Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues
Human endogenous retrovirus (HERV) transcripts are known to be highly expressed in cancers, yet their activity in nondiseased tissue is largely unknown. Using the GTEx RNA-seq dataset from normal tissue sampled at autopsy, we characterized individual expression of the recent HERV-K (HML-2) provirus...
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Public Library of Science (PLoS)
2022-10-01
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Series: | PLoS Biology |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578601/?tool=EBI |
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author | Aidan Burn Farrah Roy Michael Freeman John M. Coffin |
author_facet | Aidan Burn Farrah Roy Michael Freeman John M. Coffin |
author_sort | Aidan Burn |
collection | DOAJ |
description | Human endogenous retrovirus (HERV) transcripts are known to be highly expressed in cancers, yet their activity in nondiseased tissue is largely unknown. Using the GTEx RNA-seq dataset from normal tissue sampled at autopsy, we characterized individual expression of the recent HERV-K (HML-2) provirus group across 13,000 different samples of 54 different tissues from 948 individuals. HML-2 transcripts could be identified in every tissue sampled and were elevated in the cerebellum, pituitary, testis, and thyroid. A total of 37 different individual proviruses were expressed in 1 or more tissues, representing all 3 LTR5 subgroups. Nine proviruses were identified as having long terminal repeat (LTR)-driven transcription, 7 of which belonged to the most recent LTR5HS subgroup. Proviruses of different subgroups displayed a bias in tissue expression, which may be associated with differences in transcription factor binding sites in their LTRs. Provirus expression was greater in evolutionarily older proviruses with an earliest shared ancestor of gorilla or older. HML-2 expression was significantly affected by biological sex in 1 tissue, while age and timing of death (Hardy score) had little effect. Proviruses containing intact gag, pro, and env open reading frames (ORFs) were expressed in the dataset, with almost every tissue measured potentially expressing at least 1 intact ORF (gag). Human endogenous retrovirus (HERV) transcripts are known to be highly expressed in cancers, but what is their activity in normal tissue? This study uses unique patterns of HERV-K RNA expression in the large GEx dataset from non-diseased tissue sites to provide new insights into both the coevolution of HERV-K with our primate ancestors and their current role in human biology. |
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issn | 1544-9173 1545-7885 |
language | English |
last_indexed | 2024-04-11T19:18:16Z |
publishDate | 2022-10-01 |
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series | PLoS Biology |
spelling | doaj.art-cb87a8feda964ff3b3a84740b3827ab12022-12-22T04:07:23ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852022-10-012010Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissuesAidan BurnFarrah RoyMichael FreemanJohn M. CoffinHuman endogenous retrovirus (HERV) transcripts are known to be highly expressed in cancers, yet their activity in nondiseased tissue is largely unknown. Using the GTEx RNA-seq dataset from normal tissue sampled at autopsy, we characterized individual expression of the recent HERV-K (HML-2) provirus group across 13,000 different samples of 54 different tissues from 948 individuals. HML-2 transcripts could be identified in every tissue sampled and were elevated in the cerebellum, pituitary, testis, and thyroid. A total of 37 different individual proviruses were expressed in 1 or more tissues, representing all 3 LTR5 subgroups. Nine proviruses were identified as having long terminal repeat (LTR)-driven transcription, 7 of which belonged to the most recent LTR5HS subgroup. Proviruses of different subgroups displayed a bias in tissue expression, which may be associated with differences in transcription factor binding sites in their LTRs. Provirus expression was greater in evolutionarily older proviruses with an earliest shared ancestor of gorilla or older. HML-2 expression was significantly affected by biological sex in 1 tissue, while age and timing of death (Hardy score) had little effect. Proviruses containing intact gag, pro, and env open reading frames (ORFs) were expressed in the dataset, with almost every tissue measured potentially expressing at least 1 intact ORF (gag). Human endogenous retrovirus (HERV) transcripts are known to be highly expressed in cancers, but what is their activity in normal tissue? This study uses unique patterns of HERV-K RNA expression in the large GEx dataset from non-diseased tissue sites to provide new insights into both the coevolution of HERV-K with our primate ancestors and their current role in human biology.https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578601/?tool=EBI |
spellingShingle | Aidan Burn Farrah Roy Michael Freeman John M. Coffin Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues PLoS Biology |
title | Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues |
title_full | Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues |
title_fullStr | Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues |
title_full_unstemmed | Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues |
title_short | Widespread expression of the ancient HERV-K (HML-2) provirus group in normal human tissues |
title_sort | widespread expression of the ancient herv k hml 2 provirus group in normal human tissues |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9578601/?tool=EBI |
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