Evidence map›Paper›PMID 17548816›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Scm3, an essential Saccharomyces cerevisiae centromere protein required for G2/M progression and Cse4 localization.

Sam Stoler, Kelly Rogers, Scott Weitze, Lisa Morey, Molly Fitzgerald-Hayes, Richard E Baker

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
27.1field-weighted citation impact, top 1% 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

127 citing papers in PubMed, 187 citations in OpenAlex.

  1. Structure and function of the centromere and inner kinetochore.Nature reviews. Molecular cell biology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. A brief historical perspective on cell cycle control of CENP-A assembly and inheritance.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Histone variants and chromatin structure, update of advances.Computational and structural biotechnology journal · 2023
    Review
  18. Article
  19. Kinetochore assembly throughout the cell cycle.Seminars in cell & developmental biology · 2021
    Article
  20. Review

67 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

6 authors at 2 institutions in 1 country.

Sam StolerDepartment of Biochemistry and Molecular Biology, University of Massachusetts, Amherst, MA 01003, USA.
Kelly Rogers
Scott Weitze
Lisa Morey
Molly Fitzgerald-Hayes
Richard E Baker
University of Massachusetts Amherst · USUniversity of Massachusetts Chan Medical School · US

Funding

Training Program in Cancer TherapeuticsT32CA117846 · NCI · UNIVERSITY OF CINCINNATI · PI PRICE, CAROLYN M, TAKIAR, VINITA · 2006 to 2022
$6.5M
Assembling a Centric NucleosomeR01GM061120 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BAKER, RICHARD E · 2001 to 2004
$1.1M
FUNCTIONAL ANALYSIS OF CENTROMERIC CHROMATIN IN YEASTR01GM054766 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI FITZGERALD-HAYES, MOLLY · 1996 to 2003
$1.1M
NCI NIH HHS T32 CA117846NIGMS NIH HHS GM54766NIGMS NIH HHS GM61120NIGMS NIH HHS R01 GM054766NIGMS NIH HHS R01 GM061120
6 · The paper itself

Abstract

A universal mark of centromeric chromatin is its packaging by a variant of histone H3 known as centromeric H3 (CenH3). The mechanism by which CenH3s are incorporated specifically into centromere DNA or the specialized function they serve there is not known. In a genetic approach to identify factors involved in CenH3 deposition, we screened for dosage suppressors of a temperature-sensitive cse4 allele in Saccharomyces cerevisiae (Cse4 is the S. cerevisiae CenH3). Independent screens yielded ORF YDL139C, which we named SCM3. Dosage suppression by SCM3 was specific for alleles affecting the histone fold domain of Cse4. Copurification and two-hybrid studies showed that Scm3 and Cse4 interact in vivo, and chromatin immunoprecipitation revealed that Scm3, like Cse4, is found associated with centromere DNA. Scm3 contains two essential protein domains, a Leu-rich nuclear export signal and a heptad repeat domain that is widely conserved in fungi. A conditional scm3 allele was generated to allow us to deplete Scm3. Upon Scm3 depletion, cells undergo a Mad2-dependent G2/M arrest, and centromere localization of Cse4 is perturbed. We suggest that S. cerevisiae Scm3 defines a previously undescribed family of fungal kinetochore proteins important for CenH3 localization.

Indexed as

G2 PhaseMitosisAllelesAmino Acid MotifsAmino Acid SequenceAmino Acid SubstitutionBayes TheoremCentromereChromatin ImmunoprecipitationChromosomal Proteins, Non-HistoneDNA-Binding ProteinsGenetic Complementation TestHemagglutininsLeucineModels, GeneticMolecular Sequence DataChromosomal Proteins, Non-HistoneCSE4 protein, S cerevisiaeDNA-Binding ProteinsHemagglutininsLeucineNuclear Export SignalsSaccharomyces cerevisiae ProteinsScm3 protein, S cerevisiaeThreonine

Identifiers

PMID17548816
PMCPMC1885823
OpenAlexW1995275121

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.