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Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin

Human endogenous retrovirus (HERV) sequences make up at least 8% of the human genome. Transcripts originating from these loci as well as proteins encoded by them have been detected in various tissues. HERVs are believed to be implicated in autoimmune diseases, however the extent to which, has remain...

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Autores principales: Lättekivi, Freddy, Kõks, Sulev, Keermann, Maris, Reimann, Ene, Prans, Ele, Abram, Kristi, Silm, Helgi, Kõks, Gea, Kingo, Külli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847543/
https://www.ncbi.nlm.nih.gov/pubmed/29531256
http://dx.doi.org/10.1038/s41598-018-22734-7
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author Lättekivi, Freddy
Kõks, Sulev
Keermann, Maris
Reimann, Ene
Prans, Ele
Abram, Kristi
Silm, Helgi
Kõks, Gea
Kingo, Külli
author_facet Lättekivi, Freddy
Kõks, Sulev
Keermann, Maris
Reimann, Ene
Prans, Ele
Abram, Kristi
Silm, Helgi
Kõks, Gea
Kingo, Külli
author_sort Lättekivi, Freddy
collection PubMed
description Human endogenous retrovirus (HERV) sequences make up at least 8% of the human genome. Transcripts originating from these loci as well as proteins encoded by them have been detected in various tissues. HERVs are believed to be implicated in autoimmune diseases, however the extent to which, has remained unclear. Differential expression studies have so far been limited to certain HERV subfamilies with conserved sequences. No studies have been published describing the genome-wide expression pattern of HERVs and repetitive elements in the context of psoriasis. In the present study, we analysed total RNA sequencing data from skin samples of 12 psoriasis patients and 12 healthy controls, which enabled us to describe the entire transcriptional landscape of repetitive elements. We report high levels of repetitive element expression in the skin of psoriasis patients as well as healthy controls. The majority of differentially expressed elements were downregulated in lesional and non-lesional skin, suggesting active HERV suppression in the pro-inflammatory environment of psoriatic skin. However, we also report upregulation of a small subset of HERVs previously described in the context of autoimmune diseases, such as members of the HERV-K and W families, with the potential to affect the immunopathogenesis of psoriasis.
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spelling pubmed-58475432018-03-19 Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin Lättekivi, Freddy Kõks, Sulev Keermann, Maris Reimann, Ene Prans, Ele Abram, Kristi Silm, Helgi Kõks, Gea Kingo, Külli Sci Rep Article Human endogenous retrovirus (HERV) sequences make up at least 8% of the human genome. Transcripts originating from these loci as well as proteins encoded by them have been detected in various tissues. HERVs are believed to be implicated in autoimmune diseases, however the extent to which, has remained unclear. Differential expression studies have so far been limited to certain HERV subfamilies with conserved sequences. No studies have been published describing the genome-wide expression pattern of HERVs and repetitive elements in the context of psoriasis. In the present study, we analysed total RNA sequencing data from skin samples of 12 psoriasis patients and 12 healthy controls, which enabled us to describe the entire transcriptional landscape of repetitive elements. We report high levels of repetitive element expression in the skin of psoriasis patients as well as healthy controls. The majority of differentially expressed elements were downregulated in lesional and non-lesional skin, suggesting active HERV suppression in the pro-inflammatory environment of psoriatic skin. However, we also report upregulation of a small subset of HERVs previously described in the context of autoimmune diseases, such as members of the HERV-K and W families, with the potential to affect the immunopathogenesis of psoriasis. Nature Publishing Group UK 2018-03-12 /pmc/articles/PMC5847543/ /pubmed/29531256 http://dx.doi.org/10.1038/s41598-018-22734-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lättekivi, Freddy
Kõks, Sulev
Keermann, Maris
Reimann, Ene
Prans, Ele
Abram, Kristi
Silm, Helgi
Kõks, Gea
Kingo, Külli
Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin
title Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin
title_full Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin
title_fullStr Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin
title_full_unstemmed Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin
title_short Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin
title_sort transcriptional landscape of human endogenous retroviruses (hervs) and other repetitive elements in psoriatic skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847543/
https://www.ncbi.nlm.nih.gov/pubmed/29531256
http://dx.doi.org/10.1038/s41598-018-22734-7
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