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Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing

The mammalian epididymis is a highly specialized region of the male reproductive tract that is lined with a continuous layer of epithelial cells that display a remarkable level of regionalized secretory and absorptive activity. The luminal environment created by this combined secretory and absorptiv...

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Autores principales: Anderson, Amanda L., Stanger, Simone J., Mihalas, Bettina P., Tyagi, Sonika, Holt, Janet E., McLaughlin, Eileen A., Nixon, Brett
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664737/
https://www.ncbi.nlm.nih.gov/pubmed/26697376
http://dx.doi.org/10.1016/j.gdata.2015.09.012
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author Anderson, Amanda L.
Stanger, Simone J.
Mihalas, Bettina P.
Tyagi, Sonika
Holt, Janet E.
McLaughlin, Eileen A.
Nixon, Brett
author_facet Anderson, Amanda L.
Stanger, Simone J.
Mihalas, Bettina P.
Tyagi, Sonika
Holt, Janet E.
McLaughlin, Eileen A.
Nixon, Brett
author_sort Anderson, Amanda L.
collection PubMed
description The mammalian epididymis is a highly specialized region of the male reproductive tract that is lined with a continuous layer of epithelial cells that display a remarkable level of regionalized secretory and absorptive activity. The luminal environment created by this combined secretory and absorptive activity is directly responsible for promoting the functional maturation of spermatozoa and their maintenance in a quiescent and viable state prior to ejaculation. This study was designed to identify the complement of microRNAs (miRNAs) that are expressed within the mouse epididymal epithelial cells and the maturing populations of spermatozoa. Through the use of Next Generation Sequencing technology we have demonstrated that both epididymal epithelial cells and spermatozoa harbour a complex repertoire of miRNAs that have substantially different expression profiles along the length of the tract. These data, deposited in the Gene Expression Omnibus (GEO) with the accession numbers GSE70197 and GSE70198, afford valuable insight into the post-transcriptional control of gene expression within the epididymis and provide the first evidence for the dynamic transformation of the miRNA content of maturing sperm cells. Ultimately such information promises to inform our understanding of the aetiology of male infertility. Herein we provide a detailed description of the methodology used to generate these important data.
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spelling pubmed-46647372015-12-22 Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing Anderson, Amanda L. Stanger, Simone J. Mihalas, Bettina P. Tyagi, Sonika Holt, Janet E. McLaughlin, Eileen A. Nixon, Brett Genom Data Data in Brief The mammalian epididymis is a highly specialized region of the male reproductive tract that is lined with a continuous layer of epithelial cells that display a remarkable level of regionalized secretory and absorptive activity. The luminal environment created by this combined secretory and absorptive activity is directly responsible for promoting the functional maturation of spermatozoa and their maintenance in a quiescent and viable state prior to ejaculation. This study was designed to identify the complement of microRNAs (miRNAs) that are expressed within the mouse epididymal epithelial cells and the maturing populations of spermatozoa. Through the use of Next Generation Sequencing technology we have demonstrated that both epididymal epithelial cells and spermatozoa harbour a complex repertoire of miRNAs that have substantially different expression profiles along the length of the tract. These data, deposited in the Gene Expression Omnibus (GEO) with the accession numbers GSE70197 and GSE70198, afford valuable insight into the post-transcriptional control of gene expression within the epididymis and provide the first evidence for the dynamic transformation of the miRNA content of maturing sperm cells. Ultimately such information promises to inform our understanding of the aetiology of male infertility. Herein we provide a detailed description of the methodology used to generate these important data. Elsevier 2015-09-18 /pmc/articles/PMC4664737/ /pubmed/26697376 http://dx.doi.org/10.1016/j.gdata.2015.09.012 Text en © 2015 Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Data in Brief
Anderson, Amanda L.
Stanger, Simone J.
Mihalas, Bettina P.
Tyagi, Sonika
Holt, Janet E.
McLaughlin, Eileen A.
Nixon, Brett
Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
title Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
title_full Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
title_fullStr Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
title_full_unstemmed Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
title_short Assessment of microRNA expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
title_sort assessment of microrna expression in mouse epididymal epithelial cells and spermatozoa by next generation sequencing
topic Data in Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664737/
https://www.ncbi.nlm.nih.gov/pubmed/26697376
http://dx.doi.org/10.1016/j.gdata.2015.09.012
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