De novo kinetochore assembly requires the centromeric histone H3 variant. - Wikidata - wikimedia - TriplyDB

De novo kinetochore assembly requires the centromeric histone H3 variant.

De novo kinetochore assembly requires the centromeric histone H3 variant.

http://www.wikidata.org/entity/Q28941168

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Re-replication of a centromere induces chromosomal instability and aneuploidy Roles for the conserved spc105p/kre28p complex in kinetochore-microtubule binding and the spindle assembly checkpoint.SWI/SNF-like chromatin remodeling factor Fun30 supports point centromere function in S. cerevisiae.Gcn5p plays an important role in centromere kinetochore function in budding yeast.Histone H3 localizes to the centromeric DNA in budding yeast The unconventional kinetoplastid kinetochore: from discovery toward functional understanding DNA binding of centromere protein C (CENPC) is stabilized by single-stranded RNA A coordinated interdependent protein circuitry stabilizes the kinetochore ensemble to protect CENP-A in the human pathogenic yeast Candida albicans CaMtw1, a member of the evolutionarily conserved Mis12 kinetochore protein family, is required for efficient inner kinetochore assembly in the pathogenic yeast Candida albicans.Control of the spindle checkpoint by lateral kinetochore attachment and limited Mad1 recruitment.Plasticity of fission yeast CENP-A chromatin driven by relative levels of histone H3 and H4.Efficient yeast ChIP-Seq using multiplex short-read DNA sequencing.A strategy for constructing aneuploid yeast strains by transient nondisjunction of a target chromosome The kinetochore Towards building a chromosome segregation machine.The life and miracles of kinetochores.Live-cell analysis of kinetochore-microtubule interaction in budding yeast.The CNA1 histone of the ciliate Tetrahymena thermophila is essential for chromosome segregation in the germline micronucleus Epigenetic specification of centromeres.Kinetochore function and chromosome segregation rely on critical residues in histones H3 and H4 in budding yeast.Endogenous transcription at the centromere facilitates centromere activity in budding yeast.The overexpression of a Saccharomyces cerevisiae centromeric histone H3 variant mutant protein leads to a defect in kinetochore biorientation CENP-A exceeds microtubule attachment sites in centromere clusters of both budding and fission yeast.Synergistic Control of Kinetochore Protein Levels by Psh1 and Ubr2.Regulation of Budding Yeast CENP-A levels Prevents Misincorporation at Promoter Nucleosomes and Transcriptional Defects.Synthetic physical interactions map kinetochore regulators and regions sensitive to constitutive Cdc14 localization.A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere.Pericentric chromatin is organized into an intramolecular loop in mitosis.The composition, functions, and regulation of the budding yeast kinetochore Sir protein-independent repair of dicentric chromosomes in Saccharomyces cerevisiae.The interplay between chromosome stability and cell cycle control explored through gene-gene interaction and computational simulation Pericentromeric sister chromatid cohesion promotes kinetochore biorientation.Hierarchical inactivation of a synthetic human kinetochore by a chromatin modifier.The process of kinetochore assembly in yeasts.Synthetic Physical Interactions Map Kinetochore-Checkpoint Activation Regions.Condensin function at centromere chromatin facilitates proper kinetochore tension and ensures correct mitotic segregation of sister chromatids.The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4.The requirement for the Dam1 complex is dependent upon the number of kinetochore proteins and microtubules Molecular basis of CENP-C association with the CENP-A nucleosome at yeast centromeres.The 19S proteasome subunit Rpt3 regulates distribution of CENP-A by associating with centromeric chromatin.

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De novo kinetochore assembly requires the centromeric histone H3 variant.

http://www.wikidata.org/entity/Q28941168

description

2005 nî lūn-bûn

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2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

De novo kinetochore assembly requires the centromeric histone H3 variant.

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De novo kinetochore assembly requires the centromeric histone H3 variant.

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type

label

De novo kinetochore assembly requires the centromeric histone H3 variant.

@ast

De novo kinetochore assembly requires the centromeric histone H3 variant.

@en

prefLabel

De novo kinetochore assembly requires the centromeric histone H3 variant.

@ast

De novo kinetochore assembly requires the centromeric histone H3 variant.

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MBC.E05-08-0771

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Molecular Biology of the Cell

P1476

De novo kinetochore assembly requires the centromeric histone H3 variant

@en

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Andrea R Castillo

http://www.w3.org/2001/XMLSchema#string

Kimberly A Collins

http://www.w3.org/2001/XMLSchema#string

Sean Y Tatsutani

http://www.w3.org/2001/XMLSchema#string

P2860

Specification of kinetochore-forming chromatin by the histone H3 variant CENP-A

Human centromere chromatin protein hMis12, essential for equal segregation, is independent of CENP-A loading pathway

A delay in the Saccharomyces cerevisiae cell cycle that is induced by a dicentric chromosome and dependent upon mitotic checkpoints

CENP-A is phosphorylated by Aurora B kinase and plays an unexpected role in completion of cytokinesis

NDC10: a gene involved in chromosome segregation in Saccharomyces cerevisiae

Functional analysis of kinetochore assembly in Caenorhabditis elegans.

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

Uninterrupted MCM2-7 function required for DNA replication fork progression.

Differential kinetochore protein requirements for establishment versus propagation of centromere activity in Saccharomyces cerevisiae.

Molecular analysis of kinetochore-microtubule attachment in budding yeast.

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5649-5660

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10.1091/MBC.E05-08-0771

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12

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16207811

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