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RIC-8 is Required for GPR-1/2 Dependent G Function During Asymmetric Division of C.elegans embryos Colombo K., Johnston C.A., McCudden C.R., Sidervoski D.P. and Grönczy P. Cell, Vol. 119, 219-230 Colombo K., Johnston C.A., McCudden C.R., Sidervoski D.P. and Grönczy P. Cell, Vol. 119, 219-230
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Background G-Proteins are heterotrimeric protein complexs…G + (G +G ) = G protein Ligand binding to GCPR activates G- proteins… G-Proteins are heterotrimeric protein complexs…G + (G +G ) = G protein Ligand binding to GCPR activates G- proteins…
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G-protein coupled receptors
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Heterotrimeric G protein cycle GEF (ligand-bound receptor) GAP (RGS) “ON” “OFF” ©2002 Lee Bardwell
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What does G do next ? Adenylate Cyclase ©2002 Lee Bardwell
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Background G-Proteins are heterotrimeric protein complexs…G + (G +G ) = G protein Ligand binding to GCPR activates G- proteins… Many types of G-proteins made of different sub-unit compositions all with different effectors. Interested in GOA-1 and GPA-16 G-Proteins are heterotrimeric protein complexs…G + (G +G ) = G protein Ligand binding to GCPR activates G- proteins… Many types of G-proteins made of different sub-unit compositions all with different effectors. Interested in GOA-1 and GPA-16
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In One Cell embryos…it works much differently Experimental evidence has shown that …. 1) G-pro’s activate without GCPR 2) Single cell cleavage involves a GoLoco protein GPR1/2- a GDI The hypothesis is that.. G -GDP mediates spindle elongation not G -GTP Two G proteins… GOA-1 and GPA-16
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Experimental Question and Significance What are the mechanisms regulating G-protein mediated pulling forces from Spindles Do other proteins get involved? What are the mechanisms regulating G-protein mediated pulling forces from Spindles Do other proteins get involved? RIC-8 -Thought to positively regulate G activity -Mutants show abnormal spindle formation
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The story… Where is Ric-8? RIC-8 Functions? What are RIC-8 and GPR-1/2 Role of G Subunits? Functional model Where is Ric-8? RIC-8 Functions? What are RIC-8 and GPR-1/2 Role of G Subunits? Functional model
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Results…RIC-8 distribution RIC-8 = Red Tubulin = Green DNA= Blue
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RIC-8 distribution Mutant strains don’t produce null ric-8 embryos ric-8 RNAi gives a more intense knock down
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RIC-8 distribution Interfering with goa-1 and gpa-16 doesn’t effect RIC-8 distribution. Conclusion: RIC-8 is primarily found in Cytoplasm a bit in the cortex and peri-nuclear area
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Results….RIC-8 required for asymmetric division Ric-8 RNAi + mutant equals strongest effect
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Movies… 1.Wild type first cell division 2.Ric-8 RNAi first cell division
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ric-8 is required for pulling forces Focus on the loss of asymmetry…not so much The overall reduction
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RIC-8 interacts with GOA-1 and GPA-16…In vitro Ric-8(md303) = AA substitution at conserved residue (A275E) Ric-8(md1909)= deletion of AA b/w 193-249 Constructs didn’t bind either Intragenic revertant ric-8(md1712 md303) rescued binding
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RIC-8 interacts with GOA-1 and GPA-16…In vivo Coimmunoprecipitation Lack of RIC-8 GOA-1 Coprecip. In Mutant strains Why no binding to to GPA-1/2?? Where is GPA-16??
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RIC-8 is a GEF…GPR-1/2 a GDI Biochemical GTP S assay RIC-8 prefers GOA-1-GDP Increase in RIC-8 = Increase In GTP S binding…. RIC-8 is a GEF RIC-8 increases the G-Protein Cycle GPR-1/2 inhibits RIC-8 Association with GOA-1
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HOW are a GEF and a GDI working together to activate a G subunit?
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RIC-8 necessary for GOA-1/ GPR1/2 interaction GPR-1/2 GOA-1 association Is not required for RIC-8 binding To GOA-1… THE REVERSE RIC-8 GOA-1 binding is required for GPR-1/2 binding To GOA-1 RIC-8 acts on GOA-1 before GPR-1/2
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GDI affects the GEF Kinetics Now this graph makes sense…
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Role of G
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G inactivation alleviates RIC-8 requirement RIC-8 works by increasing the rate of G-pro cycle Knocking down the G is going to do the same thing More free G
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G inactivation alleviates RIC-8 requirement Epistasis assay GPB function is Epistatic to RIC-8
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The final model
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Some Questions What happened to GPA-16? How does the RGS in the model fit in your experimental data? Why can’t GPR-1/2 act on G -GDP as soon as it is dissociated from G-protein complex? What happened to GPA-16? How does the RGS in the model fit in your experimental data? Why can’t GPR-1/2 act on G -GDP as soon as it is dissociated from G-protein complex?
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Question But they are both Asymmetric?
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