Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer

Abstract Tumor development involves alterations in DNA methylation patterns, which include both gains (hypermethylation) and losses (hypomethylation) in different genomic regions. The mechanisms underlying these two opposite, yet co-existing, alterations in tumors remain unclear. While studying the...

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Main Authors: Jean S. Fain, Axelle Loriot, Anna Diacofotaki, Aurélie Van Tongelen, Charles De Smet
Format: Article
Language:English
Published: Nature Portfolio 2021-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-96844-0
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author Jean S. Fain
Axelle Loriot
Anna Diacofotaki
Aurélie Van Tongelen
Charles De Smet
author_facet Jean S. Fain
Axelle Loriot
Anna Diacofotaki
Aurélie Van Tongelen
Charles De Smet
author_sort Jean S. Fain
collection DOAJ
description Abstract Tumor development involves alterations in DNA methylation patterns, which include both gains (hypermethylation) and losses (hypomethylation) in different genomic regions. The mechanisms underlying these two opposite, yet co-existing, alterations in tumors remain unclear. While studying the human MAGEA6/GABRA3 gene locus, we observed that DNA hypomethylation in tumor cells can lead to the activation of a long transcript (CT-GABRA3) that overlaps downstream promoters (GABRQ and GABRA3) and triggers their hypermethylation. Overlapped promoters displayed increases in H3K36me3, a histone mark deposited during transcriptional elongation and known to stimulate de novo DNA methylation. Consistent with such a processive mechanism, increases in H3K36me3 and DNA methylation were observed over the entire region covered by the CT-GABRA3 overlapping transcript. Importantly, experimental induction of CT-GABRA3 by depletion of DNMT1 DNA methyltransferase, resulted in a similar pattern of regional DNA hypermethylation. Bioinformatics analyses in lung cancer datasets identified other genomic loci displaying this process of coupled DNA hypo/hypermethylation, and some of these included tumor suppressor genes, e.g. RERG and PTPRO. Together, our work reveals that focal DNA hypomethylation in tumors can indirectly contribute to hypermethylation of nearby promoters through activation of overlapping transcription, and establishes therefore an unsuspected connection between these two opposite epigenetic alterations.
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spelling doaj.art-13c815e52ba34a6ab5ae1ab31236669e2022-12-21T22:56:52ZengNature PortfolioScientific Reports2045-23222021-08-0111111410.1038/s41598-021-96844-0Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancerJean S. Fain0Axelle Loriot1Anna Diacofotaki2Aurélie Van Tongelen3Charles De Smet4Group of Genetics and Epigenetics, de Duve Institute, Université Catholique de LouvainGroup of Genetics and Epigenetics, de Duve Institute, Université Catholique de LouvainGroup of Genetics and Epigenetics, de Duve Institute, Université Catholique de LouvainGroup of Genetics and Epigenetics, de Duve Institute, Université Catholique de LouvainGroup of Genetics and Epigenetics, de Duve Institute, Université Catholique de LouvainAbstract Tumor development involves alterations in DNA methylation patterns, which include both gains (hypermethylation) and losses (hypomethylation) in different genomic regions. The mechanisms underlying these two opposite, yet co-existing, alterations in tumors remain unclear. While studying the human MAGEA6/GABRA3 gene locus, we observed that DNA hypomethylation in tumor cells can lead to the activation of a long transcript (CT-GABRA3) that overlaps downstream promoters (GABRQ and GABRA3) and triggers their hypermethylation. Overlapped promoters displayed increases in H3K36me3, a histone mark deposited during transcriptional elongation and known to stimulate de novo DNA methylation. Consistent with such a processive mechanism, increases in H3K36me3 and DNA methylation were observed over the entire region covered by the CT-GABRA3 overlapping transcript. Importantly, experimental induction of CT-GABRA3 by depletion of DNMT1 DNA methyltransferase, resulted in a similar pattern of regional DNA hypermethylation. Bioinformatics analyses in lung cancer datasets identified other genomic loci displaying this process of coupled DNA hypo/hypermethylation, and some of these included tumor suppressor genes, e.g. RERG and PTPRO. Together, our work reveals that focal DNA hypomethylation in tumors can indirectly contribute to hypermethylation of nearby promoters through activation of overlapping transcription, and establishes therefore an unsuspected connection between these two opposite epigenetic alterations.https://doi.org/10.1038/s41598-021-96844-0
spellingShingle Jean S. Fain
Axelle Loriot
Anna Diacofotaki
Aurélie Van Tongelen
Charles De Smet
Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer
Scientific Reports
title Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer
title_full Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer
title_fullStr Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer
title_full_unstemmed Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer
title_short Transcriptional overlap links DNA hypomethylation with DNA hypermethylation at adjacent promoters in cancer
title_sort transcriptional overlap links dna hypomethylation with dna hypermethylation at adjacent promoters in cancer
url https://doi.org/10.1038/s41598-021-96844-0
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