Genome information processing by the INO80 chromatin remodeler positions nucleosomes

Autor: Kevin Schall, Vanessa Niebauer, Manuela Moldt, Nils Krietenstein, Elisa Oberbeckmann, Sebastian Eustermann, Karl-Peter Hopfner, Tobias Straub, Yingfei Wang, Philipp Korber, Remo Rohs
Rok vydání: 2020
Předmět:
0301 basic medicine
Saccharomyces cerevisiae Proteins
Science
General Physics and Astronomy
Chromatin remodelling
Saccharomyces cerevisiae
Computational biology
Biology
Genome
General Biochemistry
Genetics and Molecular Biology

Article
DNA sequencing
Histones
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Allosteric Regulation
Animals
Drosophila Proteins
Humans
Nucleosome
DNA
Fungal

Promoter Regions
Genetic

030304 developmental biology
0303 health sciences
Multidisciplinary
Fungal genetics
General Chemistry
Chromatin Assembly and Disassembly
Linker DNA
Recombinant Proteins
Nucleosomes
Chromatin
030104 developmental biology
Drosophila melanogaster
Histone
Gene Expression Regulation
chemistry
Larva
Enzyme mechanisms
biology.protein
Nucleic Acid Conformation
Genome
Fungal

Sequence motif
030217 neurology & neurosurgery
DNA
Zdroj: Nature Communications, Vol 12, Iss 1, Pp 1-19 (2021)
bioRxiv
Nature Communications
Popis: The fundamental molecular determinants by which ATP-dependent chromatin remodelers organize nucleosomes across eukaryotic genomes remain largely elusive. Here, chromatin reconstitutions on physiological, whole-genome templates reveal how remodelers read and translate genomic information into nucleosome positions. Using the yeast genome and the multi-subunit INO80 remodeler as a paradigm, we identify DNA shape/mechanics encoded signature motifs as sufficient for nucleosome positioning and distinct from known DNA sequence preferences of histones. INO80 processes such information through an allosteric interplay between its core- and Arp8-modules that probes mechanical properties of nucleosomal and linker DNA. At promoters, INO80 integrates this readout of DNA shape/mechanics with a readout of co-evolved sequence motifs via interaction with general regulatory factors bound to these motifs. Our findings establish a molecular mechanism for robust and yet adjustable +1 nucleosome positioning and, more generally, remodelers as information processing hubs that enable active organization and allosteric regulation of the first level of chromatin.
DNA sequence preferences or statistical positioning of histones has not explained genomic patterns of nucleosome organisation in vivo. Here, the authors establish DNA shape/mechanics as key elements that have evolved together with binding sites of DNA sequence-specific barriers so that such information directs nucleosome positioning by chromatin remodelers.
Databáze: OpenAIRE