Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma

Endogenous retroviruses (ERVs) are remnants of ancestral retroviruses that infected host germ cells in the past. Most ERVs are thought to be non-functional elements, but some ERVs retain open reading frames (ORFs) capable of expressing proteins. The proteins encoded by ERV-ORFs have potential roles...

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Main Authors: Koichi Kitao, Aoi Sumiyoshi, So Nakagawa, Yuki Matsumoto, Takuya Mizuno, Takayuki Miyazawa
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-11-01
Series:Frontiers in Virology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fviro.2021.785678/full
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author Koichi Kitao
Aoi Sumiyoshi
So Nakagawa
Yuki Matsumoto
Takuya Mizuno
Takayuki Miyazawa
author_facet Koichi Kitao
Aoi Sumiyoshi
So Nakagawa
Yuki Matsumoto
Takuya Mizuno
Takayuki Miyazawa
author_sort Koichi Kitao
collection DOAJ
description Endogenous retroviruses (ERVs) are remnants of ancestral retroviruses that infected host germ cells in the past. Most ERVs are thought to be non-functional elements, but some ERVs retain open reading frames (ORFs) capable of expressing proteins. The proteins encoded by ERV-ORFs have potential roles in oncogenesis; however, studies on mammals other than humans and mice are limited. Here, we identified ERV-derived genes expressed in canine oral malignant melanoma (OMM). We identified 11 ERV-derived genes in our OMM samples. Differential expression gene analysis revealed that four ERV-derived genes (PEG10, LOC102155597, and two newly identified genes) were upregulated in OMM compared to healthy tissues. PEG10 is a conserved long terminal repeat (LTR)-type retrotransposon-derived gene among mammals and is involved in human cancers. LOC102155597 is a retroviral env gene conserved in Carnivora. This Env protein harbors an immunosuppressive domain, implying the potential adverse effects on the immune system. While the production of viral particles from ERVs has been reported in human and mouse melanoma, we found no ERV-derived genes having the potential to produce viral particles. These results provide insights into the different and conserved features of ERV-derived genes in mammalian melanoma.
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spelling doaj.art-5499fddd22434850a7866ce4dcdd2eca2022-12-21T19:51:40ZengFrontiers Media S.A.Frontiers in Virology2673-818X2021-11-01110.3389/fviro.2021.785678785678Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant MelanomaKoichi Kitao0Aoi Sumiyoshi1So Nakagawa2Yuki Matsumoto3Takuya Mizuno4Takayuki Miyazawa5Laboratory of Virus-Host Coevolution, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, JapanLaboratory of Virus-Host Coevolution, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, JapanDepartment of Molecular Life Science, Tokai University School of Medicine, Isehara, JapanResearch and Development Section, Anicom Specialty Medical Institute Inc., Kanagawa, JapanLabratory of Molecular Diagnostics and Therapeutics, The United Graduate School of Veterinary Medicine, Yamaguchi University, Yamaguchi, JapanLaboratory of Virus-Host Coevolution, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, JapanEndogenous retroviruses (ERVs) are remnants of ancestral retroviruses that infected host germ cells in the past. Most ERVs are thought to be non-functional elements, but some ERVs retain open reading frames (ORFs) capable of expressing proteins. The proteins encoded by ERV-ORFs have potential roles in oncogenesis; however, studies on mammals other than humans and mice are limited. Here, we identified ERV-derived genes expressed in canine oral malignant melanoma (OMM). We identified 11 ERV-derived genes in our OMM samples. Differential expression gene analysis revealed that four ERV-derived genes (PEG10, LOC102155597, and two newly identified genes) were upregulated in OMM compared to healthy tissues. PEG10 is a conserved long terminal repeat (LTR)-type retrotransposon-derived gene among mammals and is involved in human cancers. LOC102155597 is a retroviral env gene conserved in Carnivora. This Env protein harbors an immunosuppressive domain, implying the potential adverse effects on the immune system. While the production of viral particles from ERVs has been reported in human and mouse melanoma, we found no ERV-derived genes having the potential to produce viral particles. These results provide insights into the different and conserved features of ERV-derived genes in mammalian melanoma.https://www.frontiersin.org/articles/10.3389/fviro.2021.785678/fulldogendogenous retrovirusoral malignant melanomaprotein-coding geneRNA-Seq
spellingShingle Koichi Kitao
Aoi Sumiyoshi
So Nakagawa
Yuki Matsumoto
Takuya Mizuno
Takayuki Miyazawa
Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma
Frontiers in Virology
dog
endogenous retrovirus
oral malignant melanoma
protein-coding gene
RNA-Seq
title Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma
title_full Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma
title_fullStr Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma
title_full_unstemmed Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma
title_short Systematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma
title_sort systematic identification of endogenous retroviral protein coding genes expressed in canine oral malignant melanoma
topic dog
endogenous retrovirus
oral malignant melanoma
protein-coding gene
RNA-Seq
url https://www.frontiersin.org/articles/10.3389/fviro.2021.785678/full
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AT sonakagawa systematicidentificationofendogenousretroviralproteincodinggenesexpressedincanineoralmalignantmelanoma
AT yukimatsumoto systematicidentificationofendogenousretroviralproteincodinggenesexpressedincanineoralmalignantmelanoma
AT takuyamizuno systematicidentificationofendogenousretroviralproteincodinggenesexpressedincanineoralmalignantmelanoma
AT takayukimiyazawa systematicidentificationofendogenousretroviralproteincodinggenesexpressedincanineoralmalignantmelanoma