Typically, eukaryotic nuclei contain 10–30 prominent domains (referred to here as SC-35 domains) that are concentrated in mRNA metabolic factors. Here, we show that multiple specific genes cluster around a common SC-35 domain, which contains multiple mRNAs. Nonsyntenic genes are capable of associating with a common domain, but domain “choice” appears random, even for two coordinately expressed genes. Active genes widely separated on different chromosome arms associate with the same domain frequently, assorting randomly into the 3–4 subregions of the chromosome periphery that contact a domain. Most importantly, visualization of six individual chromosome bands showed that large genomic segments (∼5 Mb) have striking differences in organization relative to domains. Certain bands showed extensive contact, often aligning with or encircling an SC-35 domain, whereas others did not. All three gene-rich reverse bands showed this more than the gene-poor Giemsa dark bands, and morphometric analyses demonstrated statistically significant differences. Similarly, late-replicating DNA generally avoids SC-35 domains. These findings suggest a functional rationale for gene clustering in chromosomal bands, which relates to nuclear clustering of genes with SC-35 domains. Rather than random reservoirs of splicing factors, or factors accumulated on an individual highly active gene, we propose a model of SC-35 domains as functional centers for a multitude of clustered genes, forming local euchromatic “neighborhoods.”
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15 September 2003
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September 15 2003
Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains : evidence for local euchromatic neighborhoods
Lindsay S. Shopland,
Lindsay S. Shopland
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
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Carol V. Johnson,
Carol V. Johnson
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
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Meg Byron,
Meg Byron
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
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John McNeil,
John McNeil
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
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Jeanne B. Lawrence
Jeanne B. Lawrence
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
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Lindsay S. Shopland
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
Carol V. Johnson
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
Meg Byron
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
John McNeil
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
Jeanne B. Lawrence
Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655
Address correspondence to Jeanne Lawrence, Dept. of Cell Biology, University of Massachusetts Medical Center, 55 Lake Avenue North, Worcester, MA 01655. Tel.: (508) 856-6015. Fax: (508) 856-5178. email: [email protected]
The online version of this article includes supplemental material.
L.S. Shopland's present address is The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609.
Abbreviations used in this paper: ACTB, β-actin; COL1A1, collagen type 1, α1; COL1A2, collagen type 1, α2; G-band, Giemsa dark band; R-band, reverse band.
Received:
March 19 2003
Accepted:
August 04 2003
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 162 (6): 981–990.
Article history
Received:
March 19 2003
Accepted:
August 04 2003
Citation
Lindsay S. Shopland, Carol V. Johnson, Meg Byron, John McNeil, Jeanne B. Lawrence; Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains : evidence for local euchromatic neighborhoods . J Cell Biol 15 September 2003; 162 (6): 981–990. doi: https://doi.org/10.1083/jcb.200303131
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