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Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input

We developed a simplified workflow of gDNA extraction from ejaculated bovine sperm using a low total number of sperm and a short time frame that yields high-quality DNA suitable for downstream methylation and genome analyses. These techniques have broad implications in human biomedical sciences and...

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Detalles Bibliográficos
Autores principales: Daigneault, Bradford W, Rajput, Sandeep K, Smith, George W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092705/
https://www.ncbi.nlm.nih.gov/pubmed/31937114
http://dx.doi.org/10.2144/btn-2019-0121
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author Daigneault, Bradford W
Rajput, Sandeep K
Smith, George W
author_facet Daigneault, Bradford W
Rajput, Sandeep K
Smith, George W
author_sort Daigneault, Bradford W
collection PubMed
description We developed a simplified workflow of gDNA extraction from ejaculated bovine sperm using a low total number of sperm and a short time frame that yields high-quality DNA suitable for downstream methylation and genome analyses. These techniques have broad implications in human biomedical sciences and agriculture, including clinical diagnoses of infertility, the identification of single-nucleotide polymorphisms and aberrant methylation patterns that can impact fertility, lower embryo development and contribute to heritable disease. The methods described here provide a reliable, simplistic approach for analyzing both the genomic and epigenomic status of whole sperm ejaculates that can be adapted for laboratory diagnostics, clinical reproductive practice and basic research.
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spelling pubmed-70927052020-03-24 Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input Daigneault, Bradford W Rajput, Sandeep K Smith, George W Biotechniques Benchmark We developed a simplified workflow of gDNA extraction from ejaculated bovine sperm using a low total number of sperm and a short time frame that yields high-quality DNA suitable for downstream methylation and genome analyses. These techniques have broad implications in human biomedical sciences and agriculture, including clinical diagnoses of infertility, the identification of single-nucleotide polymorphisms and aberrant methylation patterns that can impact fertility, lower embryo development and contribute to heritable disease. The methods described here provide a reliable, simplistic approach for analyzing both the genomic and epigenomic status of whole sperm ejaculates that can be adapted for laboratory diagnostics, clinical reproductive practice and basic research. Future Science Ltd 2020-01-16 2019-12 /pmc/articles/PMC7092705/ /pubmed/31937114 http://dx.doi.org/10.2144/btn-2019-0121 Text en © 2020 Bradford W. Daigneault This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Benchmark
Daigneault, Bradford W
Rajput, Sandeep K
Smith, George W
Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
title Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
title_full Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
title_fullStr Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
title_full_unstemmed Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
title_short Simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
title_sort simple workflow for genome and methylation analyses of ejaculated bovine spermatozoa with low sperm input
topic Benchmark
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7092705/
https://www.ncbi.nlm.nih.gov/pubmed/31937114
http://dx.doi.org/10.2144/btn-2019-0121
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