Cargando…

Dynamic evolution and biogenesis of small RNAs during sex reversal

Understanding origin, evolution and functions of small RNA (sRNA) genes has been a great challenge in the past decade. Molecular mechanisms underlying sexual reversal in vertebrates, particularly sRNAs involved in this process, are largely unknown. By deep-sequencing of small RNA transcriptomes in c...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Jie, Luo, Majing, Sheng, Yue, Hong, Qiang, Cheng, Hanhua, Zhou, Rongjia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421800/
https://www.ncbi.nlm.nih.gov/pubmed/25944477
http://dx.doi.org/10.1038/srep09999
_version_ 1782369949304487936
author Liu, Jie
Luo, Majing
Sheng, Yue
Hong, Qiang
Cheng, Hanhua
Zhou, Rongjia
author_facet Liu, Jie
Luo, Majing
Sheng, Yue
Hong, Qiang
Cheng, Hanhua
Zhou, Rongjia
author_sort Liu, Jie
collection PubMed
description Understanding origin, evolution and functions of small RNA (sRNA) genes has been a great challenge in the past decade. Molecular mechanisms underlying sexual reversal in vertebrates, particularly sRNAs involved in this process, are largely unknown. By deep-sequencing of small RNA transcriptomes in combination with genomic analysis, we identified a large amount of piRNAs and miRNAs including over 1,000 novel miRNAs, which were differentially expressed during gonad reversal from ovary to testis via ovotesis. Biogenesis and expressions of miRNAs were dynamically changed during the reversal. Notably, phylogenetic analysis revealed dynamic expansions of miRNAs in vertebrates and an evolutionary trajectory of conserved miR-17-92 cluster in the Eukarya. We showed that the miR-17-92 cluster in vertebrates was generated through multiple duplications from ancestor miR-92 in invertebrates Tetranychus urticae and Daphnia pulex from the Chelicerata around 580 Mya. Moreover, we identified the sexual regulator Dmrt1 as a direct target of the members miR-19a and -19b in the cluster. These data suggested dynamic biogenesis and expressions of small RNAs during sex reversal and revealed multiple expansions and evolutionary trajectory of miRNAs from invertebrates to vertebrates, which implicate small RNAs in sexual reversal and provide new insight into evolutionary and molecular mechanisms underlying sexual reversal.
format Online
Article
Text
id pubmed-4421800
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-44218002015-05-18 Dynamic evolution and biogenesis of small RNAs during sex reversal Liu, Jie Luo, Majing Sheng, Yue Hong, Qiang Cheng, Hanhua Zhou, Rongjia Sci Rep Article Understanding origin, evolution and functions of small RNA (sRNA) genes has been a great challenge in the past decade. Molecular mechanisms underlying sexual reversal in vertebrates, particularly sRNAs involved in this process, are largely unknown. By deep-sequencing of small RNA transcriptomes in combination with genomic analysis, we identified a large amount of piRNAs and miRNAs including over 1,000 novel miRNAs, which were differentially expressed during gonad reversal from ovary to testis via ovotesis. Biogenesis and expressions of miRNAs were dynamically changed during the reversal. Notably, phylogenetic analysis revealed dynamic expansions of miRNAs in vertebrates and an evolutionary trajectory of conserved miR-17-92 cluster in the Eukarya. We showed that the miR-17-92 cluster in vertebrates was generated through multiple duplications from ancestor miR-92 in invertebrates Tetranychus urticae and Daphnia pulex from the Chelicerata around 580 Mya. Moreover, we identified the sexual regulator Dmrt1 as a direct target of the members miR-19a and -19b in the cluster. These data suggested dynamic biogenesis and expressions of small RNAs during sex reversal and revealed multiple expansions and evolutionary trajectory of miRNAs from invertebrates to vertebrates, which implicate small RNAs in sexual reversal and provide new insight into evolutionary and molecular mechanisms underlying sexual reversal. Nature Publishing Group 2015-05-06 /pmc/articles/PMC4421800/ /pubmed/25944477 http://dx.doi.org/10.1038/srep09999 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Liu, Jie
Luo, Majing
Sheng, Yue
Hong, Qiang
Cheng, Hanhua
Zhou, Rongjia
Dynamic evolution and biogenesis of small RNAs during sex reversal
title Dynamic evolution and biogenesis of small RNAs during sex reversal
title_full Dynamic evolution and biogenesis of small RNAs during sex reversal
title_fullStr Dynamic evolution and biogenesis of small RNAs during sex reversal
title_full_unstemmed Dynamic evolution and biogenesis of small RNAs during sex reversal
title_short Dynamic evolution and biogenesis of small RNAs during sex reversal
title_sort dynamic evolution and biogenesis of small rnas during sex reversal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421800/
https://www.ncbi.nlm.nih.gov/pubmed/25944477
http://dx.doi.org/10.1038/srep09999
work_keys_str_mv AT liujie dynamicevolutionandbiogenesisofsmallrnasduringsexreversal
AT luomajing dynamicevolutionandbiogenesisofsmallrnasduringsexreversal
AT shengyue dynamicevolutionandbiogenesisofsmallrnasduringsexreversal
AT hongqiang dynamicevolutionandbiogenesisofsmallrnasduringsexreversal
AT chenghanhua dynamicevolutionandbiogenesisofsmallrnasduringsexreversal
AT zhourongjia dynamicevolutionandbiogenesisofsmallrnasduringsexreversal