Regulatory transposable elements in the encyclopedia of DNA elements

Transposable elements (TEs) comprise ~50% of our genome, but knowledge of how TEs affect genome evolution remains incomplete. Leveraging ENCODE4 data, we provide the most comprehensive study to date of TE contributions to the regulatory genome. We find 236,181 (~25%) human candidate cis-regulatory elements (cCREs) are TE-derived, with over 90% lineage-specific since the human-mouse split, accounting for 8-36% of lineage-specific cCREs. Except for SINEs, cCRE-associated transcription factor (TF) motifs in TEs are derived from ancestral TE sequence more than expected by chance. We show that TEs may adopt similar regulatory activities of elements near their integration site. Since human-mouse divergence, TEs have contributed 3-56% of TF binding site turnover events across 30 examined TFs. Finally, TE-derived cCREs are similar to non-TE cCREs in terms of MPRA activity and GWAS variant enrichment. Overall, our results substantiate the notion that TEs have played an important role in shaping the human regulatory genome.

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Publication Details

Journal
Nature Communications
Published
2024-08-31
DOI
https://doi.org/10.1038/s41467-024-51921-6
Citations
43
Primary Topic
Chromosomal and Genetic Variations
Type
article
Field-Weighted Citation Impact
25.18

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article

Regulatory transposable elements in the encyclopedia of DNA elements

Xiaoyu Zhuo, Jason D. Chobirko, Cédric Feschotte, Alan Y. Du et al.
43 citations
Nature Communications
Chromosomal and Genetic Variations
25.18
article

Regulatory transposable elements in the encyclopedia of DNA elements

Xiaoyu Zhuo, Jason D. Chobirko, Cédric Feschotte, Alan Y. Du, Ting Wang
article en
43 citations

Abstract

Transposable elements (TEs) comprise ~50% of our genome, but knowledge of how TEs affect genome evolution remains incomplete. Leveraging ENCODE4 data, we provide the most comprehensive study to date of TE contributions to the regulatory genome. We find 236,181 (~25%) human candidate cis-regulatory elements (cCREs) are TE-derived, with over 90% lineage-specific since the human-mouse split, accounting for 8-36% of lineage-specific cCREs. Except for SINEs, cCRE-associated transcription factor (TF) motifs in TEs are derived from ancestral TE sequence more than expected by chance. We show that TEs may adopt similar regulatory activities of elements near their integration site. Since human-mouse divergence, TEs have contributed 3-56% of TF binding site turnover events across 30 examined TFs. Finally, TE-derived cCREs are similar to non-TE cCREs in terms of MPRA activity and GWAS variant enrichment. Overall, our results substantiate the notion that TEs have played an important role in shaping the human regulatory genome.

Nature CommunicationsVol. 15(1)
James S. McDonnell Foundation (US), Washington University in St. Louis (US), Cornell University (US), Living Systems (United States) (US)
National Institutes of Health, National Human Genome Research Institute, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 0%
Chromosomal and Genetic Variations
25.18
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Regulatory transposable elements in the encyclopedia of DNA elements — Xiaoyu Zhuo, Jason D. Chobirko, et al. · Nature Communications (2024) | TGRS Research Map | TGRS