Affiliation:
1. Laboratory of Cellular and Molecular Biology
2. Research Resources Branch
3. Laboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health,
Baltimore, Maryland 21224
Abstract
ABSTRACT
The
RNA-binding protein TIA-1 (T-cell intracellular antigen 1) functions as
a posttranscriptional regulator of gene expression and aggregates to
form stress granules following cellular damage. TIA-1 was previously
shown to bind mRNAs encoding tumor necrosis factor alpha
(TNF-α) and cyclooxygenase 2 (COX-2), but TIA-1 target mRNAs
have not been systematically identified. Here, immunoprecipitation (IP)
of TIA-1-RNA complexes, followed by microarray-based
identification and computational analysis of bound transcripts, was
used to elucidate a common motif present among TIA-1 target mRNAs. The
predicted TIA-1 motif was a U-rich, 30- to 37-nucleotide (nt)-long
bipartite element forming loops of variable size and a bent stem. The
TIA-1 motif was found in the
TNF-α
and
COX-2
mRNAs and in 3,019 additional UniGene transcripts (∼3% of the
UniGene database), localizing preferentially to the 3′
untranslated region. The interactions between TIA-1 and target
transcripts were validated by IP of endogenous mRNAs, followed by
reverse transcription and PCR-mediated detection, and by pulldown of
biotinylated RNAs, followed by Western blotting. Further studies using
RNA interference revealed that TIA-1 repressed the
translation of bound mRNAs. In summary, we report a signature motif
present in mRNAs that associate with TIA-1 and provide support to the
notion that TIA-1 represses the translation of target
transcripts.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
205 articles.
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