Evidence map›Paper›PMID 11533234›Full record

ArticleMolecular and cellular biology2001

Widespread collaboration of Isw2 and Sin3-Rpd3 chromatin remodeling complexes in transcriptional repression.

T G Fazzio, C Kooperberg, J P Goldmark, C Neal, R Basom, J Delrow, T Tsukiyama

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

99 citing papers in PubMed, 205 citations in OpenAlex.

  1. Article
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  3. Microorganisms · 2022
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  5. Review
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  18. Crawling wounded: molecular genetic insights into wound healing from Drosophila larvae.The International journal of developmental biology · 2018
    Review
  19. Article
  20. Sequence-specific targeting of chromatin remodelers organizes precisely positioned nucleosomes throughout the genome.BioEssays : news and reviews in molecular, cellular and developmental biology · 2017
    Review

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

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 3 institutions in 2 countries.

T G FazzioDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.
C Kooperberg
J P Goldmark
C Neal
R Basom
J Delrow
T Tsukiyama
Office of Basic Energy Sciences · USFaculty of Public Health · GBUniversity of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Molecular analysis of yeast lsw1 and lsw2 complexesR01GM058465 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TSUKIYAMA, TOSHIO · 1999 to 2019
$9.2M
Adaptive Function Estimation for Genomic DataR01CA074841 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2003 to 2006
$1.1M
HAZARD REGRESSION AND OTHER POLYNOMIAL SPLINE METHODSR29CA074841 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 1998 to 2002
$351k
NCI NIH HHS 5P30 CA15704-28NCI NIH HHS CA74841NCI NIH HHS P30 CA015704NCI NIH HHS R01 CA074841NCI NIH HHS R29 CA074841NIGMS NIH HHS GM58465NIGMS NIH HHS R01 GM058465
6 · The paper itself

Abstract

The yeast Isw2 chromatin remodeling complex functions in parallel with the Sin3-Rpd3 histone deacetylase complex to repress early meiotic genes upon recruitment by Ume6p. For many of these genes, the effect of an isw2 mutation is partially masked by a functional Sin3-Rpd3 complex. To identify the full range of genes repressed or activated by these factors and uncover hidden targets of Isw2-dependent regulation, we performed full genome expression analyses using cDNA microarrays. We find that the Isw2 complex functions mainly in repression of transcription in a parallel pathway with the Sin3-Rpd3 complex. In addition to Ume6 target genes, we find that many Ume6-independent genes are derepressed in mutants lacking functional Isw2 and Sin3-Rpd3 complexes. Conversely, we find that ume6 mutants, but not isw2 sin3 or isw2 rpd3 double mutants, have reduced fidelity of mitotic chromosome segregation, suggesting that one or more functions of Ume6p are independent of Sin3-Rpd3 and Isw2 complexes. Chromatin structure analyses of two nonmeiotic genes reveals increased DNase I sensitivity within their regulatory regions in an isw2 mutant, as seen previously for one meiotic locus. These data suggest that the Isw2 complex functions at Ume6-dependent and -independent loci to create DNase I-inaccessible chromatin structure by regulating the positioning or placement of nucleosomes.

Indexed as

Gene Expression Regulation, FungalSaccharomyces cerevisiae ProteinsAdenosine TriphosphatasesCell DivisionChromatinChromosome SegregationDeoxyribonuclease IDNA-Binding ProteinsHistone DeacetylasesMacromolecular SubstancesMutationOligonucleotide Array Sequence AnalysisPhenotypeRepressor ProteinsTranscription FactorsTranscription, GeneticAdenosine TriphosphatasesChromatinDeoxyribonuclease IDNA-Binding ProteinsHistone DeacetylasesISWI proteinMacromolecular SubstancesRepressor ProteinsSaccharomyces cerevisiae ProteinsSIN3 protein, S cerevisiaeTranscription FactorsUME6 protein, S cerevisiae

Identifiers

PMID11533234
PMCPMC99792
OpenAlexW2132236178

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.