An Overview of Genome Organization and How We Got There: from FISH to Hi-C

被引:146
作者
Fraser, James [1 ,2 ]
Williamson, Iain [3 ]
Bickmore, Wendy A. [3 ]
Dostie, Josee [1 ,2 ]
机构
[1] McGill Univ, Dept Biochem, Montreal, PQ, Canada
[2] McGill Univ, Goodman Canc Res Ctr, Montreal, PQ, Canada
[3] Univ Edinburgh, MRC Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会; 加拿大健康研究院;
关键词
CHROMOSOME CONFORMATION CAPTURE; BETA-GLOBIN LOCUS; ORDER CHROMATIN ARRANGEMENTS; RNA-POLYMERASE-II; DE-LANGE-SYNDROME; IN-SITU HYBRIDIZATION; FORMALDEHYDE CROSS-LINKING; LOCAL GENE DENSITY; HIGH-RESOLUTION; SPATIAL-ORGANIZATION;
D O I
10.1128/MMBR.00006-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In humans, nearly two meters of genomic material must be folded to fit inside each micrometer-scale cell nucleus while remaining accessible for gene transcription, DNA replication, and DNA repair. This fact highlights the need for mechanisms governing genome organization during any activity and to maintain the physical organization of chromosomes at all times. Insight into the functions and three-dimensional structures of genomes comes mostly from the application of visual techniques such as fluorescence in situ hybridization (FISH) and molecular approaches including chromosome conformation capture (3C) technologies. Recent developments in both types of approaches now offer the possibility of exploring the folded state of an entire genome and maybe even the identification of how complex molecular machines govern its shape. In this review, we present key methodologies used to study genome organization and discuss what they reveal about chromosome conformation as it relates to transcription regulation across genomic scales in mammals.
引用
收藏
页码:347 / 372
页数:26
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