Chromosome dynamics and folding in eukaryotes: Insights from live cell microscopy

被引:23
作者
Bystricky, Kerstin [1 ,2 ]
机构
[1] Univ Toulouse, UPS, Toulouse, France
[2] CNRS, LBME, Lab Biol Mol Eucaryote, F-32062 Toulouse, France
关键词
Live cell fluroescence microscopy; Chromosome conformation; Transcription; INTERPHASE CHROMOSOMES; NUCLEAR-ORGANIZATION; CHROMATIN FIBER; GENE-EXPRESSION; GENOMIC LOCI; YEAST; SINGLE; REVEALS; ARCHITECTURE; CONFORMATION;
D O I
10.1016/j.febslet.2015.07.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
How chromosomes are folded and how this folding relates to function remain fundamental questions. Answering them is rendered difficult by the stochasticity of chromatin fiber motion which inevitably results in heterogeneity of the populations analyzed. Even if single cell analyses are beginning to yield precious insights, how can we determine whether a snapshot of position is related to function of the probed locus or cell-type? Fluorescence labeling of DNA at single or multiple loci allows determination of their position relative to nuclear landmarks and to each other, enabling us to derive physical parameters of the underlying chromatin fiber. Here I review the contribution of quantitative spatial and temporal analysis of labeled DNA to our understanding of chromosome conformation in different cell types, highlighting live cell imaging techniques and large scale geometrical analysis of multiple loci in 3D. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3014 / 3022
页数:9
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