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RNA maturation transport & localization RNA export to the cytoplasm: model systems RNA degradation Links between RNA processing, transport, degradation RNA localization in the cytoplasm RNA processing: brief overview
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Evidence for checkpoints? mRNA transport All eukaryotic mRNAs are processed
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Specific process for Pol II transcripts nuclear CBC binds to m 7 G-cap: role in splicing, transport, stability (exchanged in cytoplasm) Function in transport, stability, translation 1. Capping
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CPSF: cleavage and polyadenylation specificity factor CStF: cleavage stimulatory factor CF: cleavage factor PAP: polyA polymerase PAB: polyA binding protein Function in transport, stability, translation 2. Polyadenylation
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3. Splicing
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Splicing is mediated by snRNPs
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Compartments inside the nucleus 1. Nucleolus
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2. Perichromatin granule clusters Carter et al., Science (1993) 259: 1330
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Balbiani Rings (Chironomus tentans)
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BR RNP maturation
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BR RNP translocation
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Retroviruses as mRNA export models
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Gene location is influenced by gene activity Casolari et al., 2004
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SUMMARY I.Multiple steps of mRNA biosynthesis are tightly coupled II.Mex67/TAP is one major mRNA export factor Binding to mRNA may already occur at the site of transcription III.Many questions remain - How are mRNA substrates released in the cytoplasm? - Are there multiple mRNA export pathways? - How is processing and transport mechanistically “coupled”? - Is mRNA export regulated? etc.
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RNA half-lives vary greatly but are highly coordinated
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Wang et al., PNAS 2002
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AUUUA element regulates half-life
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A. B. Casein mRNA prolactin + - 30,000 mRNA/cell 300 mRNA/cell No change in transcription Examples of regulated mRNA turnover
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mRNA DEGRADATION mRNA DECAY NMD ‘turnover’‘surveillance’
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mRNA DECAY AAA m7Gppp poly A shorteningDeadenylase complex AAAAAAAAAAAAAAAA m7Gppp DecapitationDecapping enzyme (DCP1 complex) AAA 5’-3’ exonucleolytic cleavageXrn1 complex
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Decay factors localize to cytoplasmic processing bodies (P bodies) Sheth et al. Science 2003
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mRNA activity is regulated by multiple factors Active mRNAsInactive mRNAs Storage Decay Transport Translation
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From Neu-Yilik et al. (2001) EMBO 20:532-540 Position of nonsense codon affects mRNA amounts
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m7Gppp Stop in penultimate exon/ 5’ of splicing mark AAAAAAAAAAAAAAAA DecapitationDecapping enzyme (DCP1 complex) 5’-3’ exonucleolytic cleavageXrn1 complex Nonsense Mediated Decay AAAAAAAAAAAAAAAA
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RNA localization mRNA can be localized to subcellular compartments by actin or tubulin-dependent processes Examples: Xenopus: Vg1 mRNA (TGFb) to vegetal pole Drosophila: nanos, oskar mRNA (posterior) and bicoid (anterior) (requires mRNA binding protein staufen) (requires staufen and miranda) prospero (into ganglion of mother cells; neuroblast TF) Yeast: Ash1 mRNA to daughter cell
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Examples of localized mRNAs in various systems
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lamellipodia stainingperinuclear staining in myotubes 3’ UTR determins localization of many mRNAs
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Bertrand et al., Mol Cell (98) 2:437-445 Ash1 mRNA specifically localizes to new daughter cells
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Mechanism of Ash1 mRNA localization
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SUMMARY I.mRNA decay - regulated and non-regulated turn-over but apparently coordinated - ordered pathways (e.g. deadenylation, decapping, exonucleolytic degradation) - cross-talk between translation and turnover - important regulation via non-coding RNAs - turnover occurs in specific cytoplasmic compartments - NMD: recognition of premature stop codons II.Cytoplasmic mRNA localization - ZIP code in 3’ UTR - both actin and tubulin-mediated - yeast mating type switch as a model: Ash1 mRNA localization (via 3’ UTR, She2/3, Myo4 and actin cables)
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