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S1‐1 nuclear domains: characterization and dynamics as a function of transcriptional activity
Author(s) -
Inoue Akira,
Tsugawa Katsuji,
Tokunaga Kazuaki,
Takahashi Kenichi P.,
Uni Shigehiko,
Kimura Masatsugu,
Nishio Koji,
Yamamoto Naoki,
Honda Kenichi,
Watanabe Takanori,
Yamane Hideo,
Tani Tokio
Publication year - 2008
Publication title -
biology of the cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 85
eISSN - 1768-322X
pISSN - 0248-4900
DOI - 10.1042/bc20070142
Subject(s) - nucleoplasm , biology , immunoelectron microscopy , cell nucleus , rna , microbiology and biotechnology , transcription (linguistics) , nuclear protein , messenger rna , gene expression , cajal body , nucleolus , rna polymerase ii , rna splicing , transcription factor , gene , cytoplasm , genetics , promoter , linguistics , philosophy , antibody
Background information . The RNA‐binding protein S1‐1, also called RBM10 (RNA‐binding motif 10), is a paralogue of putative tumour suppressor RBM5 and has been correlated with cancer proliferation and apoptosis. In the present study, we have investigated the cell biology of S1‐1. Results . In the extranucleolar nucleoplasm, S1‐1 occurred in hundreds of punctate and irregular domains. Some 10–40 of these domains were larger than 0.5 μm and prominent for S1‐1 immunostaining. These domains (S1‐1 nuclear bodies) were commonly present in tissue cells and in cultured cells. When cellular transcription was globally reduced by heat shock, serum starvation, culture at high cell densities or inhibition with RNA polymerase II inhibitors, small S1‐1 domains (S1‐1 granules), with weak immunostaining signals, reduced in number, whereas S1‐1 nuclear bodies became prominent and increased in size. These altered S1‐1 domains were returned to initial states when the cells were placed under normal conditions. Similar to paraspeckles, S1‐1 nuclear bodies occurred closely adjacent to nuclear speckles or IGCs (interchromatin granule clusters), as determined by immunoelectron microscopy. However, the S1‐1 nuclear bodies did not correspond to paraspeckles or IGAZs (interchromatin‐granule‐associated zones), but coincided with TIDRs (transcription‐inactivation‐dependent RNA domains), which we had characterized previously at the RNA level. The enlarged S1‐1 nuclear bodies/TIDRs accumulated the S1‐1 protein and microinjected primary and spliced mRNAs, presumably for later elevation of gene expression. In addition, electron microscopy revealed that S1‐1 was also present on perichromatin fibrils, suggesting the structure of S1‐1 granules seen at higher resolution. Conclusions . S1‐1 constitutes hundreds of nuclear domains, which dynamically change their structures in a reversible manner. Upon globally reducing RNA polymerase II transcription, S1‐1 nuclear bodies enlarge and decrease in number. They are novel domains different from paraspeckles or IGAZs, despite their similar occurrence adjacent to nuclear speckles. We discuss S1‐1 granules in terms of their association with gene expression. In addition, this is the first report of a TIDR‐localized protein.