Evidence map›Paper›PMID 36717582›Full record

ArticleNature communications2023

B1 SINE-binding ZFP266 impedes mouse iPSC generation through suppression of chromatin opening mediated by reprogramming factors.

Daniel F Kaemena, Masahito Yoshihara, Meryam Beniazza, James Ashmore, Suling Zhao, Mårten Bertenstam, Victor Olariu, Shintaro Katayama, Keisuke Okita, Simon R Tomlinson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Cell reprogramming: methods, mechanisms and applications.Cell regeneration (London, England) · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. 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

12 authors at 5 institutions in 4 countries.

Daniel F KaemenaCentre for Regenerative Medicine, Institute for Regenaration and Repair, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh, Scotland, UK.
Masahito YoshiharaDepartment of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-8915-9282
Meryam BeniazzaCentre for Regenerative Medicine, Institute for Regenaration and Repair, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh, Scotland, UK.
James AshmoreCentre for Regenerative Medicine, Institute for Regenaration and Repair, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh, Scotland, UK.
Suling ZhaoCentre for Regenerative Medicine, Institute for Regenaration and Repair, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh, Scotland, UK.
Mårten BertenstamComputational Biology and Biological Physics, Lund University, Lund, Sweden.
Victor OlariuComputational Biology and Biological Physics, Lund University, Lund, Sweden.
Shintaro KatayamaDepartment of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-7581-5157
Keisuke OkitaCenter for iPS Cell Research and Application, Kyoto University, Kyoto, Japan.ORCID 0000-0001-5806-1090
Simon R TomlinsonCentre for Regenerative Medicine, Institute for Regenaration and Repair, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh, Scotland, UK.
Kosuke YusaStem Cell Genetics, Wellcome Sanger Institute, Hinxton, Cambridge, UK.ORCID 0000-0002-3442-021X
Keisuke KajiCentre for Regenerative Medicine, Institute for Regenaration and Repair, University of Edinburgh, Edinburgh BioQuarter, 5 Little France Drive, Edinburgh, Scotland, UK. keisuke.kaji@ed.ac.uk.ORCID 0000-0001-5946-8415
MRC Centre for Regenerative Medicine · GBKyoto University · JPLund University · SEChiba University · JPKarolinska Institutet · SE

Funding

Medical Research Council MR/N008715/1Wellcome Trust
6 · The paper itself

Abstract

Induced pluripotent stem cell (iPSC) reprogramming is inefficient and understanding the molecular mechanisms underlying this inefficiency holds the key to successfully control cellular identity. Here, we report 24 reprogramming roadblock genes identified by CRISPR/Cas9-mediated genome-wide knockout (KO) screening. Of these, depletion of the predicted KRAB zinc finger protein (KRAB-ZFP) Zfp266 strongly and consistently enhances murine iPSC generation in several reprogramming settings, emerging as the most robust roadblock. We show that ZFP266 binds Short Interspersed Nuclear Elements (SINEs) adjacent to binding sites of pioneering factors, OCT4 (POU5F1), SOX2, and KLF4, and impedes chromatin opening. Replacing the KRAB co-suppressor with co-activator domains converts ZFP266 from an inhibitor to a potent facilitator of iPSC reprogramming. We propose that the SINE-KRAB-ZFP interaction is a critical regulator of chromatin accessibility at regulatory elements required for efficient cellular identity changes. In addition, this work serves as a resource to further illuminate molecular mechanisms hindering reprogramming.

Indexed as

Induced Pluripotent Stem CellsZinc FingersAnimalsCellular ReprogrammingChromatinKruppel-Like Factor 4MiceChromatinKruppel-Like Factor 4

Identifiers

PMID36717582
PMCPMC9887000
OpenAlexW4318482116

What OpenQuestion holds

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LicenceCC BY
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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.