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PMID: 12975345 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains: evidence for local euchromatic neighborhoods.

The Journal of cell biology ·Vol. 162 ·No. 6 ·2003-09-15 ·Pages 981-90

Shopland LS, Johnson CV, Byron M, McNeil J, Lawrence JB

Abstract

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 ( approximately 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."

MeSH Terms
Cell Line Cell Nucleus/genetics Chromosome Banding Chromosome Structures/genetics Collagen Type I/biosynthesis,genetics DNA Replication/genetics Euchromatin/genetics Eukaryotic Cells/cytology,metabolism Fluorescent Antibody Technique Gene Expression Regulation/genetics Humans Multigene Family/genetics Nuclear Proteins/genetics RNA, Messenger/genetics Ribonucleoproteins Serine-Arginine Splicing Factors
Chemicals
Collagen Type I Euchromatin Nuclear Proteins RNA, Messenger Ribonucleoproteins SRSF2 protein, human Serine-Arginine Splicing Factors
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shopland Lindsay S
Department of Cell Biology, University of Massachusetts Medical Center, Worcester, MA 01655, USA.
Johnson Carol V
Byron Meg
McNeil John
Lawrence Jeanne B
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
2003-09-15
Pages
981-90
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2172856
Subset
IM
Grants
NIGMS NIH HHS · R01 GM053234 · United States
NIGMS NIH HHS · R01 GM068138 · United States
NIGMS NIH HHS · GM53234 · United States
NIGMS NIH HHS · GM68138 · United States
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