Transcription factor trapping by RNA in gene regulatory elements
Open accessAbstract
Noncoding RNA helps protein binding: Besides reading the coding regions of genes, RNA polymerase generates RNA at promoter-proximal and -distal DNA elements, but the function of these molecules is largely unknown. Sigova et al. show that these RNAs facilitate interactions between gene regulators and the regulatory elements they occupy. Nascent RNA associates with the transcription factor YY1 and increases its ability to bind DNA. Thus, transcription at active regulatory elements may provide a positive feedback loop that reinforces regulatory elements contributing to the stability of gene expression programs. Science , this issue p. 978
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eRNA can capture various transcription factors, thereby increasing their local concentration on the enhancer.
“In addition, eRNA can capture various transcription factors [65], thereby increasing their local concentration on the enhancer.”
From Enhancer Function in the 3D Genome (2023) · cites this paper as [65]
The passages labeled Abstract (page not provided) report that RNA tethered near enhancers increases YY1 occupancy and propose that nascent RNA traps dissociating YY1. The paper suggests other transcription factors may behave similarly, but it does not establish that enhancer RNA captures various transcription factors. (LLM, conf=0.86)
Experimental — accuracy not yet measuredCurrent theories propose liquid-liquid phase separation and some form of transcription factor trapping or engagement of transcription factors in multivalent interactions independent of assembly into phase-separated liquid-like droplets.
“current theories propose liquid-liquid phase separation18,64–66 and some form of TF trapping22,67 or engagement of TFs in multivalent interactions independent of assembly into phase-separated liquid-like droplets.68”
From Super-enhancers include classical enhancers and facilitators to fully activate gene expression (2023) · cites this paper as [67]
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- Authors
- Sigova, A. A., Abraham, B. J., Ji, X., Molinie, B., Hannett, N. M., Guo, Y. E., Jangi, M., Giallourakis, C. C., Sharp, P. A., & Young, R. A.
- Affiliations
- Whitehead Institute for Biomedical Research (US)
- Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
- Koch Institute for Integrative Cancer Research At MIT (US)
- Harvard University (US)
- Corresponding author
- Young, Richard A.
- Venue
- Science
- Published
- 2015-11-20
- Volume
- 350
- Issue
- 6263
- Pages
- 978-981
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4720525
- OpenAlex
- W2618657542
- Cited by
- 492
- References
- 9
- Citations by year
- 2026: 18 · 2025: 30 · 2024: 62 · 2023: 55 · 2022: 52 · 2021: 53 · 2020: 52 · 2019: 39 · 2018: 44 · 2017: 42 · 2016: 44 · 2015: 1
- FWCI
- 18.97
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion)
- Funders
- NIH (HG002668)
- Cancer Research Institute
- Biogen
- Hope Funds for Cancer Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- RNA transcription, gene regulatory elements, distal regulatory elements, YY1, transcription factor occupancy, positive feedback loop, gene expression stability, transcriptional regulation
- MeSH terms
- Animals, Base Sequence, Binding Sites, Cell Line, DNA, Enhancer Elements, Genetic, Gene Expression Regulation, Promoter Regions, Genetic, RNA, Messenger, Transcription, Genetic, Consensus Sequence, YY1 Transcription Factor, Mice, Embryonic Stem Cells
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