scispace - formally typeset
Open AccessJournal ArticleDOI

Tripartite organization of centromeric chromatin in budding yeast

TLDR
The authors' detection of two forms of CenH3 nucleosomes in the yeast genome, a singly wrapped particle at the functional centromere and octamer-sized particles on chromosome arms, reconcile seemingly conflicting in vivo and in vitro observations.
Abstract
The centromere is the genetic locus that organizes the proteinaceous kinetochore and is responsible for attachment of the chromosome to the spindle at mitosis and meiosis. In most eukaryotes, the centromere consists of highly repetitive DNA sequences that are occupied by nucleosomes containing the CenH3 histone variant, whereas in budding yeast, a ∼120-bp centromere DNA element (CDE) that is sufficient for centromere function is occupied by a single right-handed histone variant CenH3 (Cse4) nucleosome. However, these in vivo observations are inconsistent with in vitro evidence for left-handed octameric CenH3 nucleosomes. To help resolve these inconsistencies, we characterized yeast centromeric chromatin at single base-pair resolution. Intact particles containing both Cse4 and H2A are precisely protected from micrococcal nuclease over the entire CDE of all 16 yeast centromeres in both solubilized chromatin and the insoluble kinetochore. Small DNA-binding proteins protect CDEI and CDEIII and delimit the centromeric nucleosome to the ∼80-bp CDEII, only enough for a single DNA wrap. As expected for a tripartite organization of centromeric chromatin, loss of Cbf1 protein, which binds to CDEI, both reduces the size of the centromere-protected region and shifts its location toward CDEIII. Surprisingly, Cse4 overproduction caused genome-wide misincorporation of nonfunctional CenH3-containing nucleosomes that protect ∼135 base pairs and are preferentially enriched at sites of high nucleosome turnover. Our detection of two forms of CenH3 nucleosomes in the yeast genome, a singly wrapped particle at the functional centromere and octamer-sized particles on chromosome arms, reconcile seemingly conflicting in vivo and in vitro observations.

read more

Citations
More filters
Journal ArticleDOI

An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites

TL;DR: Skene and Henikoff as discussed by the authors developed a new method, called CUTR, which means that protein-DNA interactions are more likely to be maintained in their natural state, which can be used to more accurately identify where transcription factors bind to DNA from yeast and human cells.
Journal ArticleDOI

A Molecular View of Kinetochore Assembly and Function.

TL;DR: A broad summary of progress in the elucidation of the composition of the kinetochore and the identification of various physical and functional modules within its substructure has led to a much deeper molecular understanding of kinetchore organization and the origins of its functional output.
Journal ArticleDOI

Understanding nucleosome dynamics and their links to gene expression and DNA replication.

TL;DR: Nucleosome dynamics are governed by a complex interplay of histone composition, histone post-translational modifications, nucleosome occupancy and positioning within chromatin, which are influenced by numerous regulatory factors, including general Regulatory factors, chromatin remodellers, chaperones and polymerases.
Journal ArticleDOI

A two-step mechanism for epigenetic specification of centromere identity and function

TL;DR: Using gene targeting in human cells and fission yeast, chromatin containing the centromere-specific histone H3 variant CENP-A is demonstrated to be the epigenetic mark that acts through a two-step mechanism to identify, maintain and propagateCentromere function indefinitely.
Journal ArticleDOI

Subnucleosomal Structures and Nucleosome Asymmetry across a Genome

TL;DR: This work uses chromatin immunoprecipitation-exonuclease (ChIP-exo) to resolve the organization of individual histones on a genomic scale and detects widespread subnucleosomal structures in dynamic chromatin, including what appear to be half-n nucleosomes consisting of one copy of each histone.
References
More filters
Journal ArticleDOI

An improved map of conserved regulatory sites for Saccharomyces cerevisiae

TL;DR: In this paper, two complementary computational strategies for conservation-based motif discovery improves the ability to identify the specificity of transcriptional regulators from genome-wide chromatin immunoprecipitation data.

An improved map of conserved regulatory sites for Saccharomyces cerevisiae

TL;DR: Improved versions of two conservation-based motif discovery algorithms, PhyloCon and Converge, are reported, which improve the ability to identify the specificity of transcriptional regulators from genome-wide chromatin immunoprecipitation data.
Journal ArticleDOI

Dynamics of Replication-Independent Histone Turnover in Budding Yeast

TL;DR: It is found that nucleosomes at promoters are replaced more rapidly than at coding regions and that replacement rates over coding regions correlate with polymerase density, which suggests that rapid histone turnover serves to functionally separate chromatin domains and prevent spread of histone states.
Journal ArticleDOI

Stepwise histone replacement by SWR1 requires dual activation with histone H2A.Z and canonical nucleosome.

TL;DR: It is shown that promoter-proximal nucleosomes are highly heterogeneous for H2A.Z in Saccharomyces cerevisiae, with substantial representation of nucleosome containing one, two, or zero H2a.Z molecules.
Journal ArticleDOI

Cse4p Is a Component of the Core Centromere of Saccharomyces cerevisiae

TL;DR: Direct evidence is presented that Cse4p, a histone H3 variant, is a structural component of the core centromere of S. cerevisiae, and results suggest the kinetochore is assembled on a specialized centromeric nucleosome containing CSE4p.
Related Papers (5)