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PMID: 19217877 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Mitotic chromosome structure: reproducibility of folding and symmetry between sister chromatids.

Biophysical journal ·Vol. 96 ·No. 4 ·2009-02-18 ·Pages 1617-28

Strukov YG, Belmont AS

Abstract

Mitotic chromosome structure and pathways of mitotic condensation remain unknown. The limited amount of structural data on mitotic chromosome structure makes it impossible to distinguish between several mutually conflicting models. Here we used a Chinese hamster ovary cell line with three different lac operator-tagged vector insertions distributed over an approximately 1 microm chromosome arm region to determine positioning reproducibility, long-range correlation in large-scale chromatin folding, and sister chromatid symmetry in minimally perturbed, metaphase chromosomes. The three-dimensional positions of these lac operator-tagged spots, stained with lac repressor, were measured in isolated metaphase chromosomes relative to the central chromatid axes labeled with antibodies to topoisomerase II. Longitudinal, but not axial, positioning of spots was reproducible but showed intrinsic variability, up to approximately 300 nm, between sister chromatids. Spot positions on the same chromatid were uncorrelated, and no correlation or symmetry between the positions of corresponding spots on sister chromatids was detectable, showing the absence of highly ordered, long-range chromatin folding over tens of mega-basepairs. Our observations are in agreement with the absence of any regular, reproducible helical, last level of chromosome folding, but remain consistent with any hierarchical folding model in which irregularity in folding exists at one or multiple levels.

MeSH Terms
Animals Antibodies Antigens, Neoplasm/immunology,metabolism CHO Cells Chromatids/genetics,physiology,ultrastructure Chromosomes, Mammalian/physiology,ultrastructure Computer Simulation Cricetinae Cricetulus DNA Topoisomerases, Type II/immunology,metabolism DNA-Binding Proteins/immunology,metabolism Fluorescent Antibody Technique Image Processing, Computer-Assisted Lac Operon/genetics Metaphase/physiology Microscopy, Fluorescence Repressor Proteins
Chemicals
Antibodies Antigens, Neoplasm DNA-Binding Proteins Repressor Proteins DNA Topoisomerases, Type II
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Strukov Yuri G
Biophysics Program, University of Illinois, Urbana-Champaign, Illinois, USA.
Belmont A S
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
1542-0086
Published
2009-02-18
Pages
1617-28
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC2717231
Subset
IM
Grants
NIGMS NIH HHS · R01 GM042516 · United States
NIGMS NIH HHS · R01 GM42516 · United States
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