PreprintCited by 217Genomics and Chromatin DynamicsCancer-related molecular mechanisms researchCancer-related Molecular Pathways

CTCF regulates the human p53 gene through direct interaction with its natural antisense transcript, Wrap53

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Saldaña-Meyer, Ricardo, González-Buendía, Edgar, Guerrero, Georgina, Narendra, Varun, Bonasio, Roberto, Recillas-Targa, Félix, Reinberg, Danny·2014·Genes & Development

Abstract

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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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
Venue
Genes & Development
Published
2014-04-01
Volume
28
Issue
7
Pages
723-734
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
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
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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