Cargando…
Epigenetics, cryptorchidism, and infertility
BACKGROUND: Cryptorchid boys with defective mini-puberty and impaired differentiation of Ad spermatogonia (high infertility risk) have altered expression of several genes encoding histone methyltransferases compared to patients with intact differentiation of gonocytes into Ad spermatogonia (low infe...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512650/ https://www.ncbi.nlm.nih.gov/pubmed/37730534 http://dx.doi.org/10.1186/s12610-023-00199-7 |
_version_ | 1785108408597217280 |
---|---|
author | Hadziselimovic, Faruk Verkauskas, Gilvydas Stadler, Michael B. |
author_facet | Hadziselimovic, Faruk Verkauskas, Gilvydas Stadler, Michael B. |
author_sort | Hadziselimovic, Faruk |
collection | PubMed |
description | BACKGROUND: Cryptorchid boys with defective mini-puberty and impaired differentiation of Ad spermatogonia (high infertility risk) have altered expression of several genes encoding histone methyltransferases compared to patients with intact differentiation of gonocytes into Ad spermatogonia (low infertility risk). RESULTS: High infertility risk cryptorchid boys display hypogonadotropic hypogonadism, which, together with the diminished expression of histone deacetylases and increased expression of HDAC8 decrotonylase, indicates altered histone marks and, thus, a perturbed histone code. Curative GnRHa treatment induces normalization of histone methyltransferase, chromatin remodeling, and histone deacetylase gene expression. As a result, histone changes induce differentiation of Ad spermatogonia from their precursors and, thus, fertility. In this short report, we describe key functions of histone lysine methyltransferases, chromatin remodeling proteins, and long-noncoding RNAs, and discuss their potential roles in processes leading to infertility. CONCLUSION: Our findings suggest that epigenetic mechanisms are critical to better understanding the root causes underlying male infertility related to cryptorchidism and its possible transgenerational transmission. |
format | Online Article Text |
id | pubmed-10512650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105126502023-09-22 Epigenetics, cryptorchidism, and infertility Hadziselimovic, Faruk Verkauskas, Gilvydas Stadler, Michael B. Basic Clin Androl Short Report BACKGROUND: Cryptorchid boys with defective mini-puberty and impaired differentiation of Ad spermatogonia (high infertility risk) have altered expression of several genes encoding histone methyltransferases compared to patients with intact differentiation of gonocytes into Ad spermatogonia (low infertility risk). RESULTS: High infertility risk cryptorchid boys display hypogonadotropic hypogonadism, which, together with the diminished expression of histone deacetylases and increased expression of HDAC8 decrotonylase, indicates altered histone marks and, thus, a perturbed histone code. Curative GnRHa treatment induces normalization of histone methyltransferase, chromatin remodeling, and histone deacetylase gene expression. As a result, histone changes induce differentiation of Ad spermatogonia from their precursors and, thus, fertility. In this short report, we describe key functions of histone lysine methyltransferases, chromatin remodeling proteins, and long-noncoding RNAs, and discuss their potential roles in processes leading to infertility. CONCLUSION: Our findings suggest that epigenetic mechanisms are critical to better understanding the root causes underlying male infertility related to cryptorchidism and its possible transgenerational transmission. BioMed Central 2023-09-21 /pmc/articles/PMC10512650/ /pubmed/37730534 http://dx.doi.org/10.1186/s12610-023-00199-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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 | Short Report Hadziselimovic, Faruk Verkauskas, Gilvydas Stadler, Michael B. Epigenetics, cryptorchidism, and infertility |
title | Epigenetics, cryptorchidism, and infertility |
title_full | Epigenetics, cryptorchidism, and infertility |
title_fullStr | Epigenetics, cryptorchidism, and infertility |
title_full_unstemmed | Epigenetics, cryptorchidism, and infertility |
title_short | Epigenetics, cryptorchidism, and infertility |
title_sort | epigenetics, cryptorchidism, and infertility |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512650/ https://www.ncbi.nlm.nih.gov/pubmed/37730534 http://dx.doi.org/10.1186/s12610-023-00199-7 |
work_keys_str_mv | AT hadziselimovicfaruk epigeneticscryptorchidismandinfertility AT verkauskasgilvydas epigeneticscryptorchidismandinfertility AT stadlermichaelb epigeneticscryptorchidismandinfertility |