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Published byTimothy Boone Modified over 9 years ago
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RNA localization mRNA can be localized to subcellular compartments by actin or tubulin-dependent processes Examples: Xenopus: Vg1 mRNA (TGF ) 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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lamellipodia stainingperinuclear staining in myotubes
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Bertrand et al., Mol Cell (98) 2:437-445
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SUMMARY 2 I.mRNA decay - regulated and non-regulated turn-over - ordered pathway (deadenylation, decapping, exonucleolytic degradation) - 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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ER translocation & vesicular transport
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from: Jamieson and Palade 3min 7min 37min117min
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In vitro reconstitution of ER translocation: - Sec61 complex: conserved translocation channel Sec61 subunits ( ) Sec62/63 TRAM (translocating chain-assoc. membrane protein) - phospholipids (proteoliposomes) and luminal chaperones (BIP) - SRP/SRP receptor only required for co-translational translocation not for post-translational translocation (e.g pre-pro-alpha factor). - energetics of translocation: protein conducting channel (cotranslational) molecular ratcheting (posttranslational)
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Probing of translocation intermediates with fluorescent peptides From: Liao and Johnson Cell (97)
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The Sec61 complex forms a channel Menetret et al. Mol Cell (2000) 6:1219
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From: Beckmann et al. Cell (2001) Vol 107, 361-372
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From: Van den Berg et al. Nature (2004) 427, 36-44
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Topology of membrane-spanning proteins
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Type I membrane proteins have a cleavable signal sequence
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Type II membrane proteins have internal signal sequence
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Type III membrane proteins have internal signal sequence
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Type II+III membrane proteins have internal signal sequences
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From: Beckmann et al. Cell (2001) Vol 107, 361-372
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Translocation of proteins with multiple membrane spanning domains
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From: Van den Berg et al. Nature (2004) 427, 36-44
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Formation of a glycosylphosphatidylinositol (GPI)-anchor
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ER function - Proper folding of proteins (chaperones, lectins, petidyl-prolyl-isomerases) - Formation of disulfide bonds (PDI) GSH prevents oxidation in cytosol GS-SG + NADPH + H + 2 GSH + NADP + - Proteolytic cleavages - Addition & processing of carbohydrates - Assembly into multimeric proteins - Ca2+ storage - Lipid synthesis - Detoxification (liver!)
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Folding of Influenza hemagglutinin (HA)
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Ser/Thr
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Summary ER translocation: SRP-dependent and -independent pathways; translocation occurs through Sec61 complex; topogenic sequences determine overall orientation. ER function Compartmental identity: maturation versus fixed compartments Identification of components: combination of genetics, biochemistry... Vesicular coats: COPI ~ retrograde: Golgi->ER COPII ~anterograde: ER->Golgi CCV post-Golgi, various adaptors
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