (F-type), the other through sperm (M-type), each showing a specific ORFan. In this study, we used in situ hybridization and immunocytochemistry to provide evidence for the expression of Ruditapes philippinarum male-specific ORFan (orf21): both the transcript and the protein (RPHM21) were localized in spermatogenic cells and mature spermatozoa; the protein was localized in sperm mitochondria and nuclei, and in early embryos. Also, in silico analyses of orf21 flanking region and RPHM21 structure supported its derivation from viral sequence endogenization. We propose that RPHM21 prevents the recognition of M-type mitochondria by the degradation machinery, allowing their survival in the zygote. The process might involve a mechanism similar to that of Modulators of Immune Recognition, viral proteins involved in the immune recognition pathway, to which RPHM21 showed structural similarities. A viral origin of RPHM21 may also support a developmental role, because some integrated viral elements are involved in development and sperm differentiation of their host. Mitochondrial ORFans could be responsible for or participate in the DUI mechanism and their viral origin could explain the acquired capability of M-type mitochondria to avoid degradation and invade the germ line, that is what viruses do best: to elude host immune system and proliferate. |
format | Online Article Text |
id | pubmed-3942028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39420282014-03-04 Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin Milani, Liliana Ghiselli, Fabrizio Maurizii, Maria Gabriella Nuzhdin, Sergey V. Passamonti, Marco Genome Biol Evol Mitochondrial ORFans (open reading frames having no detectable homology and with unknown function) were discovered in bivalve molluscs with doubly uniparental inheritance (DUI) of mitochondria. In these animals, two mitochondrial lineages are present, one transmitted through eggs (F-type), the other through sperm (M-type), each showing a specific ORFan. In this study, we used in situ hybridization and immunocytochemistry to provide evidence for the expression of Ruditapes philippinarum male-specific ORFan (orf21): both the transcript and the protein (RPHM21) were localized in spermatogenic cells and mature spermatozoa; the protein was localized in sperm mitochondria and nuclei, and in early embryos. Also, in silico analyses of orf21 flanking region and RPHM21 structure supported its derivation from viral sequence endogenization. We propose that RPHM21 prevents the recognition of M-type mitochondria by the degradation machinery, allowing their survival in the zygote. The process might involve a mechanism similar to that of Modulators of Immune Recognition, viral proteins involved in the immune recognition pathway, to which RPHM21 showed structural similarities. A viral origin of RPHM21 may also support a developmental role, because some integrated viral elements are involved in development and sperm differentiation of their host. Mitochondrial ORFans could be responsible for or participate in the DUI mechanism and their viral origin could explain the acquired capability of M-type mitochondria to avoid degradation and invade the germ line, that is what viruses do best: to elude host immune system and proliferate. Oxford University Press 2014-02-05 /pmc/articles/PMC3942028/ /pubmed/24500970 http://dx.doi.org/10.1093/gbe/evu021 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Milani, Liliana Ghiselli, Fabrizio Maurizii, Maria Gabriella Nuzhdin, Sergey V. Passamonti, Marco Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin |
title | Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin |
title_full | Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin |
title_fullStr | Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin |
title_full_unstemmed | Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin |
title_short | Paternally Transmitted Mitochondria Express a New Gene of Potential Viral Origin |
title_sort | paternally transmitted mitochondria express a new gene of potential viral origin |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942028/ https://www.ncbi.nlm.nih.gov/pubmed/24500970 http://dx.doi.org/10.1093/gbe/evu021 |
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