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Mol Cell Biol. 2011 Mar;31(5):935-54. doi: 10.1128/MCB.00945-10. Epub 2010 Dec 28.

TIA1 prevents skipping of a critical exon associated with spinal muscular atrophy.

Author information

1
Department of Biomedical Sciences, College of Veterinary Medicine, 2034 Veterinary Medicine Bldg., Iowa State University, Ames, IA 50011, USA. singhr@iastate.edu

Abstract

Prevention of skipping of exon 7 during pre-mRNA splicing of Survival Motor Neuron 2 (SMN2) holds the promise for cure of spinal muscular atrophy (SMA), a leading genetic cause of infant mortality. Here, we report T-cell-restricted intracellular antigen 1 (TIA1) and TIA1-related (TIAR) proteins as intron-associated positive regulators of SMN2 exon 7 splicing. We show that TIA1/TIAR stimulate exon recognition in an entirely novel context in which intronic U-rich motifs are separated from the 5' splice site by overlapping inhibitory elements. TIA1 and TIAR are modular proteins with three N-terminal RNA recognition motifs (RRMs) and a C-terminal glutamine-rich (Q-rich) domain. Our results reveal that any one RRM in combination with a Q domain is necessary and sufficient for TIA1-associated regulation of SMN2 exon 7 splicing in vivo. We also show that increased expression of TIA1 counteracts the inhibitory effect of polypyrimidine tract binding protein, a ubiquitously expressed factor recently implicated in regulation of SMN exon 7 splicing. Our findings expand the scope of TIA1/TIAR in genome-wide regulation of alternative splicing under normal and pathological conditions.

PMID:
21189287
PMCID:
PMC3067828
DOI:
10.1128/MCB.00945-10
[Indexed for MEDLINE]
Free PMC Article
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