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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Autores principales: Koichi Kitao, Aoi Sumiyoshi, So Nakagawa, Yuki Matsumoto, Takuya Mizuno, Takayuki Miyazawa
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Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/5499fddd22434850a7866ce4dcdd2eca
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spelling oai:doaj.org-article:5499fddd22434850a7866ce4dcdd2eca2021-11-30T16:10:52ZSystematic Identification of Endogenous Retroviral Protein-Coding Genes Expressed in Canine Oral Malignant Melanoma2673-818X10.3389/fviro.2021.785678https://doaj.org/article/5499fddd22434850a7866ce4dcdd2eca2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fviro.2021.785678/fullhttps://doaj.org/toc/2673-818XEndogenous 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.Koichi KitaoAoi SumiyoshiSo NakagawaYuki MatsumotoTakuya MizunoTakayuki MiyazawaFrontiers Media S.A.articledogendogenous retrovirusoral malignant melanomaprotein-coding geneRNA-SeqMicrobiologyQR1-502ENFrontiers in Virology, Vol 1 (2021)
institution DOAJ
collection DOAJ
language EN
topic dog
endogenous retrovirus
oral malignant melanoma
protein-coding gene
RNA-Seq
Microbiology
QR1-502
spellingShingle dog
endogenous retrovirus
oral malignant melanoma
protein-coding gene
RNA-Seq
Microbiology
QR1-502
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
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.
format article
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
title 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_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_sort systematic identification of endogenous retroviral protein-coding genes expressed in canine oral malignant melanoma
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/5499fddd22434850a7866ce4dcdd2eca
work_keys_str_mv AT koichikitao systematicidentificationofendogenousretroviralproteincodinggenesexpressedincanineoralmalignantmelanoma
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