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Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction

Hydrocephalus with hop gait (hyh) is a recessive inheritable disease that arose spontaneously in a mouse strain. A missense mutation in the Napa gene that results in the substitution of a methionine for isoleucine at position 105 (M105I) of αSNAP has been detected in these animals. αSNAP is a ubiqui...

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Autores principales: Bátiz, Luis Federico, De Blas, Gerardo A., Michaut, Marcela A., Ramírez, Alfredo R., Rodríguez, Facundo, Ratto, Marcelo H., Oliver, Cristian, Tomes, Claudia N., Rodríguez, Esteban M., Mayorga, Luis S.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2655651/
https://www.ncbi.nlm.nih.gov/pubmed/19305511
http://dx.doi.org/10.1371/journal.pone.0004963
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author Bátiz, Luis Federico
De Blas, Gerardo A.
Michaut, Marcela A.
Ramírez, Alfredo R.
Rodríguez, Facundo
Ratto, Marcelo H.
Oliver, Cristian
Tomes, Claudia N.
Rodríguez, Esteban M.
Mayorga, Luis S.
author_facet Bátiz, Luis Federico
De Blas, Gerardo A.
Michaut, Marcela A.
Ramírez, Alfredo R.
Rodríguez, Facundo
Ratto, Marcelo H.
Oliver, Cristian
Tomes, Claudia N.
Rodríguez, Esteban M.
Mayorga, Luis S.
author_sort Bátiz, Luis Federico
collection PubMed
description Hydrocephalus with hop gait (hyh) is a recessive inheritable disease that arose spontaneously in a mouse strain. A missense mutation in the Napa gene that results in the substitution of a methionine for isoleucine at position 105 (M105I) of αSNAP has been detected in these animals. αSNAP is a ubiquitous protein that plays a key role in membrane fusion and exocytosis. In this study, we found that male hyh mice with a mild phenotype produced morphologically normal and motile sperm, but had a strongly reduced fertility. When stimulated with progesterone or A23187 (a calcium ionophore), sperm from these animals had a defective acrosome reaction. It has been reported that the M105I mutation affects the expression but not the function of the protein. Consistent with an hypomorphic phenotype, the testes and epididymides of hyh mice had low amounts of the mutated protein. In contrast, sperm had αSNAP levels indistinguishable from those found in wild type cells, suggesting that the mutated protein is not fully functional for acrosomal exocytosis. Corroborating this possibility, addition of recombinant wild type αSNAP rescued exocytosis in streptolysin O-permeabilized sperm, while the mutant protein was ineffective. Moreover, addition of recombinant αSNAP. M105I inhibited acrosomal exocytosis in permeabilized human and wild type mouse sperm. We conclude that the M105I mutation affects the expression and also the function of αSNAP, and that a fully functional αSNAP is necessary for acrosomal exocytosis, a key event in fertilization.
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spelling pubmed-26556512009-03-23 Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction Bátiz, Luis Federico De Blas, Gerardo A. Michaut, Marcela A. Ramírez, Alfredo R. Rodríguez, Facundo Ratto, Marcelo H. Oliver, Cristian Tomes, Claudia N. Rodríguez, Esteban M. Mayorga, Luis S. PLoS One Research Article Hydrocephalus with hop gait (hyh) is a recessive inheritable disease that arose spontaneously in a mouse strain. A missense mutation in the Napa gene that results in the substitution of a methionine for isoleucine at position 105 (M105I) of αSNAP has been detected in these animals. αSNAP is a ubiquitous protein that plays a key role in membrane fusion and exocytosis. In this study, we found that male hyh mice with a mild phenotype produced morphologically normal and motile sperm, but had a strongly reduced fertility. When stimulated with progesterone or A23187 (a calcium ionophore), sperm from these animals had a defective acrosome reaction. It has been reported that the M105I mutation affects the expression but not the function of the protein. Consistent with an hypomorphic phenotype, the testes and epididymides of hyh mice had low amounts of the mutated protein. In contrast, sperm had αSNAP levels indistinguishable from those found in wild type cells, suggesting that the mutated protein is not fully functional for acrosomal exocytosis. Corroborating this possibility, addition of recombinant wild type αSNAP rescued exocytosis in streptolysin O-permeabilized sperm, while the mutant protein was ineffective. Moreover, addition of recombinant αSNAP. M105I inhibited acrosomal exocytosis in permeabilized human and wild type mouse sperm. We conclude that the M105I mutation affects the expression and also the function of αSNAP, and that a fully functional αSNAP is necessary for acrosomal exocytosis, a key event in fertilization. Public Library of Science 2009-03-23 /pmc/articles/PMC2655651/ /pubmed/19305511 http://dx.doi.org/10.1371/journal.pone.0004963 Text en Bátiz et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Bátiz, Luis Federico
De Blas, Gerardo A.
Michaut, Marcela A.
Ramírez, Alfredo R.
Rodríguez, Facundo
Ratto, Marcelo H.
Oliver, Cristian
Tomes, Claudia N.
Rodríguez, Esteban M.
Mayorga, Luis S.
Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction
title Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction
title_full Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction
title_fullStr Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction
title_full_unstemmed Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction
title_short Sperm from Hyh Mice Carrying a Point Mutation in αSNAP Have a Defect in Acrosome Reaction
title_sort sperm from hyh mice carrying a point mutation in αsnap have a defect in acrosome reaction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2655651/
https://www.ncbi.nlm.nih.gov/pubmed/19305511
http://dx.doi.org/10.1371/journal.pone.0004963
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