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Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight

Adamts16 encodes a disintegrin-like and metalloproteinase with thrombospondin motifs, 16, a member of a family of multi-domain, zinc-binding proteinases. ADAMTS-16 is implicated in a number of pathological conditions, including hypertension, cancer and osteoarthritis. A large number of observations,...

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Autores principales: Livermore, Catherine, Warr, Nick, Chalon, Nicolas, Siggers, Pam, Mianné, Joffrey, Codner, Gemma, Teboul, Lydia, Wells, Sara, Greenfield, Andy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868159/
https://www.ncbi.nlm.nih.gov/pubmed/31748609
http://dx.doi.org/10.1038/s41598-019-53900-0
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author Livermore, Catherine
Warr, Nick
Chalon, Nicolas
Siggers, Pam
Mianné, Joffrey
Codner, Gemma
Teboul, Lydia
Wells, Sara
Greenfield, Andy
author_facet Livermore, Catherine
Warr, Nick
Chalon, Nicolas
Siggers, Pam
Mianné, Joffrey
Codner, Gemma
Teboul, Lydia
Wells, Sara
Greenfield, Andy
author_sort Livermore, Catherine
collection PubMed
description Adamts16 encodes a disintegrin-like and metalloproteinase with thrombospondin motifs, 16, a member of a family of multi-domain, zinc-binding proteinases. ADAMTS-16 is implicated in a number of pathological conditions, including hypertension, cancer and osteoarthritis. A large number of observations, including a recent report of human ADAMTS16 variants in cases of 46,XY disorders/differences of sex development (DSD), also implicate this gene in human testis determination. We used CRISPR/Cas9 genome editing to generate a loss-of-function allele in the mouse in order to examine whether ADAMTS-16 functions in mouse testis determination or testicular function. Male mice lacking Adamts16 on the C57BL/6N background undergo normal testis determination in the fetal period. However, adult homozygotes have an average testis weight that is around 10% lower than age-matched controls. Cohorts of mutant males tested at 3-months and 6-months of age were fertile. We conclude that ADAMTS-16 is not required for testis determination or male fertility in mice. We discuss these phenotypic data and their significance for our understanding of ADAMTS-16 function.
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spelling pubmed-68681592019-12-04 Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight Livermore, Catherine Warr, Nick Chalon, Nicolas Siggers, Pam Mianné, Joffrey Codner, Gemma Teboul, Lydia Wells, Sara Greenfield, Andy Sci Rep Article Adamts16 encodes a disintegrin-like and metalloproteinase with thrombospondin motifs, 16, a member of a family of multi-domain, zinc-binding proteinases. ADAMTS-16 is implicated in a number of pathological conditions, including hypertension, cancer and osteoarthritis. A large number of observations, including a recent report of human ADAMTS16 variants in cases of 46,XY disorders/differences of sex development (DSD), also implicate this gene in human testis determination. We used CRISPR/Cas9 genome editing to generate a loss-of-function allele in the mouse in order to examine whether ADAMTS-16 functions in mouse testis determination or testicular function. Male mice lacking Adamts16 on the C57BL/6N background undergo normal testis determination in the fetal period. However, adult homozygotes have an average testis weight that is around 10% lower than age-matched controls. Cohorts of mutant males tested at 3-months and 6-months of age were fertile. We conclude that ADAMTS-16 is not required for testis determination or male fertility in mice. We discuss these phenotypic data and their significance for our understanding of ADAMTS-16 function. Nature Publishing Group UK 2019-11-20 /pmc/articles/PMC6868159/ /pubmed/31748609 http://dx.doi.org/10.1038/s41598-019-53900-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Livermore, Catherine
Warr, Nick
Chalon, Nicolas
Siggers, Pam
Mianné, Joffrey
Codner, Gemma
Teboul, Lydia
Wells, Sara
Greenfield, Andy
Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight
title Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight
title_full Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight
title_fullStr Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight
title_full_unstemmed Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight
title_short Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight
title_sort male mice lacking adamts-16 are fertile but exhibit testes of reduced weight
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868159/
https://www.ncbi.nlm.nih.gov/pubmed/31748609
http://dx.doi.org/10.1038/s41598-019-53900-0
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