Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22
Abstract Background The human genome contains remnants of ancient retroviral infections called human endogenous retroviruses (HERV). Their expression is often observed in several diseases of autoimmune or inflammatory nature. However, the exact biological mechanisms induced by HERVs are still poorly...
Main Authors: | , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-05-01
|
Series: | Immunity & Ageing |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12979-020-00182-0 |
_version_ | 1817988877724418048 |
---|---|
author | Arttu Autio Tapio Nevalainen Binisha H. Mishra Marja Jylhä Heini Flinck Mikko Hurme |
author_facet | Arttu Autio Tapio Nevalainen Binisha H. Mishra Marja Jylhä Heini Flinck Mikko Hurme |
author_sort | Arttu Autio |
collection | DOAJ |
description | Abstract Background The human genome contains remnants of ancient retroviral infections called human endogenous retroviruses (HERV). Their expression is often observed in several diseases of autoimmune or inflammatory nature. However, the exact biological mechanisms induced by HERVs are still poorly understood. We have previously shown that several HERVs of the HERV-K (HML-2) family are strongly transcribed in the peripheral blood mononuclear cells (PBMC) derived from young and old individuals. To examine the potential functional consequences of HERV-K (HML-2) expression, we have now analyzed the correlation of its expression with age-associated changes in the transcriptome using gene set enrichment analysis (GSEA). We focused our analysis on the HERV-K (HML-2) provirus at 1q22, also known as ERVK-7. Results The genes strongly correlating with the expression of HERV-K (HML-2) provirus at 1q22 expression were found to be almost entirely different in young and old individuals. The number of genes strongly correlating (Pearson correlation coefficient ≥ 0.7) with 1q22 expression was 946 genes in the old and 435 in the young, of which only 41 genes correlated strongly in both. Consequently, the related gene ontology (GO) biological processes were different. In the older individuals, many of the highest correlating processes relate to the function of neutrophils. Conclusions The results of this work suggest that the biological processes associated with the expression of HERV-K (HML-2) provirus at 1q22 are different in the blood of young and old individuals. Specifically, a strong association was found in the older individuals between neutrophil activity and the expression of the HERV-K (HML-2) provirus at 1q22. These findings offer insight into potential effects of altered HERV expression in older individuals. |
first_indexed | 2024-04-14T00:40:01Z |
format | Article |
id | doaj.art-d19b68de86394b42a1301fc93d4cc3a7 |
institution | Directory Open Access Journal |
issn | 1742-4933 |
language | English |
last_indexed | 2024-04-14T00:40:01Z |
publishDate | 2020-05-01 |
publisher | BMC |
record_format | Article |
series | Immunity & Ageing |
spelling | doaj.art-d19b68de86394b42a1301fc93d4cc3a72022-12-22T02:22:14ZengBMCImmunity & Ageing1742-49332020-05-011711810.1186/s12979-020-00182-0Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22Arttu Autio0Tapio Nevalainen1Binisha H. Mishra2Marja Jylhä3Heini Flinck4Mikko Hurme5Faculty of Medicine and Health Technology, Tampere UniversityFaculty of Medicine and Health Technology, Tampere UniversityDepartment of Clinical Chemistry, Faculty of Medicine and Health Technology, Tampere UniversityGerontology Research Center (GEREC)Department of Clinical Microbiology, Fimlab LaboratoriesFaculty of Medicine and Health Technology, Tampere UniversityAbstract Background The human genome contains remnants of ancient retroviral infections called human endogenous retroviruses (HERV). Their expression is often observed in several diseases of autoimmune or inflammatory nature. However, the exact biological mechanisms induced by HERVs are still poorly understood. We have previously shown that several HERVs of the HERV-K (HML-2) family are strongly transcribed in the peripheral blood mononuclear cells (PBMC) derived from young and old individuals. To examine the potential functional consequences of HERV-K (HML-2) expression, we have now analyzed the correlation of its expression with age-associated changes in the transcriptome using gene set enrichment analysis (GSEA). We focused our analysis on the HERV-K (HML-2) provirus at 1q22, also known as ERVK-7. Results The genes strongly correlating with the expression of HERV-K (HML-2) provirus at 1q22 expression were found to be almost entirely different in young and old individuals. The number of genes strongly correlating (Pearson correlation coefficient ≥ 0.7) with 1q22 expression was 946 genes in the old and 435 in the young, of which only 41 genes correlated strongly in both. Consequently, the related gene ontology (GO) biological processes were different. In the older individuals, many of the highest correlating processes relate to the function of neutrophils. Conclusions The results of this work suggest that the biological processes associated with the expression of HERV-K (HML-2) provirus at 1q22 are different in the blood of young and old individuals. Specifically, a strong association was found in the older individuals between neutrophil activity and the expression of the HERV-K (HML-2) provirus at 1q22. These findings offer insight into potential effects of altered HERV expression in older individuals.http://link.springer.com/article/10.1186/s12979-020-00182-0Human endogenous retrovirusHERV-K (HML-2)ERVK-7ImmunosenescenceGSEANext-generation sequencing |
spellingShingle | Arttu Autio Tapio Nevalainen Binisha H. Mishra Marja Jylhä Heini Flinck Mikko Hurme Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22 Immunity & Ageing Human endogenous retrovirus HERV-K (HML-2) ERVK-7 Immunosenescence GSEA Next-generation sequencing |
title | Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22 |
title_full | Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22 |
title_fullStr | Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22 |
title_full_unstemmed | Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22 |
title_short | Effect of aging on the transcriptomic changes associated with the expression of the HERV-K (HML-2) provirus at 1q22 |
title_sort | effect of aging on the transcriptomic changes associated with the expression of the herv k hml 2 provirus at 1q22 |
topic | Human endogenous retrovirus HERV-K (HML-2) ERVK-7 Immunosenescence GSEA Next-generation sequencing |
url | http://link.springer.com/article/10.1186/s12979-020-00182-0 |
work_keys_str_mv | AT arttuautio effectofagingonthetranscriptomicchangesassociatedwiththeexpressionofthehervkhml2provirusat1q22 AT tapionevalainen effectofagingonthetranscriptomicchangesassociatedwiththeexpressionofthehervkhml2provirusat1q22 AT binishahmishra effectofagingonthetranscriptomicchangesassociatedwiththeexpressionofthehervkhml2provirusat1q22 AT marjajylha effectofagingonthetranscriptomicchangesassociatedwiththeexpressionofthehervkhml2provirusat1q22 AT heiniflinck effectofagingonthetranscriptomicchangesassociatedwiththeexpressionofthehervkhml2provirusat1q22 AT mikkohurme effectofagingonthetranscriptomicchangesassociatedwiththeexpressionofthehervkhml2provirusat1q22 |