Evidence map›Paper›PMID 12417720›Full record

ArticleMolecular and cellular biology2002

HTL1 encodes a novel factor that interacts with the RSC chromatin remodeling complex in Saccharomyces cerevisiae.

Martin J Romeo, Melinda L Angus-Hill, Andrew K Sobering, Yoshiaki Kamada, Bradley R Cairns, David E Levin

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
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  11. Cell wall integrity signaling in Saccharomyces cerevisiae.Microbiology and molecular biology reviews : MMBR · 2005
    Review
  12. A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  13. Article
  14. 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

6 authors at 3 institutions in 1 country.

Martin J RomeoDepartment of Biochemistry & Molecular Biology, Bloomberg School of Public Health, The Johns Hopkins University, Baltimore, Maryland 21205, USA.
Melinda L Angus-Hill
Andrew K Sobering
Yoshiaki Kamada
Bradley R Cairns
David E Levin
Johns Hopkins University · USHoward Hughes Medical Institute · USUniversity of Utah · US

Funding

TRAINING IN AREAS FUNDAMENTAL TO CANCER RESEARCHT32CA009110 · NCI · JOHNS HOPKINS UNIVERSITY · PI MATUNIS, MICHAEL J., WEERARATNA, ASHANI T · 1985 to 2025
$13.1M
ROLE OF PROTEIN KINASE C IN YEAST GROWTH CONTROLR01GM048533 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LEVIN, DAVID E. · 1992 to 2025
$7.8M
TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
ANALYSIS OF THE CHROMATIN-REMODELING COMPLEX RSCR01GM060415 · NIGMS · UNIVERSITY OF UTAH · PI CAIRNS, BRADLEY R. · 1999 to 2011
$3.1M
RIN1, A NOVEL RAS-INHIBITORY PROTEIN IN YEASTR01GM067698 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI LEVIN, DAVID E. · 2003 to 2006
$1.0M
NCI NIH HHS 5T32CA09110NCI NIH HHS T32 CA009110NIGMS NIH HHS GM48533NIGMS NIH HHS GM60415NIGMS NIH HHS R01 GM048533NIGMS NIH HHS R01 GM060415NIGMS NIH HHS R01 GM067698NIGMS NIH HHS T32 GM007464NIGMS NIH HHS T32GM07464
6 · The paper itself

Abstract

RSC is an essential chromatin remodeling complex in Saccharomyces cerevisiae that performs central roles in transcriptional regulation and cell cycle progression. Here we identify Htl1 as a novel factor that associates with the RSC complex both physically and functionally. We isolated HTL1 through a genetic screen for mutants that displayed additive growth defects with a conditional mutation in the protein kinase C gene (PKC1), which has been suggested through genetic connections to interact functionally with RSC. Several lines of evidence connect HTL1 to RSC function. First, an htl1Delta mutant displayed temperature-sensitive growth and a G(2)/M cell cycle arrest at restrictive temperatures, a phenotype similar to that of strains with conditional mutations in essential RSC components. Second, we isolated RSC3, which encodes a component of the RSC complex, as a dosage suppressor of the htl1Delta growth arrest. Third, an htl1Delta mutant displayed additive growth defects with conditional rsc3 alleles. Fourth, overexpression of HTL1 suppressed the growth defect of a strain with a conditional mutation in another RSC component, RSC8. Finally, we demonstrate that Htl1 is a nuclear protein that can associate in vivo with a fraction of the RSC complex. We propose that an RSC-Htl1 complex acts coordinately with protein kinase C to regulate the G(2)/M transition.

Indexed as

Cell CycleCell Cycle ProteinsCell DivisionCell WallChromatinDNA-Binding ProteinsFlow CytometryGene Expression Regulation, FungalGenes, FungalMacromolecular SubstancesMutationNuclear ProteinsProtein Kinase CSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSuppression, GeneticCell Cycle ProteinsChromatinDNA-Binding ProteinsHTL1 protein, S cerevisiaeMacromolecular SubstancesNuclear ProteinsProtein Kinase CRSC complex, S cerevisiaeSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID12417720
PMCPMC134067
OpenAlexW2099361940

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.