Evidence map›Paper›PMID 20696837›Full record

ReviewMolecular and cellular biology2010

Architectural epigenetics: mitotic retention of mammalian transcriptional regulatory information.

Sayyed K Zaidi, Daniel W Young, Martin Montecino, Jane B Lian, Janet L Stein, Andre J van Wijnen, Gary S Stein

Open access · greenAbstract readReview
In one paragraph

Review in Molecular and cellular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. A mixed modality approach towards Xi reactivation for Rett syndrome and other X-linked disorders.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Altered histone modifications in gliomas.Brain tumor research and treatment · 2014
    Review
  16. Article
  17. NFATc1 and NFATc2 repress spontaneous osteoarthritis.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  18. Article
  19. Article
  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

7 authors at 1 institution in 3 countries.

Sayyed K ZaidiDepartment of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Daniel W Young
Martin Montecino
Jane B Lian
Janet L Stein
Andre J van Wijnen
Gary S Stein
Universidad Andrés Bello · CL

Funding

SUBNUCLEAR TARGETING OF TRANSCRIPTION FACTORSP01CA082834 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, GARY S. · 2001 to 2015
$18.4M
PILOT AND FEASIBILITY PROGRAMP30DK032520 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI CZECH, MICHAEL P · 1986 to 2010
$14.6M
Subnuclear Integration of Regulatory Signals Controlling Bone Cell FunctionP01AR048818 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, JANET L · 2002 to 2011
$14.0M
Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
Synthesis of Osteocalcin in BoneR37DE012528 · NIDCR · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LIAN, JANE B. · 2008 to 2017
$5.0M
NCI NIH HHS P01 CA082834NIAMS NIH HHS P01 AR048818NIAMS NIH HHS R01 AR049069NIDCR NIH HHS 5R37 DE012528NIDCR NIH HHS R37 DE012528NIDDK NIH HHS 5 P30 DK32520NIDDK NIH HHS P30 DK032520
6 · The paper itself

Abstract

Epigenetic regulatory information must be retained during mammalian cell division to sustain phenotype-specific and physiologically responsive gene expression in the progeny cells. Histone modifications, DNA methylation, and RNA-mediated silencing are well-defined epigenetic mechanisms that control the cellular phenotype by regulating gene expression. Recent results suggest that the mitotic retention of nuclease hypersensitivity, selective histone marks, as well as the lineage-specific transcription factor occupancy of promoter elements contribute to the epigenetic control of sustained cellular identity in progeny cells. We propose that these mitotic epigenetic signatures collectively constitute architectural epigenetics, a novel and essential mechanism that conveys regulatory information to sustain the control of phenotype and proliferation in progeny cells by bookmarking genes for activation or suppression.

Indexed as

Epigenesis, GeneticAdenosine TriphosphatasesAnimalsCell DifferentiationCell ProliferationDNA-Binding ProteinsDNA MethylationGene Expression RegulationHistonesHumansMammalsMitosisModels, GeneticMultiprotein ComplexesPhenotypeProtein Processing, Post-TranslationalAdenosine Triphosphatasescondensin complexesDNA-Binding ProteinsHistonesMultiprotein ComplexesRNA, UntranslatedTranscription Factors

Identifiers

PMID20696837
PMCPMC2950539
OpenAlexW2147816015

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.