Evidence map›Paper›PMID 30676316›Full record

ArticleeLife2019

Exploration of CTCF post-translation modifications uncovers Serine-224 phosphorylation by PLK1 at pericentric regions during the G2/M transition.

Brian C Del Rosario, Andrea J Kriz, Amanda M Del Rosario, Anthony Anselmo, Christopher J Fry, Forest M White, Ruslan I Sadreyev, Jeannie T Lee

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Re-establishment of TAD boundary organization during DNA replication.bioRxiv : the preprint server for biology · 2026
    Article
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  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. CTCF: A misguided jack-of-all-trades in cancer cells.Computational and structural biotechnology journal · 2022
    Review
  15. Article
  16. Article
  17. Regulation of 3D chromatin organization by CTCF.Current opinion in genetics & development · 2021
    Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Brian C Del Rosario *Department of Molecular Biology, Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, United States.ORCID 0000-0002-9976-1541
Andrea J Kriz *Department of Molecular Biology, Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, United States.ORCID 0000-0002-3395-4498
Amanda M Del RosarioKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, United States.
Anthony AnselmoDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Christopher J FryCell Signaling Technology, Danvers, United States.
Forest M WhiteKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, United States.
Ruslan I SadreyevDepartment of Molecular Biology, Massachusetts General Hospital, Boston, United States.
Jeannie T LeeDepartment of Molecular Biology, Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, United States.ORCID 0000-0001-7786-8850
Howard Hughes Medical Institute · USMassachusetts General Hospital · USMassachusetts Institute of Technology · USCell Signaling Technology (United States) · US

Funding

ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER P DUGGAN · 1994 to 2026
$31.6M
Regulation of X-Inactivation by Non-Coding RNA LociR01GM058839 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, JEANNIE T · 1999 to 2025
$6.7M
Regulation of X-chromosome Inactivation and Imprinting by Non-coding ElementsR37GM058839 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI LEE, JEANNIE T · 2012 to 2021
$4.1M
Herchel Smith Endowment fund Herchel Smith Graduate FellowshipNational Science Foundation NSF GRFPNIDDK NIH HHS P30 DK040561NIGMS NIH HHS R01 GM058839NIGMS NIH HHS R37 GM058839NIH HHS R37-GM58839
6 · The paper itself

Abstract

The zinc finger CCCTC-binding protein (CTCF) carries out many functions in the cell. Although previous studies sought to explain CTCF multivalency based on sequence composition of binding sites, few examined how CTCF post-translational modification (PTM) could contribute to function. Here, we performed CTCF mass spectrometry, identified a novel phosphorylation site at Serine 224 (Ser

Indexed as

G2 PhaseMitosisProtein Processing, Post-TranslationalAmino Acid SequenceAnimalsBase SequenceCasein Kinase IICCCTC-Binding FactorCell Cycle ProteinsCell ProliferationChromatinConserved SequenceDNADNA Mutational AnalysisHumansInterphaseCasein Kinase IICCCTC-Binding FactorCell Cycle ProteinsChromatinDNAMembrane ProteinsPhosphoserinePolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsRNATumor Suppressor Protein p53cell cyclechromosome architecturechromosomesCTCFgene expressionmousePLK1post-translational modification

Identifiers

PMID30676316
PMCPMC6361588
OpenAlexW2914051711

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.