scholarly journals Spatial genome organization in the formation of chromosomal translocations

2007 ◽  
Vol 17 (1) ◽  
pp. 80-90 ◽  
Author(s):  
Karen J. Meaburn ◽  
Tom Misteli ◽  
Evi Soutoglou
Keyword(s):  
Genome Organization ◽  
Chromosomal Translocations ◽  
Spatial Genome Organization

scholarly journals Comparative analysis of 2D and 3D distance measurements to study spatial genome organization

Methods ◽  
2017 ◽  
Vol 123 ◽  
pp. 47-55 ◽  
Author(s):  
Elizabeth H. Finn ◽  
Gianluca Pegoraro ◽  
Sigal Shachar ◽  
Tom Misteli
Keyword(s):  
Comparative Analysis ◽  
Genome Organization ◽  
Distance Measurements ◽  
Spatial Genome Organization ◽  
2D And 3D

scholarly journals Understanding Spatial Genome Organization: Methods and Insights

2016 ◽  
Vol 14 (1) ◽  
pp. 7-20 ◽  
Author(s):  
Vijay Ramani ◽  
Jay Shendure ◽  
Zhijun Duan
Keyword(s):  
Genome Organization ◽  
Spatial Genome Organization

scholarly journals Technologies to study spatial genome organization: beyond 3C

2019 ◽  
Author(s):  
Nadine Übelmesser ◽  
Argyris Papantonis
Keyword(s):  
Genome Organization ◽  
Nuclear Organization ◽  
Three Dimensional ◽  
Nuclear Space ◽  
Chromosome Conformation ◽  
Novel Variants ◽  
Cell Processes ◽  
Systematic Biases ◽  
And Function ◽  
Spatial Genome Organization

Abstract The way that chromatin is organized in three-dimensional nuclear space is now acknowledged as a factor critical for the major cell processes, like transcription, replication and cell division. Researchers have been armed with new molecular and imaging technologies to study this structure-to-function link of genomes, spearheaded by the introduction of the ‘chromosome conformation capture’ technology more than a decade ago. However, this technology is not without shortcomings, and novel variants and orthogonal approaches are being developed to overcome these. As a result, the field of nuclear organization is constantly fueled by methods of increasing resolution and/or throughput that strive to eliminate systematic biases and increase precision. In this review, we attempt to highlight the most recent advances in technology that promise to provide novel insights on how chromosomes fold and function.

scholarly journals An integrated 3-Dimensional Genome Modeling Engine for data-driven simulation of spatial genome organization

2016 ◽  
Vol 26 (12) ◽  
pp. 1697-1709 ◽  
Author(s):  
Przemysław Szałaj ◽  
Zhonghui Tang ◽  
Paul Michalski ◽  
Michal J. Pietal ◽  
Oscar J. Luo ◽  
...  
Keyword(s):  
Genome Organization ◽  
Data Driven ◽  
3 Dimensional ◽  
Spatial Genome Organization

Mapping and Visualizing Spatial Genome Organization

2016 ◽  
pp. 359-383
Author(s):  
Christopher J. F. Cameron ◽  
James Fraser ◽  
Mathieu Blanchette ◽  
Josée Dostie
Keyword(s):  
Genome Organization ◽  
Spatial Genome Organization

scholarly journals Spatial Genome Organization: From Development to Disease

2019 ◽  
Vol 7 ◽  
Author(s):  
Aishwarya Sivakumar ◽  
Jose I. de las Heras ◽  
Eric C. Schirmer
Keyword(s):  
Genome Organization ◽  
Spatial Genome Organization

scholarly journals Comparative analysis of 2D and 3D distance measurements to study spatial genome organization

2016 ◽  
Author(s):  
Elizabeth H. Finn ◽  
Gianluca Pegoraro ◽  
Sigal Shachar ◽  
Tom Misteli
Keyword(s):  
Genome Organization ◽  
Spatial Organization ◽  
Theoretical Models ◽  
3D Analysis ◽  
Distance Measurements ◽  
Accuracy And Precision ◽  
Distance Distributions ◽  
Cell Type Specific ◽  
Spatial Genome Organization ◽  
2D And 3D

ABSTRACTThe spatial organization of eukaryotic genomes is non-random, cell-type specific, and has been linked to cellular function. The investigation of spatial organization has traditionally relied extensively on fluorescence microscopy. The validity of the imaging methods used to probe spatial genome organization often depends on the accuracy and precision of distance measurements. Imaging-based measurements may either use 2 dimensional datasets or 3D datasets including the z-axis information in image stacks. Here we compare the suitability of 2D versus 3D distance measurements in the analysis of various features of spatial genome organization. We find in general good agreement between 2D and 3D analysis with higher convergence of measurements as the interrogated distance increases, especially in flat cells. Overall, 3D distance measurements are more accurate than 2D distances, but are also more prone to noise. In particular, z-stacks are prone to error due to imaging properties such as limited resolution along the z-axis and optical aberrations, and we also find significant deviations from unimodal distance distributions caused by low sampling frequency in z. These deviations can be ameliorated by sampling at much higher frequency in the z-direction. We conclude that 2D distances are preferred for comparative analyses between cells, but 3D distances are preferred when comparing to theoretical models in large samples of cells. In general, 2D distance measurements remain preferable for many applications of analysis of spatial genome organization.

scholarly journals Heterogeneity and Intrinsic Variation in Spatial Genome Organization

2017 ◽  
Author(s):  
Elizabeth H. Finn ◽  
Gianluca Pegoraro ◽  
Hugo B. Brandão ◽  
Anne-Laure Valton ◽  
Marlies E. Oomen ◽  
...  
Keyword(s):  
Genome Organization ◽  
Single Cells ◽  
Human Fibroblasts ◽  
Intrinsic Variability ◽  
Cell Level ◽  
3D Genome ◽  
3D Space ◽  
A Cell ◽  
Spatial Genome Organization ◽  
Independent Behavior

AbstractThe genome is hierarchically organized in 3D space and its architecture is altered in differentiation, development and disease. Some of the general principles that determine global 3D genome organization have been established. However, the extent and nature of cell-to-cell and cell-intrinsic variability in genome architecture are poorly characterized. Here, we systematically probe the heterogeneity in genome organization in human fibroblasts by combining high-resolution Hi-C datasets and high-throughput genome imaging. Optical mapping of several hundred genome interaction pairs at the single cell level demonstrates low steady-state frequencies of colocalization in the population and independent behavior of individual alleles in single nuclei. Association frequencies are determined by genomic distance, higher-order chromatin architecture and chromatin environment. These observations reveal extensive variability and heterogeneity in genome organization at the level of single cells and alleles and they demonstrate the coexistence of a broad spectrum of chromatin and genome conformations in a cell population.

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