basic FUNCTION
| cytotoxic granule associated RNA binding protein |
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regulator of alternative pre-mRNA splicing |
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may be involved in induction of apoptosis |
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may have dual role in shuttling between DNA and RNA ligands to co-regulate COL2A1 expression at the level of transcription and pre-mRNA alternative splicing |
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major granule associated species |
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translational silencer of COX2, selectively regulating the expression of TNF |
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nucleolytic activity against cytotoxic lymphocyte target cells |
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acting as a post-transcriptional silencer, and suppressing the production of the TNF-alpha protein |
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TIA1, and TIAL1 are mRNA-binding proteins that can aggregate within granules under specific stress conditions |
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its expression counteracts the inhibitory effect of polypyrimidine tract binding protein, a ubiquitously expressed factor recently implicated in regulation of SMN exon 7 splicing |
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role of TIA1 phosphorylation in autophagy |
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TIA1 oxidation inhibits stress granule assembly and sensitizes cells to stress-induced apoptosis |
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essential contributions of the TIA1 and TIAL1 to the fidelity of mRNA maturation, translation, and RNA-stress-sensing pathways in human cells |
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is an important regulator of the innate immune response in the periphery, dampening cytotoxic inflammation and apoptosis during cellular stress |
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likely TIA1 dampens the immune response in the central nervous system during chronic stress |
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RNA-binding protein that can regulate splicing, stability, or translation of target mRNAs, and play critical roles in stress response and neurodevelopment |
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translation repression is a key process targeted by TIA1 binding which implicate TIA1 function in neuronal differentiation |
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TIA1 appears to control the expression of both pro- and anti-tumorigenic factors in hepatic cancer cells |
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in pro-B cells, the RNA-binding proteins T cell intracellular antigen 1 (TIA1) and TIA1-like protein (TIAL1) act redundantly to enable developmental progression |
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importance of tight regulation of RNA splicing by TIA1 and TIAL1 for the expression of integrative transcriptional programs that control DNA damage sensing and repair during B cell development |
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TIA1 and TIAL1 are key players in the post-transcriptional program that selects high-affinity antigen-specific germinal centers (GCs) B cells |