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PMID: 12490161 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Evidence that all SC-35 domains contain mRNAs and that transcripts can be structurally constrained within these domains.

Journal of structural biology ·Vol. 140 ·No. 1-3 ·2002-00-00 ·Pages 131-9

Shopland LS, Johnson CV, Lawrence JB

Abstract

A fundamental question of mRNA metabolism concerns the spatial organization of the steps involved in generating mature transcripts and their relationship to SC-35 domains, nuclear compartments enriched in mRNA metabolic factors and poly A+ RNA. Because poly A+ RNA in SC-35 domains remains after transcription inhibition, a prevailing view has been that most or all SC-35 domains do not contain protein-encoding mRNAs but stable RNAs with nuclear functions and thus that these compartments do not have direct roles in mRNA synthesis or transport. However, the transcription, splicing, and transport of transcripts from a specific gene have been shown to occur in association with two of these 15-30 nuclear compartments. Here we show that virtually all SC-35 domains can contain specific mRNAs and that these persist in SC-35 domains after treatment with three different transcription-inhibitory drugs. This suggests perturbation of an mRNA transport step that normally occurs in SC-35 domains and is post-transcriptional but still dependent on ongoing transcription. Finally, even after several hours of transcription arrest, these transcripts do not disperse from SC-35 domains, indicating that they are structurally constrained within them. Our findings importantly suggest a spatially direct role for all SC-35 domains in the coupled steps of mRNA metabolism and transport.

MeSH Terms
Cell Line Cell Nucleus/metabolism Chromatin/metabolism Collagen/biosynthesis Collagen Type I/biosynthesis Collagen Type I, alpha 1 Chain DNA, Complementary/metabolism Humans In Situ Hybridization, Fluorescence Microscopy, Fluorescence Nucleic Acid Hybridization Protein Structure, Tertiary RNA, Messenger/metabolism Ribonucleoproteins, Small Nuclear/metabolism Transcription, Genetic
Chemicals
Chromatin Collagen Type I Collagen Type I, alpha 1 Chain DNA, Complementary RNA, Messenger Ribonucleoproteins, Small Nuclear Collagen
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Shopland Lindsay S
Department of Cell Biology, University of Massachusetts Medical School, 55 Lake Avenue North (S3-138), Worcester, MA 01655-0002, USA.
Johnson Carol V
Lawrence Jeanne B
Article Info
Journal
Journal of structural biology
Abbr.
J Struct Biol
ISSN
1047-8477
Published
2002-00-00
Pages
131-9
Language
English
Region
United States
NLM ID
9011206
Subset
IM
Grants
NIGMS NIH HHS · GM18846 · United States
NIGMS NIH HHS · GM49254 · United States
NIGMS NIH HHS · GM53234 · United States
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