Evidence map›Paper›PMID 28801535›Full record

ArticleEMBO reports2017

Expansion of the ISWI chromatin remodeler family with new active complexes.

Mariano Oppikofer, Tianyi Bai, Yutian Gan, Benjamin Haley, Peter Liu, Wendy Sandoval, Claudio Ciferri, Andrea G Cochran

Abstract read
In one paragraph

Article in EMBO reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
–field-weighted citation impact
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

69 citing papers in PubMed.

  1. Article
  2. BPTF is essential for vaccine-induced germinal center B cell responses.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. It Takes a Village of Chromatin Remodelers to Regulate rDNA Expression.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Review
  13. Professor Emma Whitelaw, a pioneer of epigenetic inheritance.Frontiers in epigenetics and epigenomics · 2025
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Mariano OppikoferDepartment of Early Discovery Biochemistry, Genentech, Inc., South San Francisco, CA, USA mariano.oppikofer@pfizer.com cochran.andrea@gene.com.ORCID 0000-0001-8579-0475
Tianyi BaiDepartment of Structural Biology, Genentech, Inc., South San Francisco, CA, USA.
Yutian GanDepartment of Protein Chemistry, Genentech, Inc., South San Francisco, CA, USA.
Benjamin HaleyDepartment of Molecular Biology, Genentech, Inc., South San Francisco, CA, USA.
Peter LiuDepartment of Protein Chemistry, Genentech, Inc., South San Francisco, CA, USA.
Wendy SandovalDepartment of Protein Chemistry, Genentech, Inc., South San Francisco, CA, USA.
Claudio CiferriDepartment of Structural Biology, Genentech, Inc., South San Francisco, CA, USA.
Andrea G CochranDepartment of Early Discovery Biochemistry, Genentech, Inc., South San Francisco, CA, USA mariano.oppikofer@pfizer.com cochran.andrea@gene.com.ORCID 0000-0001-6469-795X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ISWI chromatin remodelers mobilize nucleosomes to control DNA accessibility. Complexes isolated to date pair one of six regulatory subunits with one of two highly similar ATPases. However, we find that each endogenously expressed ATPase co-purifies with every regulatory subunit, substantially increasing the diversity of ISWI complexes, and we additionally identify BAZ2B as a novel, seventh regulatory subunit. Through reconstitution of catalytically active human ISWI complexes, we demonstrate that the new interactions described here are stable and direct. Finally, we profile the nucleosome remodeling functions of the now expanded family of ISWI chromatin remodelers. By revealing the combinatorial nature of ISWI complexes, we provide a basis for better understanding ISWI function in normal settings and disease.

Indexed as

Chromatin Assembly and DisassemblyAdenosine TriphosphatasesBromodomain Containing ProteinsChromatinChromosomal Proteins, Non-HistoneDNADNA-Binding ProteinsGene Expression RegulationHumansNucleosomesProtein BindingRNA-Binding ProteinsTranscription FactorsA1CF protein, humanAdenosine TriphosphatasesBAZ1A protein, humanBromodomain Containing ProteinsChromatinChromosomal Proteins, Non-HistoneDNADNA-Binding ProteinsISWI proteinNucleosomesRNA-Binding ProteinsSMARCA1 protein, humanTranscription FactorsACFBAZchromatin remodelersISWI ATPaseSMARCA

Identifiers

PMID28801535
PMCPMC5623870

What OpenQuestion holds

Textmetadata
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.