scTEM-seq: Single-cell analysis of transposable element methylation to link global epigenetic heterogeneity with transcriptional programs

Bibliographic Details
Title: scTEM-seq: Single-cell analysis of transposable element methylation to link global epigenetic heterogeneity with transcriptional programs
Authors: Kooper V. Hunt, Sean M. Burnard, Ellise A. Roper, Danielle R. Bond, Matthew D. Dun, Nicole M. Verrills, Anoop K. Enjeti, Heather J. Lee
Source: Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Publisher Information: Nature Portfolio, 2022.
Publication Year: 2022
Collection: LCC:Medicine
LCC:Science
Subject Terms: Medicine, Science
More Details: Abstract Global changes in DNA methylation are observed in development and disease, and single-cell analyses are highlighting the heterogeneous regulation of these processes. However, technical challenges associated with single-cell analysis of DNA methylation limit these studies. We present single-cell transposable element methylation sequencing (scTEM-seq) for cost-effective estimation of average DNA methylation levels. By targeting high-copy SINE Alu elements, we achieve amplicon bisulphite sequencing with thousands of loci covered in each scTEM-seq library. Parallel transcriptome analysis is also performed to link global DNA methylation estimates with gene expression. We apply scTEM-seq to KG1a acute myeloid leukaemia (AML) cells, and primary AML cells. Our method reveals global DNA methylation heterogeneity induced by decitabine treatment of KG1a cells associated with altered expression of immune process genes. We also compare global DNA methylation estimates to expression of transposable elements and find a predominance of negative correlations. Finally, we observe co-ordinated upregulation of many transposable elements in a sub-set of decitabine treated cells. By linking global DNA methylation heterogeneity with transcription, scTEM-seq will refine our understanding of epigenetic regulation in cancer and beyond.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2045-2322
73119636
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-022-09765-x
Access URL: https://doaj.org/article/73119636505547c88c866348273eac38
Accession Number: edsdoj.73119636505547c88c866348273eac38
Database: Directory of Open Access Journals
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More Details
ISSN:20452322
73119636
DOI:10.1038/s41598-022-09765-x
Published in:Scientific Reports
Language:English