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Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements

BACKGROUND: Despite the long-held assumption that transposons are normally only expressed in the germ-line, recent evidence shows that transcripts of transposable element (TE) sequences are frequently found in the somatic cells. However, the extent of variation in TE transcript levels across differe...

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Autores principales: Chung, Nicky, Jonaid, G. M., Quinton, Sophia, Ross, Austin, Sexton, Corinne E., Alberto, Adrian, Clymer, Cody, Churchill, Daphnie, Navarro Leija, Omar, Han, Mira V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720085/
https://www.ncbi.nlm.nih.gov/pubmed/31497073
http://dx.doi.org/10.1186/s13100-019-0180-5
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author Chung, Nicky
Jonaid, G. M.
Quinton, Sophia
Ross, Austin
Sexton, Corinne E.
Alberto, Adrian
Clymer, Cody
Churchill, Daphnie
Navarro Leija, Omar
Han, Mira V.
author_facet Chung, Nicky
Jonaid, G. M.
Quinton, Sophia
Ross, Austin
Sexton, Corinne E.
Alberto, Adrian
Clymer, Cody
Churchill, Daphnie
Navarro Leija, Omar
Han, Mira V.
author_sort Chung, Nicky
collection PubMed
description BACKGROUND: Despite the long-held assumption that transposons are normally only expressed in the germ-line, recent evidence shows that transcripts of transposable element (TE) sequences are frequently found in the somatic cells. However, the extent of variation in TE transcript levels across different tissues and different individuals are unknown, and the co-expression between TEs and host gene mRNAs have not been examined. RESULTS: Here we report the variation in TE derived transcript levels across tissues and between individuals observed in the non-tumorous tissues collected for The Cancer Genome Atlas. We found core TE co-expression modules consisting mainly of transposons, showing correlated expression across broad classes of TEs. Despite this co-expression within tissues, there are individual TE loci that exhibit tissue-specific expression patterns, when compared across tissues. The core TE modules were negatively correlated with other gene modules that consisted of immune response genes in interferon signaling. KRAB Zinc Finger Proteins (KZFPs) were over-represented gene members of the TE modules, showing positive correlation across multiple tissues. But we did not find overlap between TE-KZFP pairs that are co-expressed and TE-KZFP pairs that are bound in published ChIP-seq studies. CONCLUSIONS: We find unexpected variation in TE derived transcripts, within and across non-tumorous tissues. We describe a broad view of the RNA state for non-tumorous tissues exhibiting higher level of TE transcripts. Tissues with higher level of TE transcripts have a broad range of TEs co-expressed, with high expression of a large number of KZFPs, and lower RNA levels of immune genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13100-019-0180-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-67200852019-09-06 Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements Chung, Nicky Jonaid, G. M. Quinton, Sophia Ross, Austin Sexton, Corinne E. Alberto, Adrian Clymer, Cody Churchill, Daphnie Navarro Leija, Omar Han, Mira V. Mob DNA Research BACKGROUND: Despite the long-held assumption that transposons are normally only expressed in the germ-line, recent evidence shows that transcripts of transposable element (TE) sequences are frequently found in the somatic cells. However, the extent of variation in TE transcript levels across different tissues and different individuals are unknown, and the co-expression between TEs and host gene mRNAs have not been examined. RESULTS: Here we report the variation in TE derived transcript levels across tissues and between individuals observed in the non-tumorous tissues collected for The Cancer Genome Atlas. We found core TE co-expression modules consisting mainly of transposons, showing correlated expression across broad classes of TEs. Despite this co-expression within tissues, there are individual TE loci that exhibit tissue-specific expression patterns, when compared across tissues. The core TE modules were negatively correlated with other gene modules that consisted of immune response genes in interferon signaling. KRAB Zinc Finger Proteins (KZFPs) were over-represented gene members of the TE modules, showing positive correlation across multiple tissues. But we did not find overlap between TE-KZFP pairs that are co-expressed and TE-KZFP pairs that are bound in published ChIP-seq studies. CONCLUSIONS: We find unexpected variation in TE derived transcripts, within and across non-tumorous tissues. We describe a broad view of the RNA state for non-tumorous tissues exhibiting higher level of TE transcripts. Tissues with higher level of TE transcripts have a broad range of TEs co-expressed, with high expression of a large number of KZFPs, and lower RNA levels of immune genes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13100-019-0180-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-03 /pmc/articles/PMC6720085/ /pubmed/31497073 http://dx.doi.org/10.1186/s13100-019-0180-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Chung, Nicky
Jonaid, G. M.
Quinton, Sophia
Ross, Austin
Sexton, Corinne E.
Alberto, Adrian
Clymer, Cody
Churchill, Daphnie
Navarro Leija, Omar
Han, Mira V.
Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
title Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
title_full Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
title_fullStr Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
title_full_unstemmed Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
title_short Transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
title_sort transcriptome analyses of tumor-adjacent somatic tissues reveal genes co-expressed with transposable elements
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720085/
https://www.ncbi.nlm.nih.gov/pubmed/31497073
http://dx.doi.org/10.1186/s13100-019-0180-5
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