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PMID: 21131981 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Validation Study

The three-dimensional folding of the α-globin gene domain reveals formation of chromatin globules.

Nature structural & molecular biology ·Vol. 18 ·No. 1 ·2011-01-00 ·Pages 107-14

Baù D, Sanyal A, Lajoie BR, Capriotti E, Byron M, Lawrence JB, Dekker J, Marti-Renom MA

Abstract

We developed a general approach that combines chromosome conformation capture carbon copy (5C) with the Integrated Modeling Platform (IMP) to generate high-resolution three-dimensional models of chromatin at the megabase scale. We applied this approach to the ENm008 domain on human chromosome 16, containing the α-globin locus, which is expressed in K562 cells and silenced in lymphoblastoid cells (GM12878). The models accurately reproduce the known looping interactions between the α-globin genes and their distal regulatory elements. Further, we find using our approach that the domain folds into a single globular conformation in GM12878 cells, whereas two globules are formed in K562 cells. The central cores of these globules are enriched for transcribed genes, whereas nontranscribed chromatin is more peripheral. We propose that globule formation represents a higher-order folding state related to clustering of transcribed genes around shared transcription machineries, as previously observed by microscopy.

MeSH Terms
Chromatin/chemistry,ultrastructure Chromosomes, Human, Pair 16/chemistry,metabolism,ultrastructure Humans In Situ Hybridization, Fluorescence K562 Cells Models, Molecular Nucleic Acid Conformation alpha-Globins/chemistry,genetics
Chemicals
Chromatin alpha-Globins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Baù Davide
Structural Genomics Unit, Bioinformatics and Genomics Department, Centro de Investigación Príncipe Felipe, Valencia, Spain.
Sanyal Amartya
Lajoie Bryan R
Capriotti Emidio
Byron Meg
Lawrence Jeanne B
Dekker Job
Marti-Renom Marc A
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Article Info
Journal
Nature structural & molecular biology
Abbr.
Nat Struct Mol Biol
ISSN
1545-9985
Published
2011-01-00
Epub
2010-00-05
Pages
107-14
Language
English
Region
United States
NLM ID
101186374
PMCID
PMC3056208
Subset
IM
Grants
NHGRI NIH HHS · HG003143 · United States
NHGRI NIH HHS · R01 HG003143 · United States
NIGMS NIH HHS · GM053234 · United States
NIGMS NIH HHS · R01 GM053234 · United States
NHGRI NIH HHS · R01 HG003143-06 · United States
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