Insights into Interphase Large-Scale Chromatin Structure from Analysis of Engineered Chromosome Regions

被引:18
作者
Belmont, A. S. [1 ]
Hu, Y.
Sinclair, P. B.
Wu, W.
Bian, Q.
Kireev, I.
机构
[1] Univ Illinois, Dept Cell & Dev Biol, Urbana, IL 61801 USA
来源
NUCLEAR ORGANIZATION AND FUNCTION | 2010年 / 75卷
基金
美国国家卫生研究院;
关键词
IN-VIVO; NUCLEAR ARCHITECTURE; SC-35; DOMAINS; DNA; ORGANIZATION; GENES; VISUALIZATION; TRANSCRIPTION; LOCALIZATION; CONDENSATION;
D O I
10.1101/sqb.2010.75.050
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 chromatin folds into mitotic and interphase chromosomes has remained a difficult question for many years. We have used three generations of engineered chromosome regions as a means of visualizing specific chromosome regions in live cells and cells fixed under conditions that preserve large-scale chromatin structure. Our results confirm the existence of large-scale chromatin domains and fibers formed by the folding of 10-nm and 30-nm chromatin fibers into larger, spatially distinct domains. Transcription at levels within severalfold of the levels measured for endogenous loci occur within these large-scale chromatin structures on a condensed template linearly compacted several hundred fold to 1000-fold relative to B-form DNA. However, transcriptional induction is accompanied by a severalfold decondensation of this large-scale chromatin structure that propagates hundreds of kilobases beyond the induced gene. Examination of engineered chromosome regions in mouse embryonic stem cells (ESCs) and differentiated cells suggests a surprising degree of plasticity in this large-scale chromatin structure, allowing long-range DNA interactions within the context of large-scale chromatin fibers. Recapitulation of gene-specific differences in large-scale chromatin conformation and nuclear positioning using these engineered chromosome regions will facilitate identification of cis and trans determinants of interphase chromosome architecture.
引用
收藏
页码:453 / 460
页数:8
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