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Sex-Biased Expression of MicroRNAs in Schistosoma mansoni

Schistosomiasis is an important neglected tropical disease caused by digenean helminth parasites of the genus Schistosoma. Schistosomes are unusual in that they are dioecious and the adult worms live in the blood system. MicroRNAs play crucial roles during gene regulation and are likely to be import...

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Detalles Bibliográficos
Autores principales: Marco, Antonio, Kozomara, Ana, Hui, Jerome H. L., Emery, Aidan M., Rollinson, David, Griffiths-Jones, Sam, Ronshaugen, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772069/
https://www.ncbi.nlm.nih.gov/pubmed/24069470
http://dx.doi.org/10.1371/journal.pntd.0002402
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author Marco, Antonio
Kozomara, Ana
Hui, Jerome H. L.
Emery, Aidan M.
Rollinson, David
Griffiths-Jones, Sam
Ronshaugen, Matthew
author_facet Marco, Antonio
Kozomara, Ana
Hui, Jerome H. L.
Emery, Aidan M.
Rollinson, David
Griffiths-Jones, Sam
Ronshaugen, Matthew
author_sort Marco, Antonio
collection PubMed
description Schistosomiasis is an important neglected tropical disease caused by digenean helminth parasites of the genus Schistosoma. Schistosomes are unusual in that they are dioecious and the adult worms live in the blood system. MicroRNAs play crucial roles during gene regulation and are likely to be important in sex differentiation in dioecious species. Here we characterize 112 microRNAs from adult Schistosoma mansoni individuals, including 84 novel microRNA families, and investigate the expression pattern in different sexes. By deep sequencing, we measured the relative expression levels of conserved and newly identified microRNAs between male and female samples. We observed that 13 microRNAs exhibited sex-biased expression, 10 of which are more abundant in females than in males. Sex chromosomes showed a paucity of female-biased genes, as predicted by theoretical evolutionary models. We propose that the recent emergence of separate sexes in Schistosoma had an effect on the chromosomal distribution and evolution of microRNAs, and that microRNAs are likely to participate in the sex differentiation/maintenance process.
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spelling pubmed-37720692013-09-25 Sex-Biased Expression of MicroRNAs in Schistosoma mansoni Marco, Antonio Kozomara, Ana Hui, Jerome H. L. Emery, Aidan M. Rollinson, David Griffiths-Jones, Sam Ronshaugen, Matthew PLoS Negl Trop Dis Research Article Schistosomiasis is an important neglected tropical disease caused by digenean helminth parasites of the genus Schistosoma. Schistosomes are unusual in that they are dioecious and the adult worms live in the blood system. MicroRNAs play crucial roles during gene regulation and are likely to be important in sex differentiation in dioecious species. Here we characterize 112 microRNAs from adult Schistosoma mansoni individuals, including 84 novel microRNA families, and investigate the expression pattern in different sexes. By deep sequencing, we measured the relative expression levels of conserved and newly identified microRNAs between male and female samples. We observed that 13 microRNAs exhibited sex-biased expression, 10 of which are more abundant in females than in males. Sex chromosomes showed a paucity of female-biased genes, as predicted by theoretical evolutionary models. We propose that the recent emergence of separate sexes in Schistosoma had an effect on the chromosomal distribution and evolution of microRNAs, and that microRNAs are likely to participate in the sex differentiation/maintenance process. Public Library of Science 2013-09-12 /pmc/articles/PMC3772069/ /pubmed/24069470 http://dx.doi.org/10.1371/journal.pntd.0002402 Text en © 2013 Marco et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Marco, Antonio
Kozomara, Ana
Hui, Jerome H. L.
Emery, Aidan M.
Rollinson, David
Griffiths-Jones, Sam
Ronshaugen, Matthew
Sex-Biased Expression of MicroRNAs in Schistosoma mansoni
title Sex-Biased Expression of MicroRNAs in Schistosoma mansoni
title_full Sex-Biased Expression of MicroRNAs in Schistosoma mansoni
title_fullStr Sex-Biased Expression of MicroRNAs in Schistosoma mansoni
title_full_unstemmed Sex-Biased Expression of MicroRNAs in Schistosoma mansoni
title_short Sex-Biased Expression of MicroRNAs in Schistosoma mansoni
title_sort sex-biased expression of micrornas in schistosoma mansoni
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772069/
https://www.ncbi.nlm.nih.gov/pubmed/24069470
http://dx.doi.org/10.1371/journal.pntd.0002402
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