Evidence map›Paper›PMID 14767778›Full record

ArticleChromosoma2004

A high proportion of genes involved in position effect variegation also affect chromosome inheritance.

Hiep D Le, Kathryn M Donaldson, Kevin R Cook, Gary H Karpen

Open access · greenAbstract read
In one paragraph

Article in Chromosoma, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. The role of SUMOylation during development.Biochemical Society transactions · 2020
    Review
  2. Article
  3. Article
  4. Article
  5. Diverse factors are involved in maintaining X chromosome inactivation.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  6. Article
  7. Review
  8. 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

4 authors at 2 institutions in 1 country.

Hiep D LeDepartment of Genome Sciences, Lawrence Berkeley National Laboratory, One Cyclotron Road, MS-84R0171, Berkeley, CA 94720, USA.
Kathryn M Donaldson
Kevin R Cook
Gary H Karpen
Lawrence Berkeley National Laboratory · USIndiana University · US

Funding

Salk Institute Cancer Training GrantT32CA009370 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Diana Clare Hargreaves, Jan Karlseder · 1986 to 2026
$8.6M
Determinants of Centromere Identity in DrosophilaR01GM066272 · NIGMS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI KARPEN, GARY H · 2004 to 2011
$3.4M
DROSOPHILA CENTROMERE PROTEIN GENESR01GM054549 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI KARPEN, GARY H. · 1996 to 2000
$82k
NCI NIH HHS CA-09370NCI NIH HHS T32 CA009370NIGMS NIH HHS R01 GM066272NIGMS NIH HHS R01 GM 54549
6 · The paper itself

Abstract

Suppressors and enhancers of position effect variegation (PEV) have been linked to the establishment and maintenance of heterochromatin. The presence of centromeres and other inheritance elements in heterochromatic regions suggests that suppressors and enhancers of PEV, Su(var) s and E(var)s [collectively termed Mod(var)s], may be required for chromosome inheritance. In order to test this hypothesis, we screened 59 ethyl methanesulfonate-generated Drosophila Mod(var)s for dominant effects on the partially compromised inheritance of a minichromosome ( J21A) missing a portion of the genetically defined centromere. Nearly half of these Mod(var)s significantly increased or decreased the transmission of J21A. Analyses of homozygous mutant larval neuroblasts suggest that these mutations affect cell cycle progression and native chromosome morphology. Five out of six complementation groups tested displayed mitotic abnormalities, including phenotypes such as telomere fusions, overcondensed chromosomes, and low mitotic index. We conclude that Mod(var)s as a group are highly enriched for genes that encode essential inheritance functions. We propose that a primary function of Mod(var)s is to promote chromosome inheritance, and that the gene silencing phenotype associated with PEV may be a secondary consequence of the heterochromatic structures required to carry out these functions.

Indexed as

Genes, InsectAnimalsCell CycleCentromereDisease Transmission, InfectiousDrosophila melanogasterEthyl MethanesulfonateFemaleGenes, DominantGene SilencingGenetic Complementation TestHeterochromatinHomozygoteLarvaMaleMitotic IndexEthyl MethanesulfonateHeterochromatin

Identifiers

PMID14767778
PMCPMC3116012
OpenAlexW2040118603

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.