Author
Listed:
- Elisa Oberbeckmann
(Ludwig-Maximilians-Universität München
Max Planck Institute for Biophysical Chemistry)
- Nils Krietenstein
(Ludwig-Maximilians-Universität München
University of Massachusetts Medical School)
- Vanessa Niebauer
(Ludwig-Maximilians-Universität München
Ludwig-Maximilians-Universität München)
- Yingfei Wang
(University of Southern California)
- Kevin Schall
(Ludwig-Maximilians-Universität München
Ludwig-Maximilians-Universität München)
- Manuela Moldt
(Ludwig-Maximilians-Universität München
Ludwig-Maximilians-Universität München)
- Tobias Straub
(Ludwig-Maximilians-Universität München)
- Remo Rohs
(University of Southern California)
- Karl-Peter Hopfner
(Ludwig-Maximilians-Universität München
Ludwig-Maximilians-Universität München)
- Philipp Korber
(Ludwig-Maximilians-Universität München)
- Sebastian Eustermann
(Ludwig-Maximilians-Universität München
Ludwig-Maximilians-Universität München
Structural and Computational Biology Unit)
Abstract
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.
Suggested Citation
Elisa Oberbeckmann & Nils Krietenstein & Vanessa Niebauer & Yingfei Wang & Kevin Schall & Manuela Moldt & Tobias Straub & Remo Rohs & Karl-Peter Hopfner & Philipp Korber & Sebastian Eustermann, 2021.
"Genome information processing by the INO80 chromatin remodeler positions nucleosomes,"
Nature Communications, Nature, vol. 12(1), pages 1-19, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23016-z
DOI: 10.1038/s41467-021-23016-z
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