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The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes
At the end of mammalian sperm development, sperm cells expel most of their cytoplasm and dispose of the majority of their RNA. Yet, hundreds of RNA molecules remain in mature sperm. The biological significance of the vast majority of these molecules is unclear. To better understand the processes tha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436662/ https://www.ncbi.nlm.nih.gov/pubmed/25904136 http://dx.doi.org/10.1261/rna.046482.114 |
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author | Pantano, Lorena Jodar, Meritxell Bak, Mads Ballescà, Josep Lluís Tommerup, Niels Oliva, Rafael Vavouri, Tanya |
author_facet | Pantano, Lorena Jodar, Meritxell Bak, Mads Ballescà, Josep Lluís Tommerup, Niels Oliva, Rafael Vavouri, Tanya |
author_sort | Pantano, Lorena |
collection | PubMed |
description | At the end of mammalian sperm development, sperm cells expel most of their cytoplasm and dispose of the majority of their RNA. Yet, hundreds of RNA molecules remain in mature sperm. The biological significance of the vast majority of these molecules is unclear. To better understand the processes that generate sperm small RNAs and what roles they may have, we sequenced and characterized the small RNA content of sperm samples from two human fertile individuals. We detected 182 microRNAs, some of which are highly abundant. The most abundant microRNA in sperm is miR-1246 with predicted targets among sperm-specific genes. The most abundant class of small noncoding RNAs in sperm are PIWI-interacting RNAs (piRNAs). Surprisingly, we found that human sperm cells contain piRNAs processed from pseudogenes. Clusters of piRNAs from human testes contain pseudogenes transcribed in the antisense strand and processed into small RNAs. Several human protein-coding genes contain antisense predicted targets of pseudogene-derived piRNAs in the male germline and these piRNAs are still found in mature sperm. Our study provides the most extensive data set and annotation of human sperm small RNAs to date and is a resource for further functional studies on the roles of sperm small RNAs. In addition, we propose that some of the pseudogene-derived human piRNAs may regulate expression of their parent gene in the male germline. |
format | Online Article Text |
id | pubmed-4436662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44366622016-06-01 The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes Pantano, Lorena Jodar, Meritxell Bak, Mads Ballescà, Josep Lluís Tommerup, Niels Oliva, Rafael Vavouri, Tanya RNA Bioinformatics At the end of mammalian sperm development, sperm cells expel most of their cytoplasm and dispose of the majority of their RNA. Yet, hundreds of RNA molecules remain in mature sperm. The biological significance of the vast majority of these molecules is unclear. To better understand the processes that generate sperm small RNAs and what roles they may have, we sequenced and characterized the small RNA content of sperm samples from two human fertile individuals. We detected 182 microRNAs, some of which are highly abundant. The most abundant microRNA in sperm is miR-1246 with predicted targets among sperm-specific genes. The most abundant class of small noncoding RNAs in sperm are PIWI-interacting RNAs (piRNAs). Surprisingly, we found that human sperm cells contain piRNAs processed from pseudogenes. Clusters of piRNAs from human testes contain pseudogenes transcribed in the antisense strand and processed into small RNAs. Several human protein-coding genes contain antisense predicted targets of pseudogene-derived piRNAs in the male germline and these piRNAs are still found in mature sperm. Our study provides the most extensive data set and annotation of human sperm small RNAs to date and is a resource for further functional studies on the roles of sperm small RNAs. In addition, we propose that some of the pseudogene-derived human piRNAs may regulate expression of their parent gene in the male germline. Cold Spring Harbor Laboratory Press 2015-06 /pmc/articles/PMC4436662/ /pubmed/25904136 http://dx.doi.org/10.1261/rna.046482.114 Text en © 2015 Pantano et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Bioinformatics Pantano, Lorena Jodar, Meritxell Bak, Mads Ballescà, Josep Lluís Tommerup, Niels Oliva, Rafael Vavouri, Tanya The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
title | The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
title_full | The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
title_fullStr | The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
title_full_unstemmed | The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
title_short | The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
title_sort | small rna content of human sperm reveals pseudogene-derived pirnas complementary to protein-coding genes |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436662/ https://www.ncbi.nlm.nih.gov/pubmed/25904136 http://dx.doi.org/10.1261/rna.046482.114 |
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