PubMed ID

14617810

UMMS Affiliation

Department of Cell Biology

Date

11-18-2003

Document Type

Article

Subjects

Animals; Cell Differentiation; Cell Nucleus; Cells, Cultured; Chick Embryo; Chromatin; Humans; In Situ Hybridization, Fluorescence; Mice; Microscopy, Fluorescence; Muscle Development; MyoD Protein; Myoblasts; Myogenin; NIH 3T3 Cells; Protein Subunits; Ventricular Myosins

Disciplines

Cell Biology | Life Sciences | Medicine and Health Sciences

Abstract

Previous studies have shown that in a given cell type, certain active genes associate with SC-35 domains, nuclear regions rich in RNA metabolic factors and excluded from heterochromatin. This organization is not seen for all active genes; therefore, it is important to determine whether and when this locus-specific organization arises during development and differentiation of specific cell types. Here, we investigate whether gene organization relative to SC-35 domains is cell type specific by following several muscle and nonmuscle genes in human fibroblasts, committed but proliferative myoblasts, and terminally differentiated muscle. Although no change was seen for other loci, two muscle genes (Human beta-cardiac myosin heavy chain and myogenin) became localized to the periphery of an SC-35 domain in terminally differentiated muscle nuclei, but not in proliferative myoblasts or in fibroblasts. There was no apparent change in gene localization relative to either the chromosome territory or the heterochromatic compartment; thus, the gene repositioning seemed to occur specifically with respect to SC-35 domains. This gene relocation adjacent to a prominent SC-35 domain was recapitulated in mouse 3T3 cells induced into myogenesis by introduction of MyoD. Results demonstrate a cell type-specific reorganization of specific developmentally regulated loci relative to large domains of RNA metabolic factors, which may facilitate developmental regulation of genome expression.

Rights and Permissions

Citation: Mol Biol Cell. 2004 Jan;15(1):197-206. Epub 2003 Nov 14. Link to article on publisher's site

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Link to Article in PubMed