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Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes

Endogenous virus elements (EVEs) are viral-derived sequences integrated into their host genomes. EVEs of the Jingchuvirales order were detected in a wide range of insect genomes covering several distantly related families. Moreover, Jingchuvirales-derived glycoproteins were recently associated by ou...

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Autores principales: Dezordi, Filipe Zimmer, Coutinho, Gutembergmann Batista, Dias, Yago José Mariz, Wallau, Gabriel Luz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084718/
https://www.ncbi.nlm.nih.gov/pubmed/37036390
http://dx.doi.org/10.1590/1678-4685-GMB-2022-0218
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author Dezordi, Filipe Zimmer
Coutinho, Gutembergmann Batista
Dias, Yago José Mariz
Wallau, Gabriel Luz
author_facet Dezordi, Filipe Zimmer
Coutinho, Gutembergmann Batista
Dias, Yago José Mariz
Wallau, Gabriel Luz
author_sort Dezordi, Filipe Zimmer
collection PubMed
description Endogenous virus elements (EVEs) are viral-derived sequences integrated into their host genomes. EVEs of the Jingchuvirales order were detected in a wide range of insect genomes covering several distantly related families. Moreover, Jingchuvirales-derived glycoproteins were recently associated by our group with the origin of a putative new retrovirus based on a glycoprotein captured by a mosquito retrotransposon. But, except for mosquitoes, there is a lack of a more detailed understanding of the endogenization mechanism, timing, and frequency per Jingchuvirales viral lineages. Here we screened Jingchuvirales glycoprotein-derived EVEs (Jg-EVEs) in eukaryotic genomes. We found six distinct endogenization events of Jg-EVEs, that belong to two out of five known Jingchuvirales families (Chuviridae and Natareviridae). For seven arthropod families bearing Jg-EVEs there is no register of bona fide circulating chuvirus infection. Hence, our results show that Jingchuvirales viruses infected or still infect these host families. Although we found abundant evidence of LTR-Gypsy retrotransposons fragments associated with the glycoprotein in Hymenoptera and other insect orders, our results show that the widespread distribution of Jingchuvirales glycoproteins in extant Arhtropods is a result of multiple ancient endogenization events and that these virus fossils are being vertically inherited in Arthropods genomes for millions of years.
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spelling pubmed-100847182023-04-11 Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes Dezordi, Filipe Zimmer Coutinho, Gutembergmann Batista Dias, Yago José Mariz Wallau, Gabriel Luz Genet Mol Biol Genomics and Bioinformatics Endogenous virus elements (EVEs) are viral-derived sequences integrated into their host genomes. EVEs of the Jingchuvirales order were detected in a wide range of insect genomes covering several distantly related families. Moreover, Jingchuvirales-derived glycoproteins were recently associated by our group with the origin of a putative new retrovirus based on a glycoprotein captured by a mosquito retrotransposon. But, except for mosquitoes, there is a lack of a more detailed understanding of the endogenization mechanism, timing, and frequency per Jingchuvirales viral lineages. Here we screened Jingchuvirales glycoprotein-derived EVEs (Jg-EVEs) in eukaryotic genomes. We found six distinct endogenization events of Jg-EVEs, that belong to two out of five known Jingchuvirales families (Chuviridae and Natareviridae). For seven arthropod families bearing Jg-EVEs there is no register of bona fide circulating chuvirus infection. Hence, our results show that Jingchuvirales viruses infected or still infect these host families. Although we found abundant evidence of LTR-Gypsy retrotransposons fragments associated with the glycoprotein in Hymenoptera and other insect orders, our results show that the widespread distribution of Jingchuvirales glycoproteins in extant Arhtropods is a result of multiple ancient endogenization events and that these virus fossils are being vertically inherited in Arthropods genomes for millions of years. Sociedade Brasileira de Genética 2023-04-07 /pmc/articles/PMC10084718/ /pubmed/37036390 http://dx.doi.org/10.1590/1678-4685-GMB-2022-0218 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Genomics and Bioinformatics
Dezordi, Filipe Zimmer
Coutinho, Gutembergmann Batista
Dias, Yago José Mariz
Wallau, Gabriel Luz
Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes
title Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes
title_full Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes
title_fullStr Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes
title_full_unstemmed Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes
title_short Ancient origin of Jingchuvirales derived glycoproteins integrated in arthropod genomes
title_sort ancient origin of jingchuvirales derived glycoproteins integrated in arthropod genomes
topic Genomics and Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084718/
https://www.ncbi.nlm.nih.gov/pubmed/37036390
http://dx.doi.org/10.1590/1678-4685-GMB-2022-0218
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