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Open AccessJournal ArticleDOI

The fractal globule as a model of chromatin architecture in the cell

Leonid A. Mirny
- 28 Jan 2011 - 
- Vol. 19, Iss: 1, pp 37-51
TLDR
The concept of the fractal globule is presented, comparing it to other states of a polymer and focusing on its properties relevant for the biophysics of chromatin, which make it an attractive model for chromatin organization inside a cell.
Abstract
The fractal globule is a compact polymer state that emerges during polymer condensation as a result of topological constraints which prevent one region of the chain from passing across another one. This long-lived intermediate state was introduced in 1988 (Grosberg et al. 1988) and has not been observed in experiments or simulations until recently (Lieberman-Aiden et al. 2009). Recent characterization of human chromatin using a novel chromosome conformational capture technique brought the fractal globule into the spotlight as a structural model of human chromosome on the scale of up to 10 Mb (Lieberman-Aiden et al. 2009). Here, we present the concept of the fractal globule, comparing it to other states of a polymer and focusing on its properties relevant for the biophysics of chromatin. We then discuss properties of the fractal globule that make it an attractive model for chromatin organization inside a cell. Next, we connect the fractal globule to recent studies that emphasize topological constraints as a primary factor driving formation of chromosomal territories. We discuss how theoretical predictions, made on the basis of the fractal globule model, can be tested experimentally. Finally, we discuss whether fractal globule architecture can be relevant for chromatin packing in other organisms such as yeast and bacteria.

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Citations
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Journal ArticleDOI

Exploring the three-dimensional organization of genomes: interpreting chromatin interaction data

TL;DR: Several types of statistical and computational approaches that have recently been developed to analyse chromatin interaction data are described.
Journal ArticleDOI

Hi-C: a comprehensive technique to capture the conformation of genomes

TL;DR: In Hi-C, a biotin-labeled nucleotide is incorporated at the ligation junction, enabling selective purification of chimeric DNA ligation junctions followed by deep sequencing, and the compatibility of hi-C with next generation sequencing platforms makes it possible to detect chromatin interactions on an unprecedented scale.
Journal ArticleDOI

Super-resolution imaging reveals distinct chromatin folding for different epigenetic states

TL;DR: Super-resolution images reveal distinct chromatin packaging for different epigenetic states at the kilobase-to-megabase scale, a length scale that is directly relevant to genome regulation.
Journal ArticleDOI

Genome architecture: domain organization of interphase chromosomes

TL;DR: Together with microscopy and computational modeling, the results begin to yield a more coherent picture that integrates linear and three-dimensional views of chromosome organization in relation to gene regulation and other nuclear functions.
Journal ArticleDOI

Spatial Organization of the Mouse Genome and Its Role in Recurrent Chromosomal Translocations

TL;DR: A high-resolution Hi-C spatial organization map of the G1-arrested mouse pro-B cell genome is generated and high-throughput genome-wide translocation sequencing is used to map translocations from target DNA double-strand breaks (DSBs) within it.
References
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Journal ArticleDOI

Imaging intracellular fluorescent proteins at nanometer resolution.

TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
Journal ArticleDOI

Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

TL;DR: A high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores that can, in principle, reach molecular-scale resolution is developed.
Journal ArticleDOI

The landscape of somatic copy-number alteration across human cancers

Rameen Beroukhim, +86 more
- 18 Feb 2010 - 
TL;DR: It is demonstrated that cancer cells containing amplifications surrounding the MCL1 and BCL2L1 anti-apoptotic genes depend on the expression of these genes for survival, and a large majority of SCNAs identified in individual cancer types are present in several cancer types.
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