Cargando…

Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination

Some differentially expressed genes (DEGs) that encode key enzymes involved in steroidogenic biosynthesis (CYP19A1) and key molecules related to gonadal functions (DMRT1, SOX9, AMH, FOXL2, WNT4, RSPO2, and GDF9) have been identified in adult gonadal RNA-seq studies of Reeves’ pond turtle (Mauremys r...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiong, Lei, Yang, Mengli, Zheng, Kai, Wang, Ziming, Gu, Shengli, Tong, Jiucui, Liu, Jianjun, Shah, Nadar Ali, Nie, Liuwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061903/
https://www.ncbi.nlm.nih.gov/pubmed/32194623
http://dx.doi.org/10.3389/fgene.2020.00133
_version_ 1783504462382366720
author Xiong, Lei
Yang, Mengli
Zheng, Kai
Wang, Ziming
Gu, Shengli
Tong, Jiucui
Liu, Jianjun
Shah, Nadar Ali
Nie, Liuwang
author_facet Xiong, Lei
Yang, Mengli
Zheng, Kai
Wang, Ziming
Gu, Shengli
Tong, Jiucui
Liu, Jianjun
Shah, Nadar Ali
Nie, Liuwang
author_sort Xiong, Lei
collection PubMed
description Some differentially expressed genes (DEGs) that encode key enzymes involved in steroidogenic biosynthesis (CYP19A1) and key molecules related to gonadal functions (DMRT1, SOX9, AMH, FOXL2, WNT4, RSPO2, and GDF9) have been identified in adult gonadal RNA-seq studies of Reeves’ pond turtle (Mauremys reevesii) with temperature-dependent sex determination (TSD). Gonadal functional maintenance and gametogenesis comprises a highly regulated and coordinated biological process, and increasing evidence indicates that microRNAs (miRNAs) may be involved in this dynamic program. However, it is not clear how the regulatory network comprising miRNAs changes the expression levels of these genes. In this study, miRNA sequencing of adult testis and ovary tissues from M. reevesii detected 25 known and 379 novel miRNAs, where 60 miRNAs were differentially expressed in the testis and ovary. A total of 1,477 target genes based on the differentially expressed miRNAs were predicted, where 221 target genes also exhibited differential expression. To verify the accuracy of the sequencing data, 10 differentially expressed miRNAs were validated by quantitative reverse transcription real-time PCR, and were found to be consistent with the transcriptome sequencing results. Moreover, several miRNA/target gene pairs, i.e., mre-let-7a-5p/mre-let-7e-5p and CYP19A1, mre-miR-200a-3p and DMRT1, mre-miR-101-3p and SOX9, and mre-miR-138-5p and AMH were identified. To explore the regulatory role of miRNAs, we conducted target gene enrichment analysis of the miRNAs and 221 target genes in the regulatory network. The signaling pathways related to gonadal functional maintenance and gametogenesis based on the DEGs and target genes were then compared. Our findings provide crucial information to facilitate further research into the regulatory mechanisms involving miRNAs in turtle species with TSD.
format Online
Article
Text
id pubmed-7061903
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-70619032020-03-19 Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination Xiong, Lei Yang, Mengli Zheng, Kai Wang, Ziming Gu, Shengli Tong, Jiucui Liu, Jianjun Shah, Nadar Ali Nie, Liuwang Front Genet Genetics Some differentially expressed genes (DEGs) that encode key enzymes involved in steroidogenic biosynthesis (CYP19A1) and key molecules related to gonadal functions (DMRT1, SOX9, AMH, FOXL2, WNT4, RSPO2, and GDF9) have been identified in adult gonadal RNA-seq studies of Reeves’ pond turtle (Mauremys reevesii) with temperature-dependent sex determination (TSD). Gonadal functional maintenance and gametogenesis comprises a highly regulated and coordinated biological process, and increasing evidence indicates that microRNAs (miRNAs) may be involved in this dynamic program. However, it is not clear how the regulatory network comprising miRNAs changes the expression levels of these genes. In this study, miRNA sequencing of adult testis and ovary tissues from M. reevesii detected 25 known and 379 novel miRNAs, where 60 miRNAs were differentially expressed in the testis and ovary. A total of 1,477 target genes based on the differentially expressed miRNAs were predicted, where 221 target genes also exhibited differential expression. To verify the accuracy of the sequencing data, 10 differentially expressed miRNAs were validated by quantitative reverse transcription real-time PCR, and were found to be consistent with the transcriptome sequencing results. Moreover, several miRNA/target gene pairs, i.e., mre-let-7a-5p/mre-let-7e-5p and CYP19A1, mre-miR-200a-3p and DMRT1, mre-miR-101-3p and SOX9, and mre-miR-138-5p and AMH were identified. To explore the regulatory role of miRNAs, we conducted target gene enrichment analysis of the miRNAs and 221 target genes in the regulatory network. The signaling pathways related to gonadal functional maintenance and gametogenesis based on the DEGs and target genes were then compared. Our findings provide crucial information to facilitate further research into the regulatory mechanisms involving miRNAs in turtle species with TSD. Frontiers Media S.A. 2020-03-02 /pmc/articles/PMC7061903/ /pubmed/32194623 http://dx.doi.org/10.3389/fgene.2020.00133 Text en Copyright © 2020 Xiong, Yang, Zheng, Wang, Gu, Tong, Liu, Shah and Nie http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Xiong, Lei
Yang, Mengli
Zheng, Kai
Wang, Ziming
Gu, Shengli
Tong, Jiucui
Liu, Jianjun
Shah, Nadar Ali
Nie, Liuwang
Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination
title Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination
title_full Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination
title_fullStr Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination
title_full_unstemmed Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination
title_short Comparison of Adult Testis and Ovary MicroRNA Expression Profiles in Reeves’ Pond Turtles (Mauremys reevesii) With Temperature-Dependent Sex Determination
title_sort comparison of adult testis and ovary microrna expression profiles in reeves’ pond turtles (mauremys reevesii) with temperature-dependent sex determination
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061903/
https://www.ncbi.nlm.nih.gov/pubmed/32194623
http://dx.doi.org/10.3389/fgene.2020.00133
work_keys_str_mv AT xionglei comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT yangmengli comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT zhengkai comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT wangziming comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT gushengli comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT tongjiucui comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT liujianjun comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT shahnadarali comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination
AT nieliuwang comparisonofadulttestisandovarymicrornaexpressionprofilesinreevespondturtlesmauremysreevesiiwithtemperaturedependentsexdetermination