Topology, structures, and energy landscapes of human chromosomes
Bin Zhang,Peter G. Wolynes +1 more
TL;DR: An energy landscape model of the chromosome is presented that reproduces a diverse set of experimental measurements and enables quantitative predictions of chromosome structure and topology and provides mechanistic insight into the role of 3D genome organization in gene regulation and cell differentiation.
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Abstract: Chromosome conformation capture experiments provide a rich set of data concerning the spatial organization of the genome. We use these data along with a maximum entropy approach to derive a least-biased effective energy landscape for the chromosome. Simulations of the ensemble of chromosome conformations based on the resulting information theoretic landscape not only accurately reproduce experimental contact probabilities, but also provide a picture of chromosome dynamics and topology. The topology of the simulated chromosomes is probed by computing the distribution of their knot invariants. The simulated chromosome structures are largely free of knots. Topologically associating domains are shown to be crucial for establishing these knotless structures. The simulated chromosome conformations exhibit a tendency to form fibril-like structures like those observed via light microscopy. The topologically associating domains of the interphase chromosome exhibit multistability with varying liquid crystalline ordering that may allow discrete unfolding events and the landscape is locally funneled toward “ideal” chromosome structures that represent hierarchical fibrils of fibrils.
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Funnels, Pathways and the Energy Landscape of Protein Folding: A Synthesis
TL;DR: In this paper, the authors use the energy landscape approach to understand the structure of protein foldings and the mechanism of protein folding, and the success of energy landscape ideas in protein structure prediction.
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Quentin Szabo,Daniel Jost,Jia-Ming Chang,Diego I. Cattoni,Giorgio L. Papadopoulos,Boyan B. Bonev,Tom Sexton,Julian Gurgo,Caroline Jacquier,Marcelo Nollmann,Frédéric Bantignies,Giacomo Cavalli +11 more
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De novo prediction of human chromosome structures: Epigenetic marking patterns encode genome architecture.
Michele Di Pierro,Ryan R. Cheng,Erez Lieberman Aiden,Erez Lieberman Aiden,Peter G. Wolynes,José N. Onuchic +5 more
TL;DR: It is demonstrated that it is possible to predict how a genome will fold based on the epigenetic marks that decorate chromatin, and that de novo structure prediction for whole genomes may be increasingly possible.
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References
Comprehensive mapping of long-range interactions reveals folding principles of the human genome.
Erez Lieberman Aiden,Nynke L. van Berkum,Louise Williams,Maxim Imakaev,Tobias Ragoczy,Tobias Ragoczy,Agnes Telling,Agnes Telling,Ido Amit,Bryan R. Lajoie,Peter J. Sabo,Michael O. Dorschner,Richard Sandstrom,Bradley E. Bernstein,Bradley E. Bernstein,Michaël Bender,Mark Groudine,Mark Groudine,Andreas Gnirke,John A. Stamatoyannopoulos,Leonid A. Mirny,Eric S. Lander,Eric S. Lander,Job Dekker +23 more
TL;DR: Hi-C is described, a method that probes the three-dimensional architecture of whole genomes by coupling proximity-based ligation with massively parallel sequencing and demonstrates the power of Hi-C to map the dynamic conformations of entire genomes.
Topological domains in mammalian genomes identified by analysis of chromatin interactions
Jesse R. Dixon,Siddarth Selvaraj,Siddarth Selvaraj,Feng Yue,Audrey Kim,Yan-Yan Li,Yin-Zhong Shen,Ming Hu,Jun Liu,Bing Ren,Bing Ren +10 more
TL;DR: It is found that the boundaries of topological domains are enriched for the insulator binding protein CTCF, housekeeping genes, transfer RNAs and short interspersed element (SINE) retrotransposons, indicating that these factors may have a role in establishing the topological domain structure of the genome.
The energy landscapes and motions of proteins.
TL;DR: The concepts that emerge from studies of the conformational substates and the motions between them permit a quantitative discussion of one simple reaction, the binding of small ligands such as carbon monoxide to myoglobin.
3.2K
DNA topoisomerases: structure, function, and mechanism.
TL;DR: Surprisingly, despite little or no sequence homology, both type IA and type IIA topoisomerases from prokaryotes and the typeIIA enzymes from eukaryotes share structural folds that appear to reflect functional motifs within critical regions of the enzymes.
2.7K
Funnels, pathways, and the energy landscape of protein folding: A synthesis
TL;DR: The work unifies several previously proposed ideas concerning the mechanism protein folding and delimits the regions of validity of these ideas under different thermodynamic conditions.
2.4K
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