CTCF regulates the human p53 gene through direct interaction with its natural antisense transcript, Wrap53
Open accessAbstract
The multifunctional CCCTC-binding factor (CTCF) protein exhibits a broad range of functions, including that of insulator and higher-order chromatin organizer. We found that CTCF comprises a previously unrecognized region that is necessary and sufficient to bind RNA (RNA-binding region [RBR]) and is distinct from its DNA-binding domain. Depletion of cellular CTCF led to a decrease in not only levels of p53 mRNA, as expected, but also those of Wrap53 RNA, an antisense transcript originated from the p53 locus. PAR-CLIP-seq (photoactivatable ribonucleoside-enhanced cross-linking and immunoprecipitation [PAR-CLIP] combined with deep sequencing) analyses indicate that CTCF binds a multitude of transcripts genome-wide as well as to Wrap53 RNA. Apart from its established role at the p53 promoter, CTCF regulates p53 expression through its physical interaction with Wrap53 RNA. Cells harboring a CTCF mutant in its RBR exhibit a defective p53 response to DNA damage. Moreover, the RBR facilitates CTCF multimerization in an RNA-dependent manner, which may bear directly on its role in establishing higher-order chromatin structures in vivo.
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Non-coding RNA has been implicated in regulation of CTCF binding to DNA at certain loci.
“Non-coding RNA has also been implicated in regulation of CTCF binding to DNA at certain loci (Saldana-Meyer et al., 2014).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Saldana-Meyer et al., 2014
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References 38 · Cited by 217
- Authors
- Saldaña-Meyer, R., González-Buendía, E., Guerrero, G., Narendra, V., Bonasio, R., Recillas-Targa, F., & Reinberg, D.
- Affiliations
- Universidad Nacional Autónoma de México (MX)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Reinberg, Danny
- ORCID
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2014-04-01
- Volume
- 28
- Issue
- 7
- Pages
- 723-734
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC4015496
- OpenAlex
- W2136603536
- Cited by
- 217
- References
- 38
- Citations by year
- 2026: 6 · 2025: 10 · 2024: 26 · 2023: 18 · 2022: 16 · 2021: 19 · 2020: 22 · 2019: 25 · 2018: 17 · 2017: 20 · 2016: 16 · 2015: 16 · 2014: 6
- Type
- posted content
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- Genes & Development (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- York University
- National Institutes of Health (R37-37120)
- U.S. Public Health Service (R37-37120)
- National Cancer Institute (P30CA016087)
- National Institute of General Medical Sciences (GM 64844, T32GM007308, T32GM007238, R01GM064844)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Keywords
- CTCF, p53, WRAP53, antisense transcripts, RNA-binding domain, RNA-binding proteins, DNA damage response, chromatin organization, PAR-CLIP
- MeSH terms
- CCCTC-Binding Factor, DNA Damage, Gene Expression Regulation, Humans, Mutation, Protein Binding, Repressor Proteins, RNA, Genes, p53, Sequence Deletion, Molecular Chaperones, Telomerase, Cell Line, Tumor, Protein Multimerization
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