Human transposons are an abundant supply of transcription factor binding sites and promoter activities in breast cancer cell lines
Open Access
- 27 April 2019
- journal article
- research article
- Published by Springer Nature in Mobile DNA
- Vol. 10 (1) , 1-14
Abstract
Transposable elements (TE) are commonly regarded as “junk DNA” with no apparent regulatory roles in the human genome. However, a growing body of evidence demonstrates that some TEs exhibit regulatory activities in a range of biological pathways and diseases, with notable examples in bile metabolism and innate immunity. TEs are typically suppressed by epigenetic modifications in healthy somatic tissues, which prevents both undesirable effects of insertional mutagenesis, and also unwanted gene activation. Interestingly, TEs are widely reported to be dysregulated in epithelial cancers, and while much attention has been paid to their effects on genome instability, relatively little has been reported on their effects on gene regulation. Here, we investigated the contribution of TEs to the transcriptional regulation in breast cancer cell lines. We found that a subset of TE subfamilies were enriched in oncogenic transcription factor binding sites and also harboured histone marks associated with active transcription, raising the possibility of these subfamilies playing a broad role in breast cancer transcriptional regulation. To directly assess promoter activity in triple negative breast cancer cell lines, we identified four breast cancer-associated genes with putative TE-derived promoters. TE deletion confirmed a contribution to promoter activity in all cases, and for two examples the promoter activity was almost completely contained within the TE. Our findings demonstrate that TEs provide abundant oncogenic transcription factor binding sites in breast cancer and that individual TEs contain substantial promoter activity. Our findings provide further evidence for transcriptional regulation of human genes through TE exaptation by demonstrating the regulatory potential of TEs in multiple breast cancer cell lines.Keywords
Funding Information
- National Health and Medical Research Council (APP1130815)
This publication has 93 references indexed in Scilit:
- An integrated encyclopedia of DNA elements in the human genomeNature, 2012
- Characteristics of triple-negative breast cancerJournal of Cancer Research and Clinical Oncology, 2010
- The C/EBPbeta isoform, liver-inhibitory protein (LIP), induces autophagy in breast cancer cell linesExperimental Cell Research, 2010
- Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell IdentitiesMolecular Cell, 2010
- Changes in DNA methylation of tandem DNA repeats are different from interspersed repeats in cancerInternational Journal of Cancer, 2009
- High-Resolution Profiling of Histone Methylations in the Human GenomeCell, 2007
- Polycomb complexes repress developmental regulators in murine embryonic stem cellsNature, 2006
- Partitioning and Plasticity of Repressive Histone Methylation States in Mammalian ChromatinMolecular Cell, 2003
- Initial sequencing and analysis of the human genomeNature, 2001
- Selfish genes, the phenotype paradigm and genome evolutionNature, 1980