Cargando…

Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene

BACKGROUND: Mitochondria mediate most of the energy production that occurs in the majority of eukaryotic organisms. These subcellular organelles contain a genome that differs from the nuclear genome and is referred to as mitochondrial DNA (mtDNA). Despite a disparity in gene content, all mtDNAs enco...

Descripción completa

Detalles Bibliográficos
Autores principales: Faure, Eric, Delaye, Luis, Tribolo, Sandra, Levasseur, Anthony, Seligmann, Hervé, Barthélémy, Roxane-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214167/
https://www.ncbi.nlm.nih.gov/pubmed/22024028
http://dx.doi.org/10.1186/1745-6150-6-56
_version_ 1782216213892431872
author Faure, Eric
Delaye, Luis
Tribolo, Sandra
Levasseur, Anthony
Seligmann, Hervé
Barthélémy, Roxane-Marie
author_facet Faure, Eric
Delaye, Luis
Tribolo, Sandra
Levasseur, Anthony
Seligmann, Hervé
Barthélémy, Roxane-Marie
author_sort Faure, Eric
collection PubMed
description BACKGROUND: Mitochondria mediate most of the energy production that occurs in the majority of eukaryotic organisms. These subcellular organelles contain a genome that differs from the nuclear genome and is referred to as mitochondrial DNA (mtDNA). Despite a disparity in gene content, all mtDNAs encode at least two components of the mitochondrial electron transport chain, including cytochrome c oxidase I (Cox1). PRESENTATION OF THE HYPOTHESIS: A positionally conserved ORF has been found on the complementary strand of the cox1 genes of both eukaryotic mitochondria (protist, plant, fungal and animal) and alpha-proteobacteria. This putative gene has been named gau for gene antisense ubiquitous in mtDNAs. The length of the deduced protein is approximately 100 amino acids. In vertebrates, several stop codons have been found in the mt gau region, and potentially functional gau regions have been found in nuclear genomes. However, a recent bioinformatics study showed that several hypothetical overlapping mt genes could be predicted, including gau; this involves the possible import of the cytosolic AGR tRNA into the mitochondria and/or the expression of mt antisense tRNAs with anticodons recognizing AGR codons according to an alternative genetic code that is induced by the presence of suppressor tRNAs. Despite an evolutionary distance of at least 1.5 to 2.0 billion years, the deduced Gau proteins share some conserved amino acid signatures and structure, which suggests a possible conserved function. Moreover, BLAST analysis identified rare, sense-oriented ESTs with poly(A) tails that include the entire gau region. Immunohistochemical analyses using an anti-Gau monoclonal antibody revealed strict co-localization of Gau proteins and a mitochondrial marker. TESTING THE HYPOTHESIS: This hypothesis could be tested by purifying the gau gene product and determining its sequence. Cell biological experiments are needed to determine the physiological role of this protein. IMPLICATIONS OF THE HYPOTHESIS: Studies of the gau ORF will shed light on the origin of novel genes and their functions in organelles and could also have medical implications for human diseases that are caused by mitochondrial dysfunction. Moreover, this strengthens evidence for mitochondrial genes coded according to an overlapping genetic code.
format Online
Article
Text
id pubmed-3214167
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-32141672011-11-12 Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene Faure, Eric Delaye, Luis Tribolo, Sandra Levasseur, Anthony Seligmann, Hervé Barthélémy, Roxane-Marie Biol Direct Hypothesis BACKGROUND: Mitochondria mediate most of the energy production that occurs in the majority of eukaryotic organisms. These subcellular organelles contain a genome that differs from the nuclear genome and is referred to as mitochondrial DNA (mtDNA). Despite a disparity in gene content, all mtDNAs encode at least two components of the mitochondrial electron transport chain, including cytochrome c oxidase I (Cox1). PRESENTATION OF THE HYPOTHESIS: A positionally conserved ORF has been found on the complementary strand of the cox1 genes of both eukaryotic mitochondria (protist, plant, fungal and animal) and alpha-proteobacteria. This putative gene has been named gau for gene antisense ubiquitous in mtDNAs. The length of the deduced protein is approximately 100 amino acids. In vertebrates, several stop codons have been found in the mt gau region, and potentially functional gau regions have been found in nuclear genomes. However, a recent bioinformatics study showed that several hypothetical overlapping mt genes could be predicted, including gau; this involves the possible import of the cytosolic AGR tRNA into the mitochondria and/or the expression of mt antisense tRNAs with anticodons recognizing AGR codons according to an alternative genetic code that is induced by the presence of suppressor tRNAs. Despite an evolutionary distance of at least 1.5 to 2.0 billion years, the deduced Gau proteins share some conserved amino acid signatures and structure, which suggests a possible conserved function. Moreover, BLAST analysis identified rare, sense-oriented ESTs with poly(A) tails that include the entire gau region. Immunohistochemical analyses using an anti-Gau monoclonal antibody revealed strict co-localization of Gau proteins and a mitochondrial marker. TESTING THE HYPOTHESIS: This hypothesis could be tested by purifying the gau gene product and determining its sequence. Cell biological experiments are needed to determine the physiological role of this protein. IMPLICATIONS OF THE HYPOTHESIS: Studies of the gau ORF will shed light on the origin of novel genes and their functions in organelles and could also have medical implications for human diseases that are caused by mitochondrial dysfunction. Moreover, this strengthens evidence for mitochondrial genes coded according to an overlapping genetic code. BioMed Central 2011-10-24 /pmc/articles/PMC3214167/ /pubmed/22024028 http://dx.doi.org/10.1186/1745-6150-6-56 Text en Copyright ©2011 Faure et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hypothesis
Faure, Eric
Delaye, Luis
Tribolo, Sandra
Levasseur, Anthony
Seligmann, Hervé
Barthélémy, Roxane-Marie
Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene
title Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene
title_full Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene
title_fullStr Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene
title_full_unstemmed Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene
title_short Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene
title_sort probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase i gene
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214167/
https://www.ncbi.nlm.nih.gov/pubmed/22024028
http://dx.doi.org/10.1186/1745-6150-6-56
work_keys_str_mv AT faureeric probablepresenceofanubiquitouscrypticmitochondrialgeneontheantisensestrandofthecytochromeoxidaseigene
AT delayeluis probablepresenceofanubiquitouscrypticmitochondrialgeneontheantisensestrandofthecytochromeoxidaseigene
AT tribolosandra probablepresenceofanubiquitouscrypticmitochondrialgeneontheantisensestrandofthecytochromeoxidaseigene
AT levasseuranthony probablepresenceofanubiquitouscrypticmitochondrialgeneontheantisensestrandofthecytochromeoxidaseigene
AT seligmannherve probablepresenceofanubiquitouscrypticmitochondrialgeneontheantisensestrandofthecytochromeoxidaseigene
AT barthelemyroxanemarie probablepresenceofanubiquitouscrypticmitochondrialgeneontheantisensestrandofthecytochromeoxidaseigene