Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs
Despite the absence of a confirmed exogenously replicating retrovirus in Canis lupus familiaris ( C . familiaris ), past retroviral infections are evident in the genomes of living animals via the presence of endogenous retroviruses (ERVs). Although gammaretrovirus-like transcripts and enzyme activit...
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Online Access: | http://dx.doi.org/10.1371/journal.pgen.1011083 https://dx.plos.org/10.1371/journal.pgen.1011083 |
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crplos:10.1371/journal.pgen.1011083 2024-10-29T17:42:35+00:00 Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs Jarosz, Abigail S. Pendleton, Amanda L. Lashbrook, Michael J. Cech, Erica Altieri, Madison Kunch, Austin Modiano, Jaime F. Halo, Julia V. Murphy, William J. National Institute of General Medical Sciences 2023 http://dx.doi.org/10.1371/journal.pgen.1011083 https://dx.plos.org/10.1371/journal.pgen.1011083 en eng Public Library of Science (PLoS) http://creativecommons.org/licenses/by/4.0/ PLOS Genetics volume 19, issue 12, page e1011083 ISSN 1553-7404 journal-article 2023 crplos https://doi.org/10.1371/journal.pgen.1011083 2024-10-01T04:05:59Z Despite the absence of a confirmed exogenously replicating retrovirus in Canis lupus familiaris ( C . familiaris ), past retroviral infections are evident in the genomes of living animals via the presence of endogenous retroviruses (ERVs). Although gammaretrovirus-like transcripts and enzyme activities were previously reported to be present in canine leukemias and lymphomas, those findings were not further explored. Initial analysis of the C . familiaris reference genome revealed a minor subset of one ERV lineage, classified as CfERV-Fc1(a), or Fc1(a) here, with features characteristic of recent integration, including the presence of ORFs and identical or nearly identical LTRs. Our previous analysis of whole genome sequence data belonging to extant Canidae revealed a burst of past infections in Canis ancestors resulting in numerous young, polymorphic, and highly intact loci now segregating in dogs. Here, we demonstrate the expression of full-length Fc1(a) proviruses in tissues collected from healthy animals and from animals with cancer. We observed significantly higher expression in samples of dogs with various cancer diagnoses when compared to samples from healthy dogs. Genotyping of insertionally polymorphic Fc1(a) loci identified candidate expressed proviruses and delineated distributions over sample groups. Collectively, the data show that Fc1(a) proviruses retain biological activity in the domestic dog and provides a means to examine potential genetic links with disease states in this species. Article in Journal/Newspaper Canis lupus PLOS PLOS Genetics 19 12 e1011083 |
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English |
description |
Despite the absence of a confirmed exogenously replicating retrovirus in Canis lupus familiaris ( C . familiaris ), past retroviral infections are evident in the genomes of living animals via the presence of endogenous retroviruses (ERVs). Although gammaretrovirus-like transcripts and enzyme activities were previously reported to be present in canine leukemias and lymphomas, those findings were not further explored. Initial analysis of the C . familiaris reference genome revealed a minor subset of one ERV lineage, classified as CfERV-Fc1(a), or Fc1(a) here, with features characteristic of recent integration, including the presence of ORFs and identical or nearly identical LTRs. Our previous analysis of whole genome sequence data belonging to extant Canidae revealed a burst of past infections in Canis ancestors resulting in numerous young, polymorphic, and highly intact loci now segregating in dogs. Here, we demonstrate the expression of full-length Fc1(a) proviruses in tissues collected from healthy animals and from animals with cancer. We observed significantly higher expression in samples of dogs with various cancer diagnoses when compared to samples from healthy dogs. Genotyping of insertionally polymorphic Fc1(a) loci identified candidate expressed proviruses and delineated distributions over sample groups. Collectively, the data show that Fc1(a) proviruses retain biological activity in the domestic dog and provides a means to examine potential genetic links with disease states in this species. |
author2 |
Murphy, William J. National Institute of General Medical Sciences |
format |
Article in Journal/Newspaper |
author |
Jarosz, Abigail S. Pendleton, Amanda L. Lashbrook, Michael J. Cech, Erica Altieri, Madison Kunch, Austin Modiano, Jaime F. Halo, Julia V. |
spellingShingle |
Jarosz, Abigail S. Pendleton, Amanda L. Lashbrook, Michael J. Cech, Erica Altieri, Madison Kunch, Austin Modiano, Jaime F. Halo, Julia V. Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
author_facet |
Jarosz, Abigail S. Pendleton, Amanda L. Lashbrook, Michael J. Cech, Erica Altieri, Madison Kunch, Austin Modiano, Jaime F. Halo, Julia V. |
author_sort |
Jarosz, Abigail S. |
title |
Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
title_short |
Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
title_full |
Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
title_fullStr |
Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
title_full_unstemmed |
Expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
title_sort |
expression and high levels of insertional polymorphism of an endogenous gammaretrovirus lineage in dogs |
publisher |
Public Library of Science (PLoS) |
publishDate |
2023 |
url |
http://dx.doi.org/10.1371/journal.pgen.1011083 https://dx.plos.org/10.1371/journal.pgen.1011083 |
genre |
Canis lupus |
genre_facet |
Canis lupus |
op_source |
PLOS Genetics volume 19, issue 12, page e1011083 ISSN 1553-7404 |
op_rights |
http://creativecommons.org/licenses/by/4.0/ |
op_doi |
https://doi.org/10.1371/journal.pgen.1011083 |
container_title |
PLOS Genetics |
container_volume |
19 |
container_issue |
12 |
container_start_page |
e1011083 |
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1814279736203935744 |