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Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi

Interspecific hybridization may lead to sterility and/or inviability through differential expression of genes and transposable elements (TEs). In Drosophila, studies have reported massive TE mobilization in hybrids from interspecific crosses of species presenting high divergence times. However, few...

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Autores principales: Banho, Cecília Artico, Oliveira, Daniel Siqueira, Haudry, Annabelle, Fablet, Marie, Vieira, Cristina, Carareto, Claudia Marcia Aparecida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700503/
https://www.ncbi.nlm.nih.gov/pubmed/34944084
http://dx.doi.org/10.3390/cells10123574
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author Banho, Cecília Artico
Oliveira, Daniel Siqueira
Haudry, Annabelle
Fablet, Marie
Vieira, Cristina
Carareto, Claudia Marcia Aparecida
author_facet Banho, Cecília Artico
Oliveira, Daniel Siqueira
Haudry, Annabelle
Fablet, Marie
Vieira, Cristina
Carareto, Claudia Marcia Aparecida
author_sort Banho, Cecília Artico
collection PubMed
description Interspecific hybridization may lead to sterility and/or inviability through differential expression of genes and transposable elements (TEs). In Drosophila, studies have reported massive TE mobilization in hybrids from interspecific crosses of species presenting high divergence times. However, few studies have examined the consequences of TE mobilization upon hybridization in recently diverged species, such as Drosophila arizonae and D. mojavensis. We have sequenced transcriptomes of D. arizonae and the subspecies D. m. wrigleyi and their reciprocal hybrids, as well as piRNAs, to analyze the impact of genomic stress on TE regulation. Our results revealed that the differential expression in both gonadal tissues of parental species was similar. Globally, ovaries and testes showed few deregulated TEs compared with both parental lines. Analyses of small RNA data showed that in ovaries, the TE upregulation is likely due to divergence of copies inherited from parental genomes and lack of piRNAs mapping to them. Nevertheless, in testes, the divergent expression of genes associated with chromatin state and piRNA pathway potentially indicates that TE differential expression is related to the divergence of regulatory genes that play a role in modulating transcriptional and post-transcriptional mechanisms.
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spelling pubmed-87005032021-12-24 Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi Banho, Cecília Artico Oliveira, Daniel Siqueira Haudry, Annabelle Fablet, Marie Vieira, Cristina Carareto, Claudia Marcia Aparecida Cells Article Interspecific hybridization may lead to sterility and/or inviability through differential expression of genes and transposable elements (TEs). In Drosophila, studies have reported massive TE mobilization in hybrids from interspecific crosses of species presenting high divergence times. However, few studies have examined the consequences of TE mobilization upon hybridization in recently diverged species, such as Drosophila arizonae and D. mojavensis. We have sequenced transcriptomes of D. arizonae and the subspecies D. m. wrigleyi and their reciprocal hybrids, as well as piRNAs, to analyze the impact of genomic stress on TE regulation. Our results revealed that the differential expression in both gonadal tissues of parental species was similar. Globally, ovaries and testes showed few deregulated TEs compared with both parental lines. Analyses of small RNA data showed that in ovaries, the TE upregulation is likely due to divergence of copies inherited from parental genomes and lack of piRNAs mapping to them. Nevertheless, in testes, the divergent expression of genes associated with chromatin state and piRNA pathway potentially indicates that TE differential expression is related to the divergence of regulatory genes that play a role in modulating transcriptional and post-transcriptional mechanisms. MDPI 2021-12-18 /pmc/articles/PMC8700503/ /pubmed/34944084 http://dx.doi.org/10.3390/cells10123574 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Banho, Cecília Artico
Oliveira, Daniel Siqueira
Haudry, Annabelle
Fablet, Marie
Vieira, Cristina
Carareto, Claudia Marcia Aparecida
Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi
title Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi
title_full Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi
title_fullStr Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi
title_full_unstemmed Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi
title_short Transposable Element Expression and Regulation Profile in Gonads of Interspecific Hybrids of Drosophila arizonae and Drosophila mojavensis wrigleyi
title_sort transposable element expression and regulation profile in gonads of interspecific hybrids of drosophila arizonae and drosophila mojavensis wrigleyi
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700503/
https://www.ncbi.nlm.nih.gov/pubmed/34944084
http://dx.doi.org/10.3390/cells10123574
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