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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,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6868159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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