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Global methylation status of sperm DNA in carriers of chromosome structural aberrations

Male infertility might be clearly associated with aberrant DNA methylation patterns in human spermatozoa. An association between oxidative stress and the global methylation status of the sperm genome has also been suggested. The aim of the present study was to determine whether the global sperm DNA...

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Autores principales: Olszewska, Marta, Barciszewska, Miroslawa Z, Fraczek, Monika, Huleyuk, Nataliya, Chernykh, Vyacheslav B, Zastavna, Danuta, Barciszewski, Jan, Kurpisz, Maciej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227660/
https://www.ncbi.nlm.nih.gov/pubmed/26908061
http://dx.doi.org/10.4103/1008-682X.168684
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author Olszewska, Marta
Barciszewska, Miroslawa Z
Fraczek, Monika
Huleyuk, Nataliya
Chernykh, Vyacheslav B
Zastavna, Danuta
Barciszewski, Jan
Kurpisz, Maciej
author_facet Olszewska, Marta
Barciszewska, Miroslawa Z
Fraczek, Monika
Huleyuk, Nataliya
Chernykh, Vyacheslav B
Zastavna, Danuta
Barciszewski, Jan
Kurpisz, Maciej
author_sort Olszewska, Marta
collection PubMed
description Male infertility might be clearly associated with aberrant DNA methylation patterns in human spermatozoa. An association between oxidative stress and the global methylation status of the sperm genome has also been suggested. The aim of the present study was to determine whether the global sperm DNA methylation status was affected in the spermatozoa of carriers of chromosome structural aberrations. The relationships between the 5-methylcytosine (m(5)C) levels in spermatozoa and chromatin integrity status were evaluated. The study patients comprised male carriers of chromosome structural aberrations with reproductive failure (n = 24), and the controls comprised normozoospermic sperm volunteers (n = 23). The global m(5)C level was measured using thin-layer chromatography (TLC) and immunofluorescence (IF) techniques. The sperm chromatin integrity was assessed using aniline blue (AB) staining and TUNEL assay. The mean m(5)C levels were similar between the investigated chromosome structural aberrations carriers (P) and controls (K). However, sperm chromatin integrity tests revealed significantly higher values in chromosomal rearrangement carriers than in controls (P < 0.05). Although the potential relationship between sperm chromatin integrity status and sperm DNA fragmentation and the m(5)C level juxtaposed in both analyzed groups (P vs K) was represented in a clearly opposite manner, the low chromatin integrity might be associated with the high hypomethylation status of the sperm DNA observed in carriers of chromosome structural aberrations.
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spelling pubmed-52276602017-02-03 Global methylation status of sperm DNA in carriers of chromosome structural aberrations Olszewska, Marta Barciszewska, Miroslawa Z Fraczek, Monika Huleyuk, Nataliya Chernykh, Vyacheslav B Zastavna, Danuta Barciszewski, Jan Kurpisz, Maciej Asian J Androl Original Article Male infertility might be clearly associated with aberrant DNA methylation patterns in human spermatozoa. An association between oxidative stress and the global methylation status of the sperm genome has also been suggested. The aim of the present study was to determine whether the global sperm DNA methylation status was affected in the spermatozoa of carriers of chromosome structural aberrations. The relationships between the 5-methylcytosine (m(5)C) levels in spermatozoa and chromatin integrity status were evaluated. The study patients comprised male carriers of chromosome structural aberrations with reproductive failure (n = 24), and the controls comprised normozoospermic sperm volunteers (n = 23). The global m(5)C level was measured using thin-layer chromatography (TLC) and immunofluorescence (IF) techniques. The sperm chromatin integrity was assessed using aniline blue (AB) staining and TUNEL assay. The mean m(5)C levels were similar between the investigated chromosome structural aberrations carriers (P) and controls (K). However, sperm chromatin integrity tests revealed significantly higher values in chromosomal rearrangement carriers than in controls (P < 0.05). Although the potential relationship between sperm chromatin integrity status and sperm DNA fragmentation and the m(5)C level juxtaposed in both analyzed groups (P vs K) was represented in a clearly opposite manner, the low chromatin integrity might be associated with the high hypomethylation status of the sperm DNA observed in carriers of chromosome structural aberrations. Medknow Publications & Media Pvt Ltd 2017 2016-02-19 /pmc/articles/PMC5227660/ /pubmed/26908061 http://dx.doi.org/10.4103/1008-682X.168684 Text en Copyright: © 2017 AJA, SIMM & SJTU http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Olszewska, Marta
Barciszewska, Miroslawa Z
Fraczek, Monika
Huleyuk, Nataliya
Chernykh, Vyacheslav B
Zastavna, Danuta
Barciszewski, Jan
Kurpisz, Maciej
Global methylation status of sperm DNA in carriers of chromosome structural aberrations
title Global methylation status of sperm DNA in carriers of chromosome structural aberrations
title_full Global methylation status of sperm DNA in carriers of chromosome structural aberrations
title_fullStr Global methylation status of sperm DNA in carriers of chromosome structural aberrations
title_full_unstemmed Global methylation status of sperm DNA in carriers of chromosome structural aberrations
title_short Global methylation status of sperm DNA in carriers of chromosome structural aberrations
title_sort global methylation status of sperm dna in carriers of chromosome structural aberrations
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227660/
https://www.ncbi.nlm.nih.gov/pubmed/26908061
http://dx.doi.org/10.4103/1008-682X.168684
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