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PMID: 22703176 Published · ppublish English Journal Article Review

Methods for identifying higher-order chromatin structure.

Annual review of genomics and human genetics ·Vol. 13 ·2012-00-00 ·Pages 59-82

Sajan SA, Hawkins RD

Abstract

Eukaryotic genomic DNA is combined with histones, nonhistone proteins, and RNA to form chromatin, which is extensively packaged hierarchically to fit inside a cell's nucleus. The nucleosome-comprising a histone octamer with 147 base pairs of DNA wrapped around it-is the initial level and the repeating unit of chromatin packaging, which electron microscopy first made visible to the human eye as "beads on a string" nearly four decades ago. The mechanism and nature of chromatin packaging are still under intense research. Recently, classic methods like chromatin immunoprecipitation and digestion with deoxyribonuclease and micrococcal nuclease have been combined with high-throughput sequencing to provide detailed nucleosome occupancy maps, and chromosome conformation capture and its variants have revealed that higher-order chromatin structure involves long-range loop formation between distant genomic elements. This review discusses the methods for identifying higher-order chromatin structure and the information they have provided on this important topic.

MeSH Terms
Animals Chromatin/chemistry,genetics,metabolism Chromatin Immunoprecipitation DNA Cleavage Epistasis, Genetic Gene Expression Regulation Histones/chemistry,metabolism Humans Models, Molecular Nucleic Acid Conformation Protein Conformation Sequence Analysis, DNA
Chemicals
Chromatin Histones
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sajan Samin A
Department of Medicine, Division of Human Genetics, University of Washington, Seattle, WA 98195, USA.
Hawkins R David
Article Info
Journal
Annual review of genomics and human genetics
Abbr.
Annu Rev Genomics Hum Genet
ISSN
1545-293X
Published
2012-00-00
Epub
2012-00-06
Pages
59-82
Language
English
Region
United States
NLM ID
100911346
Subset
IM
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