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Conserved nucleosome positioning defines replication origins

TLDR
Using high-throughput sequencing to map ORC binding and nucleosome positioning, it is shown that yeast origins are characterized by an asymmetric pattern of positioned nucleosomes flanking the ACS.
Abstract
The origin recognition complex (ORC) specifies replication origin location. The Saccharomyces cerevisiae ORC recognizes the ARS (autonomously replicating sequence) consensus sequence (ACS), but only a subset of potential genomic sites are bound, suggesting other chromosomal features influence ORC binding. Using high-throughput sequencing to map ORC binding and nucleosome positioning, we show that yeast origins are characterized by an asymmetric pattern of positioned nucleosomes flanking the ACS. The origin sequences are sufficient to maintain a nucleosome-free origin; however, ORC is required for the precise positioning of nucleosomes flanking the origin. These findings identify local nucleosomes as an important determinant for origin selection and function.

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Journal Article

The Genomic Code for Nucleosome Positioning

TL;DR: In this article, a nucleosome-DNA interaction model was proposed to predict the genome-wide organization of nucleosomes, and it was shown that genomes encode an intrinsic nucleosomal organization and that this intrinsic organization can explain ∼50% of the in-vivo positions.
Journal ArticleDOI

Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE

Sushmita Roy, +95 more
- 24 Dec 2010 - 
TL;DR: The Drosophila Encyclopedia of DNA Elements (modENCODE) project as mentioned in this paper has been used to map transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines.
Journal Article

Identification of functional elements and regulatory circuits by Drosophila modENCODE

TL;DR: Two studies identified regions of the nematode and fly genomes that show highly occupied targets (or HOT) regions where DNA was bound by more than 15 of the transcription factors analyzed and the expression of related genes were characterized.
Journal ArticleDOI

Comparative functional genomics of the fission yeasts

Nicholas Rhind, +66 more
- 20 May 2011 - 
TL;DR: Differences in gene content and regulation explain why, unlike the budding yeast of Saccharomycotina, fission yeasts cannot use ethanol as a primary carbon source and provide tools for investigation across the Schizosaccharomyces clade.
Journal ArticleDOI

Determinants and dynamics of genome accessibility

TL;DR: The interplay of nucleosome packaging and chromatin access contributes to the regulation of transcription, replication and repair in eukaryotes is discussed by reviewing the current understanding.
References
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Journal Article

The Genomic Code for Nucleosome Positioning

TL;DR: In this article, a nucleosome-DNA interaction model was proposed to predict the genome-wide organization of nucleosomes, and it was shown that genomes encode an intrinsic nucleosomal organization and that this intrinsic organization can explain ∼50% of the in-vivo positions.
Journal ArticleDOI

A genomic code for nucleosome positioning

TL;DR: This work isolated nucleosome-bound sequences at high resolution from yeast and used these sequences in a new computational approach to construct and validate experimentally a nucleosom–DNA interaction model, and to predict the genome-wide organization of nucleosomes.
Journal ArticleDOI

ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complex.

TL;DR: It is proposed that the origin recognition complex acts as the initiator protein for S. cerevisiae origins of DNA replication, and specific DNA binding by theorigin recognition complex is dependent upon the addition of ATP.
Journal ArticleDOI

Components and Dynamics of DNA Replication Complexes in S. cerevisiae: Redistribution of MCM Proteins and Cdc45p during S Phase

TL;DR: The results identify protein components of the pre-RC and a novel replication complex appearing at the G1/S transition (the RC), and suggest that after initiation MCM proteins and Cdc45p move with eukaryotic replication forks.
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