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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...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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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. |
format | Text |
id | pubmed-2655651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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