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PMID: 15519694 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Internal organisation of the nucleus: assembly of compartments by macromolecular crowding and the nuclear matrix model.

Biology of the cell ·Vol. 96 ·No. 8 ·2004-10-00 ·Pages 595-601

Hancock R

Abstract

Many and possibly all macromolecules in the nucleus are segregated into discrete compartments, but the current model that this is achieved by a fibrillar nuclear matrix which structures the nuclear interior and compartments is not consistent with all experimental observations, as reviewed here. New results are presented which suggest that macromolecular crowding forces play a crucial role in the assembly of at least two compartments, nucleoli and PML bodies, and an in vitro system in which crowding assembles macromolecular complexes into structures which resemble nuclear compartments is described. Crowding forces, which are strong in the nucleus due to the high macromolecule concentration (in the range of 100 mg/ml), vastly increase the association constants of intermolecular interactions and can segregate different macromolecules into discrete phases. The model that they play a role in compartmentalisation of the nucleus is generally consistent with the properties of compartments, including their spherical or quasispherical form and their dynamic and mobile nature.

MeSH Terms
Animals Cell Nucleolus/metabolism Cell Nucleus/drug effects,physiology,ultrastructure DNA/metabolism Humans Hypotonic Solutions/pharmacology Intranuclear Space/metabolism Macromolecular Substances/chemistry,metabolism Matrix Attachment Regions/physiology Models, Biological Neoplasm Proteins/metabolism Nuclear Matrix/chemistry,physiology Nuclear Matrix-Associated Proteins/metabolism,physiology Nuclear Proteins/chemistry,metabolism Promyelocytic Leukemia Protein Thermodynamics Transcription Factors/metabolism Tumor Suppressor Proteins
Chemicals
Hypotonic Solutions Macromolecular Substances Neoplasm Proteins Nuclear Matrix-Associated Proteins Nuclear Proteins Promyelocytic Leukemia Protein Transcription Factors Tumor Suppressor Proteins PML protein, human DNA
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Hancock Ronald
Laval University Cancer Research Centre, Hôtel-Dieu Hospital, 9 rue MacMahon, Quebec, P.Q. G1R 2J6, Canada. ronald.hancock@crhdq.ulaval.ca
Article Info
Journal
Biology of the cell
Abbr.
Biol Cell
ISSN
0248-4900
Published
2004-10-00
Pages
595-601
Language
English
Region
England
NLM ID
8108529
Subset
IM
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