Evidence map›Paper›PMID 22807655›Full record

ArticlePLoS biology2012

Regulation of DNA replication within the immunoglobulin heavy-chain locus during B cell commitment.

Agnieszka Demczuk, Michel G Gauthier, Ingrid Veras, Settapong Kosiyatrakul, Carl L Schildkraut, Meinrad Busslinger, John Bechhoefer, Paolo Norio

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Super-resolution microscopy reveals stochastic initiation of replication in Drosophila polytene chromosomes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Mammalian DNA Replication Timing.Cold Spring Harbor perspectives in biology · 2021
    Review
  12. Article
  13. NAR genomics and bioinformatics · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Control of DNA replication timing in the 3D genome.Nature reviews. Molecular cell biology · 2019
    Review
  18. Article
  19. Review
  20. Review
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 3 countries.

Agnieszka DemczukDepartment of Oncology, Montefiore Medical Center, Moses Division, Bronx, New York, USA.
Michel G Gauthier
Ingrid Veras
Settapong Kosiyatrakul
Carl L Schildkraut
Meinrad Busslinger
John Bechhoefer
Paolo Norio
Montefiore Medical Center · USAlbert Einstein College of Medicine · USSimon Fraser University · CAResearch Institute of Molecular Pathology · AT

Funding

DNA REPLICATION INITIATION SITES IN MAMMALIAN CELLSR01GM045751 · NIGMS · YESHIVA UNIVERSITY · PI SCHILDKRAUT, CARL L · 1992 to 2023
$13.4M
Molecular basis of Replication origin activation/silecing during tissue-specificR01GM080606 · NIGMS · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI NORIO, PAOLO · 2007 to 2011
$1.3M
NIGMS NIH HHS R01 GM045751NIGMS NIH HHS R01GM045751NIGMS NIH HHS R01 GM080606NIGMS NIH HHS R01GM080606
6 · The paper itself

Abstract

The temporal order of replication of mammalian chromosomes appears to be linked to their functional organization, but the process that establishes and modifies this order during cell differentiation remains largely unknown. Here, we studied how the replication of the Igh locus initiates, progresses, and terminates in bone marrow pro-B cells undergoing B cell commitment. We show that many aspects of DNA replication can be quantitatively explained by a mechanism involving the stochastic firing of origins (across the S phase and the Igh locus) and extensive variations in their firing rate (along the locus). The firing rate of origins shows a high degree of coordination across Igh domains that span tens to hundreds of kilobases, a phenomenon not observed in simple eukaryotes. Differences in domain sizes and firing rates determine the temporal order of replication. During B cell commitment, the expression of the B-cell-specific factor Pax5 sharply alters the temporal order of replication by modifying the rate of origin firing within various Igh domains (particularly those containing Pax5 binding sites). We propose that, within the Igh C(H)-3'RR domain, Pax5 is responsible for both establishing and maintaining high rates of origin firing, mostly by controlling events downstream of the assembly of pre-replication complexes.

Indexed as

DNA ReplicationAnimalsBinding SitesB-LymphocytesCell LineageHumansImmunoglobulin Heavy ChainsMicePAX5 Transcription FactorStochastic ProcessesImmunoglobulin Heavy ChainsPAX5 protein, humanPAX5 Transcription Factor

Identifiers

PMID22807655
PMCPMC3393677
OpenAlexW2169114939

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.