Evidence map›Paper›PMID 19308700›Full record

ReviewChromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology2009

Cohesin, gene expression and development: lessons from Drosophila.

Dale Dorsett

Open access · greenAbstract readReview
In one paragraph

Review in Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Downregulation of Cohesin Loading Factor Nipped-B-Like Protein (NIPBL) Induces Cell Cycle Arrest, Apoptosis, and Autophagy of Breast Cancer Cell Lines.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Using mouse and zebrafish models to understand the etiology of developmental defects in Cornelia de Lange Syndrome.American journal of medical genetics. Part C, Seminars in medical genetics · 2016
    Review
  12. Article
  13. Article
  14. Article
  15. SMC complexes link gene expression and genome architecture.Current opinion in genetics & development · 2014
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. RAD21 mutations cause a human cohesinopathy.American journal of human genetics · 2012
    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

1 author at 1 institution in 1 country.

Dale DorsettEdward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, 1100 South Grand Boulevard, Saint Louis, MO 63104, USA. dorsettd@slu.edu
Saint Louis University · US

Funding

VERTEBRATE ANIMAL MODELS OF CORNELIA DE LANGE SYNDROMEP01HD052860 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI KRANTZ, IAN D. · 2006 to 2015
$11.2M
LONG DISTANCE ENHANCER-PROMOTER INTERACTIONSR01GM055683 · NIGMS · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI DORSETT, DALE L · 1998 to 2012
$3.5M
NICHD NIH HHS P01 HD052860NIGMS NIH HHS R01 GM055683
6 · The paper itself

Abstract

The cohesin complex, discovered through its role in sister chromatid cohesion, also plays roles in gene expression and development in organisms from yeast to human. This review highlights what has been learned about the gene control and developmental functions of cohesin and the Nipped-B (NIPBL/Scc2) cohesin loading factor in Drosophila. The Drosophila studies have provided unique insights into the aetiology of Cornelia de Lange syndrome (CdLS), which is caused by mutations affecting sister chromatid cohesion proteins in humans. In vivo experiments with Drosophila show that cohesin and Nipped-B have dosage-sensitive effects on the functions of many evolutionarily conserved genes and developmental pathways. Genome-wide studies with Drosophila cultured cells show that Nipped-B and cohesin co-localize on chromosomes, and bind preferentially, but not exclusively, to many actively transcribed genes and their regulatory sequences, including many of the proposed in vivo target genes. In contrast, the cohesion factors are largely excluded from genes silenced by Polycomb group (PcG) proteins. Combined, the in vivo genetic data and the binding patterns of cohesin and Nipped-B in cultured cells are consistent with the hypothesis that they control the action of gene regulatory sequences, including transcriptional enhancers and insulators, and suggest that they might also help define active chromatin domains and influence transcriptional elongation.

Indexed as

Adenosine TriphosphatasesAnimalsCell Cycle ProteinsCells, CulturedChromatidsChromosomal Proteins, Non-HistoneChromosomesCohesinsDe Lange SyndromeDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsGene DosageGene Expression RegulationGene SilencingHumansAdenosine TriphosphatasesCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsDNA-Binding ProteinsDrosophila Proteinsnipped-B protein, DrosophilaPds5 protein, DrosophilaSMC3 protein, DrosophilaStructural Maintenance of Chromosome Protein 1

Identifiers

PMID19308700
PMCPMC2882070
OpenAlexW2043028159

What OpenQuestion holds

Textmetadata
LicenceTDM
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.