Evidence map›Paper›PMID 34475492›Full record

ArticleScientific reports2021

A prelude to the proximity interaction mapping of CXXC5.

Gamze Ayaz, Gizem Turan, Çağla Ece Olgun, Gizem Kars, Burcu Karakaya, Kerim Yavuz, Öykü Deniz Demiralay, Tolga Can, Mesut Muyan, Pelin Yaşar

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. CXXC5 is a ubiquitinated protein and is degraded by the ubiquitin-proteasome pathway.Protein science : a publication of the Protein Society · 2025
    Article
  3. Signal integrator function of CXXC5 in Cancer.Cell communication and signaling : CCS · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. 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

10 authors at 1 institution in 2 countries.

Gamze Ayaz *Department of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey. gamze.ayazsen@nih.gov.
Gizem Turan *Department of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Çağla Ece Olgun *Department of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Gizem KarsDepartment of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Burcu KarakayaDepartment of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Kerim YavuzDepartment of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Öykü Deniz DemiralayDepartment of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Tolga CanDepartment of Computer Engineering Middle, East Technical University, 06800, Ankara, Turkey.
Mesut MuyanDepartment of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey. mmuyan@metu.edu.tr.
Pelin Yaşar *Department of Biological Sciences, Middle East Technical University, 06800, Ankara, Turkey.
Middle East Technical University · TR

Funding

NCI NIH HHS HHSN261201400008CNCI NIH HHS HHSN261201500003CNCI NIH HHS HHSN261201500003I
6 · The paper itself

Abstract

CXXC5 is a member of the zinc-finger CXXC family proteins that interact with unmodified CpG dinucleotides through a conserved ZF-CXXC domain. CXXC5 is involved in the modulation of gene expressions that lead to alterations in diverse cellular events. However, the underlying mechanism of CXXC5-modulated gene expressions remains unclear. Proteins perform their functions in a network of proteins whose identities and amounts change spatiotemporally in response to various stimuli in a lineage-specific manner. Since CXXC5 lacks an intrinsic transcription regulatory function or enzymatic activity but is a DNA binder, CXXC5 by interacting with proteins could act as a scaffold to establish a chromatin state restrictive or permissive for transcription. To initially address this, we utilized the proximity-dependent biotinylation approach. Proximity interaction partners of CXXC5 include DNA and chromatin modifiers, transcription factors/co-regulators, and RNA processors. Of these, CXXC5 through its CXXC domain interacted with EMD, MAZ, and MeCP2. Furthermore, an interplay between CXXC5 and MeCP2 was critical for a subset of CXXC5 target gene expressions. It appears that CXXC5 may act as a nucleation factor in modulating gene expressions. Providing a prelude for CXXC5 actions, our results could also contribute to a better understanding of CXXC5-mediated cellular processes in physiology and pathophysiology.

Indexed as

Breast NeoplasmsDNA-Binding ProteinsFemaleHumansMCF-7 CellsMembrane ProteinsMethyl-CpG-Binding Protein 2Nuclear ProteinsProtein Interaction Domains and MotifsSignal TransductionTranscription Factorsc-MYC-associated zinc finger proteinCXXC5 protein, humanDNA-Binding ProteinsemerinMECP2 protein, humanMembrane ProteinsMethyl-CpG-Binding Protein 2Nuclear ProteinsTranscription Factors

Identifiers

PMID34475492
PMCPMC8413330
OpenAlexW3196313447

What Socratic 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 Socratic graph.