A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE
Angiotensin-converting enzyme (ACE) is a highly conserved metallopeptidase. In mammals, the somatic isoform governs blood pressure whereas the germinal isoform (tACE) is required for fertility. In Ecdysozoans, ACE-like enzymes are implicated in reproduction. Despite ACE orthologues being present fro...
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ftpubmed:oai:pubmedcentral.nih.gov:3235092 2023-05-15T15:58:17+02:00 A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE Riviere, Guillaume Fellous, Alexandre Franco, Alban Bernay, Benoit Favrel, Pascal 2011-12-09 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235092 http://www.ncbi.nlm.nih.gov/pubmed/22174750 https://doi.org/10.1371/journal.pone.0027833 en eng Public Library of Science http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235092 http://www.ncbi.nlm.nih.gov/pubmed/22174750 http://dx.doi.org/10.1371/journal.pone.0027833 Riviere et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. CC-BY Research Article Text 2011 ftpubmed https://doi.org/10.1371/journal.pone.0027833 2013-09-03T23:46:51Z Angiotensin-converting enzyme (ACE) is a highly conserved metallopeptidase. In mammals, the somatic isoform governs blood pressure whereas the germinal isoform (tACE) is required for fertility. In Ecdysozoans, ACE-like enzymes are implicated in reproduction. Despite ACE orthologues being present from bacteria to humans, their function(s) remain(s) unknown in distant organisms such as Lophotrochozoans. In silico analysis of an oyster (Crassostrea gigas) EST library suggested the presence of an ACE orthologue in molluscs. Primer walking and 5′-RACE revealed that the 1.9 kb cDNA encodes CgACE, a 632 amino acid protein displaying a conserved single active site and a putative C-terminal transmembrane anchor, thus resembling human tACE, as supported by molecular modelling. FRET activity assays and Maldi-TOF spectrometry indicated that CgACE is a functional dipeptidyl-carboxypeptidase which is active on Angiotensin I and sensitive to ACE inhibitors and chloride ion concentration. Immunocytochemistry revealed that, as its human counterpart, recombinant CgACE is synthesised as a transmembrane enzyme. RT-qPCR, in-situ hybridization and immunohistochemistry shed light on a tissue, and development stage, specific expression pattern for CgACE, which is increased in the gonad during spermatogenesis. The use of ACE inhibitors in vivo indicates that the dipeptidase activity of CgACE is crucial for the oyster fertilization. Our study demonstrates that a transmembrane active ACE is present in the oyster Crassostrea gigas, and for the first time ascribes a functional role for ACE in Lophotrochozoans. Its biological function in reproduction is conserved from molluscs to humans, a finding of particular evolutionary interest especially since oysters represent the most important aquaculture resource worldwide. Text Crassostrea gigas PubMed Central (PMC) PLoS ONE 6 12 e27833 |
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Research Article Riviere, Guillaume Fellous, Alexandre Franco, Alban Bernay, Benoit Favrel, Pascal A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE |
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Angiotensin-converting enzyme (ACE) is a highly conserved metallopeptidase. In mammals, the somatic isoform governs blood pressure whereas the germinal isoform (tACE) is required for fertility. In Ecdysozoans, ACE-like enzymes are implicated in reproduction. Despite ACE orthologues being present from bacteria to humans, their function(s) remain(s) unknown in distant organisms such as Lophotrochozoans. In silico analysis of an oyster (Crassostrea gigas) EST library suggested the presence of an ACE orthologue in molluscs. Primer walking and 5′-RACE revealed that the 1.9 kb cDNA encodes CgACE, a 632 amino acid protein displaying a conserved single active site and a putative C-terminal transmembrane anchor, thus resembling human tACE, as supported by molecular modelling. FRET activity assays and Maldi-TOF spectrometry indicated that CgACE is a functional dipeptidyl-carboxypeptidase which is active on Angiotensin I and sensitive to ACE inhibitors and chloride ion concentration. Immunocytochemistry revealed that, as its human counterpart, recombinant CgACE is synthesised as a transmembrane enzyme. RT-qPCR, in-situ hybridization and immunohistochemistry shed light on a tissue, and development stage, specific expression pattern for CgACE, which is increased in the gonad during spermatogenesis. The use of ACE inhibitors in vivo indicates that the dipeptidase activity of CgACE is crucial for the oyster fertilization. Our study demonstrates that a transmembrane active ACE is present in the oyster Crassostrea gigas, and for the first time ascribes a functional role for ACE in Lophotrochozoans. Its biological function in reproduction is conserved from molluscs to humans, a finding of particular evolutionary interest especially since oysters represent the most important aquaculture resource worldwide. |
format |
Text |
author |
Riviere, Guillaume Fellous, Alexandre Franco, Alban Bernay, Benoit Favrel, Pascal |
author_facet |
Riviere, Guillaume Fellous, Alexandre Franco, Alban Bernay, Benoit Favrel, Pascal |
author_sort |
Riviere, Guillaume |
title |
A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE |
title_short |
A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE |
title_full |
A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE |
title_fullStr |
A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE |
title_full_unstemmed |
A Crucial Role in Fertility for the Oyster Angiotensin-Converting Enzyme Orthologue CgACE |
title_sort |
crucial role in fertility for the oyster angiotensin-converting enzyme orthologue cgace |
publisher |
Public Library of Science |
publishDate |
2011 |
url |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235092 http://www.ncbi.nlm.nih.gov/pubmed/22174750 https://doi.org/10.1371/journal.pone.0027833 |
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Crassostrea gigas |
genre_facet |
Crassostrea gigas |
op_relation |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235092 http://www.ncbi.nlm.nih.gov/pubmed/22174750 http://dx.doi.org/10.1371/journal.pone.0027833 |
op_rights |
Riviere et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
op_rightsnorm |
CC-BY |
op_doi |
https://doi.org/10.1371/journal.pone.0027833 |
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PLoS ONE |
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12 |
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e27833 |
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