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Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals

BACKGROUND: Mammals have wide variations in testicular position, with scrotal testes in some species and ascrotal testes in others. Although cryptorchidism is hazardous to human health, some mammalian taxa are natural cryptorchids. However, the evolution of testicular position and the molecular mech...

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Autores principales: Chai, Simin, Huang, Xin, Wu, Tianzhen, Xu, Shixia, Ren, Wenhua, Yang, Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547080/
https://www.ncbi.nlm.nih.gov/pubmed/34702182
http://dx.doi.org/10.1186/s12864-021-08084-1
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author Chai, Simin
Huang, Xin
Wu, Tianzhen
Xu, Shixia
Ren, Wenhua
Yang, Guang
author_facet Chai, Simin
Huang, Xin
Wu, Tianzhen
Xu, Shixia
Ren, Wenhua
Yang, Guang
author_sort Chai, Simin
collection PubMed
description BACKGROUND: Mammals have wide variations in testicular position, with scrotal testes in some species and ascrotal testes in others. Although cryptorchidism is hazardous to human health, some mammalian taxa are natural cryptorchids. However, the evolution of testicular position and the molecular mechanisms underlying the maintenance of health, including reproductive health, in ascrotal mammals are not clear. RESULTS: In the present study, comparative genomics and evolutionary analyses revealed that genes associated with the extracellular matrix and muscle, contributing to the development of the gubernaculum, were involved in the evolution of testicular position in mammals. Moreover, genes related to testicular position were significantly associated with spermatogenesis and sperm fertility. These genes showed rapid evolution and the signature of positive selection, with specific substitutions in ascrotal mammals. Genes associated with testicular position were significantly enriched in functions and pathways related to cancer, DNA repair, DNA replication, and autophagy. CONCLUSIONS: Our results revealed that alterations in gubernaculum development contributed to the evolution of testicular position in mammals and provided the first support for two hypotheses for variation in testicular position in mammals, the “cooling hypothesis”, which proposes that the scrotum provides a cool environment for acutely heat-sensitive sperm and the “training hypothesis”, which proposes that the scrotum develops the sperm by exposing them to an exterior environment. Further, we identified cancer resistance and DNA repair as potential protective mechanisms in natural cryptorchids. These findings provide general insights into cryptorchidism and have implications for health and infertility both in humans and domestic mammals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08084-1.
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spelling pubmed-85470802021-10-26 Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals Chai, Simin Huang, Xin Wu, Tianzhen Xu, Shixia Ren, Wenhua Yang, Guang BMC Genomics Research BACKGROUND: Mammals have wide variations in testicular position, with scrotal testes in some species and ascrotal testes in others. Although cryptorchidism is hazardous to human health, some mammalian taxa are natural cryptorchids. However, the evolution of testicular position and the molecular mechanisms underlying the maintenance of health, including reproductive health, in ascrotal mammals are not clear. RESULTS: In the present study, comparative genomics and evolutionary analyses revealed that genes associated with the extracellular matrix and muscle, contributing to the development of the gubernaculum, were involved in the evolution of testicular position in mammals. Moreover, genes related to testicular position were significantly associated with spermatogenesis and sperm fertility. These genes showed rapid evolution and the signature of positive selection, with specific substitutions in ascrotal mammals. Genes associated with testicular position were significantly enriched in functions and pathways related to cancer, DNA repair, DNA replication, and autophagy. CONCLUSIONS: Our results revealed that alterations in gubernaculum development contributed to the evolution of testicular position in mammals and provided the first support for two hypotheses for variation in testicular position in mammals, the “cooling hypothesis”, which proposes that the scrotum provides a cool environment for acutely heat-sensitive sperm and the “training hypothesis”, which proposes that the scrotum develops the sperm by exposing them to an exterior environment. Further, we identified cancer resistance and DNA repair as potential protective mechanisms in natural cryptorchids. These findings provide general insights into cryptorchidism and have implications for health and infertility both in humans and domestic mammals. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08084-1. BioMed Central 2021-10-26 /pmc/articles/PMC8547080/ /pubmed/34702182 http://dx.doi.org/10.1186/s12864-021-08084-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chai, Simin
Huang, Xin
Wu, Tianzhen
Xu, Shixia
Ren, Wenhua
Yang, Guang
Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
title Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
title_full Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
title_fullStr Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
title_full_unstemmed Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
title_short Comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
title_sort comparative genomics reveals molecular mechanisms underlying health and reproduction in cryptorchid mammals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547080/
https://www.ncbi.nlm.nih.gov/pubmed/34702182
http://dx.doi.org/10.1186/s12864-021-08084-1
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