Title: RhoRacCdc42
1Rho/Rac/Cdc42
- Dev Bio 231B / Bio Sci D154 (Winter 2008)
- Yi Lecture 3
2System Overview (Arrow Diagram)
FRONT
BACK
3Outline (Yi Lecture 3)
- Ras superfamily and Rho family
- Regulation of actin cytoskeleton and lipid
signaling by Rho family - RhoA protein and the uropod
- Readings
- Xu et al. paper (Figs. 1, 2 and 3)
- Background reading (optional)
- Hall Review on Rho family
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5Small G-Protein (Ras) Superfamily(Monomeric)
- Ras
- Signal transduction (e.g. Ras activates Raf
kinase which activates MAPK signaling) - Rho
- Regulation of cytoskeleton (e.g. Cdc42)
- Rab
- Intracellular vesicular transport (i.e. protein
trafficking) - Arf
- Vesicle coating
- Ran
- Nucleocytoplasmic transport
6Small G-Protein Cycle
Active
GEF
GAP
Inactive
7More Detailed View of G-Protein Cycle
Guanine Dissociation Inhibitor (stabilizes GDP
form)
8Rho Family
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10Rho Family Small G-Proteins Regulate Actin
Organization
Stress fibers contractile bundles of actin and
mysoin II
Lamellipodia 2D sheet-like projections
Filopodia 1D projections
11Rho/Rac/Cdc42 Stimulate Actin Nucleation
Branched
Cables
12Rho/Rac/Cdc42 Regulate Lipid Signaling
13Coordination between Actin Cytoskeleton and Lipids
- Rac/Cdc42 promote formation of PIPs as well as
activating WAVE/WASP which activates Arp2/3 - Many proteins (e.g. profilin) bind both PIPs and
actin - Increases in PIPs leads to enhanced actin
polymerization - Actin stabilizes distribution of PIPs
- Actin and PIPs contribute to the localization of
Rac/Cdc42
14Positive Feedback at Leading Edge
Actin
PIPs
15Rho GEFs
16Rho Effectors
- Rho kinase (ROCK) is a principal effector of Rho
- Rho induces the assembly of contractile
actin-myosin filaments via ROCK - ROCK phosphorylates and inactivates myosin light
chain (MLC) phosphatase which leads to increased
phosphorylation of MLC promoting actin
cross-linking by myosin II - Rho inhibits Rac via ROCK
- ROCK phosphorylates and activates FilGAP (a Rac
GAP) - Rac inhibits Rho by activation of p190RhoGAP
17Tools for Studying Rho Function
- RhoA-GTP pulldown using GST-RBD (Rho Binding
Domain) - RhoA-Q63L constituitively active mutant
- RhoA-T19N dominant negative mutant
- Y-27632 ROCK inhibitor
- PBD-GFP fluorescent probe for Rac-GTP and
Cdc42-GTP
18Figs 1B 1D
19Uniform Distribution Versus Gradient
- How do neutrophils respond when fMLP is applied
in a spatially uniform manner? - Do they move?
- They polarize and move in random directions
20Figure 2
21Figure 3
22Lecture 3 Question to Ponder
2. Neutrophil HL-60 cells are transfected with
the PH-Akt-GFP reporter. One of these cells is
positioned between 2 micropipettes containing
equal concentrations of fMLP. The two
micropipettes are simultaneously turned on
emitting fMLP. DRAW (i.e fill-in) in the cell
where you expect to see the PH-Akt-GFP signal
under the following conditions (1 point
each) Â A) No treatment control (fMLP)
B) Treatment with the Rho
kinase inhibitor Y-27632
23Summary (Yi Lecture 3)
- Rho family of monomeric G-proteins
- Rho, Rac, Cdc42
- Actin polymerization and lipid signaling at
leading edge - Regulated by Rac and Cdc42
- Rho activation inhibits the pseudopod and
promotes the uropod