Evidence map›Paper›PMID 16966420›Full record

ArticleThe Journal of cell biology2006

The centromere-specific histone variant Cse4p (CENP-A) is essential for functional chromatin architecture at the yeast 2-microm circle partitioning locus and promotes equal plasmid segregation.

Sujata Hajra, Santanu Kumar Ghosh, Makkuni Jayaram

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Article in The Journal of cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

37 citing papers in PubMed, 55 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Sujata HajraSection of Molecular Genetics and Microbiology, University of Texas at Austin, Austin, TX 78712, USA.
Santanu Kumar Ghosh
Makkuni Jayaram
The University of Texas at Austin · US

Funding

Stable Maintenance of an Extrachromosomal Selfish DNA ElementR01GM064363 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI JAYARAM, MAKKUNI · 2002 to 2010
$2.2M
NIGMS NIH HHS GM64363NIGMS NIH HHS R01 GM064363
6 · The paper itself

Abstract

The centromere protein A homologue Cse4p is required for kinetochore assembly and faithful chromosome segregation in Saccharomyces cerevisiae. It has been regarded as the exquisite hallmark of centromeric chromatin. We demonstrate that Cse4 resides at the partitioning locus STB of the 2-microm plasmid. Cse4p-STB association is absolutely dependent on the plasmid partitioning proteins Rep1p and Rep2p and the integrity of the mitotic spindle. The kinetochore mutation ndc10-1 excludes Cse4p from centromeres without dislodging it from STB. Cse4p-STB association lasts from G1/S through late telophase during the cell cycle. The release of Cse4p from STB chromatin is likely mediated through spindle disassembly. A lack of functional Cse4p disrupts the remodeling of STB chromatin by the RSC2 complex, negates Rep2p binding and cohesin assembly at STB, and causes plasmid missegregation. Poaching of a specific histone variant by the plasmid to mark its partitioning locus with a centromere tag reveals yet another one of the molecular trickeries it performs for achieving chromosome- like fidelity in segregation.

Indexed as

Cell Cycle ProteinsCell DivisionCentromereChromatinChromosomal Proteins, Non-HistoneChromosome SegregationCohesinsDNA-Binding ProteinsGenes, cdcKinetochoresMutationNuclear ProteinsPlasmidsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpindle ApparatusCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsCSE4 protein, S cerevisiaeDNA-Binding ProteinsNuclear ProteinsREP1 protein, S cerevisiaeREP2 protein, S cerevisiaeRSC2 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsTrans-Activators

Identifiers

PMID16966420
PMCPMC2064333
OpenAlexW2129099821

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.