Cargando…

The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida

BACKGROUND: Doubly uniparental inheritance (DUI) of mitochondrial DNA in bivalves is a fascinating exception to strictly maternal inheritance as practiced by all other animals. Recent work on DUI suggests that there may be unique regions of the mitochondrial genomes that play a role in sex determina...

Descripción completa

Detalles Bibliográficos
Autores principales: Chase, E. E., Robicheau, B. M., Veinot, S., Breton, S., Stewart, D. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870820/
https://www.ncbi.nlm.nih.gov/pubmed/29587633
http://dx.doi.org/10.1186/s12864-018-4583-3
_version_ 1783309553870307328
author Chase, E. E.
Robicheau, B. M.
Veinot, S.
Breton, S.
Stewart, D. T.
author_facet Chase, E. E.
Robicheau, B. M.
Veinot, S.
Breton, S.
Stewart, D. T.
author_sort Chase, E. E.
collection PubMed
description BACKGROUND: Doubly uniparental inheritance (DUI) of mitochondrial DNA in bivalves is a fascinating exception to strictly maternal inheritance as practiced by all other animals. Recent work on DUI suggests that there may be unique regions of the mitochondrial genomes that play a role in sex determination and/or sexual development in freshwater mussels (order Unionoida). In this study, one complete mitochondrial genome of the hermaphroditic swan mussel, Anodonta cygnea, is sequenced and compared to the complete mitochondrial genome of the gonochoric duck mussel, Anodonta anatina. An in silico assessment of novel proteins found within freshwater bivalve species (known as F-, H-, and M-open reading frames or ORFs) is conducted, with special attention to putative transmembrane domains (TMs), signal peptides (SPs), signal cleavage sites (SCS), subcellular localization, and potential control regions. Characteristics of TMs are also examined across freshwater mussel lineages. RESULTS: In silico analyses suggests the presence of SPs and SCSs and provides some insight into possible function(s) of these novel ORFs. The assessed confidence in these structures and functions was highly variable, possibly due to the novelty of these proteins. The number and topology of putative TMs appear to be maintained among both F- and H-ORFs, however, this is not the case for M-ORFs. There does not appear to be a typical control region in H-type mitochondrial DNA, especially given the loss of tandem repeats in unassigned regions when compared to F-type mtDNA. CONCLUSION: In silico analyses provides a useful tool to discover patterns in DUI and to navigate further in situ analyses related to DUI in freshwater mussels. In situ analysis will be necessary to further explore the intracellular localizations and possible role of these open reading frames in the process of sex determination in freshwater mussel. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4583-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5870820
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-58708202018-04-02 The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida Chase, E. E. Robicheau, B. M. Veinot, S. Breton, S. Stewart, D. T. BMC Genomics Research Article BACKGROUND: Doubly uniparental inheritance (DUI) of mitochondrial DNA in bivalves is a fascinating exception to strictly maternal inheritance as practiced by all other animals. Recent work on DUI suggests that there may be unique regions of the mitochondrial genomes that play a role in sex determination and/or sexual development in freshwater mussels (order Unionoida). In this study, one complete mitochondrial genome of the hermaphroditic swan mussel, Anodonta cygnea, is sequenced and compared to the complete mitochondrial genome of the gonochoric duck mussel, Anodonta anatina. An in silico assessment of novel proteins found within freshwater bivalve species (known as F-, H-, and M-open reading frames or ORFs) is conducted, with special attention to putative transmembrane domains (TMs), signal peptides (SPs), signal cleavage sites (SCS), subcellular localization, and potential control regions. Characteristics of TMs are also examined across freshwater mussel lineages. RESULTS: In silico analyses suggests the presence of SPs and SCSs and provides some insight into possible function(s) of these novel ORFs. The assessed confidence in these structures and functions was highly variable, possibly due to the novelty of these proteins. The number and topology of putative TMs appear to be maintained among both F- and H-ORFs, however, this is not the case for M-ORFs. There does not appear to be a typical control region in H-type mitochondrial DNA, especially given the loss of tandem repeats in unassigned regions when compared to F-type mtDNA. CONCLUSION: In silico analyses provides a useful tool to discover patterns in DUI and to navigate further in situ analyses related to DUI in freshwater mussels. In situ analysis will be necessary to further explore the intracellular localizations and possible role of these open reading frames in the process of sex determination in freshwater mussel. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4583-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-27 /pmc/articles/PMC5870820/ /pubmed/29587633 http://dx.doi.org/10.1186/s12864-018-4583-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chase, E. E.
Robicheau, B. M.
Veinot, S.
Breton, S.
Stewart, D. T.
The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida
title The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida
title_full The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida
title_fullStr The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida
title_full_unstemmed The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida
title_short The complete mitochondrial genome of the hermaphroditic freshwater mussel Anodonta cygnea (Bivalvia: Unionidae): in silico analyses of sex-specific ORFs across order Unionoida
title_sort complete mitochondrial genome of the hermaphroditic freshwater mussel anodonta cygnea (bivalvia: unionidae): in silico analyses of sex-specific orfs across order unionoida
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870820/
https://www.ncbi.nlm.nih.gov/pubmed/29587633
http://dx.doi.org/10.1186/s12864-018-4583-3
work_keys_str_mv AT chaseee thecompletemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT robicheaubm thecompletemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT veinots thecompletemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT bretons thecompletemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT stewartdt thecompletemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT chaseee completemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT robicheaubm completemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT veinots completemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT bretons completemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida
AT stewartdt completemitochondrialgenomeofthehermaphroditicfreshwatermusselanodontacygneabivalviaunionidaeinsilicoanalysesofsexspecificorfsacrossorderunionoida