scholarly journals Microinjection of recombinant p21rho induces rapid changes in cell morphology.

1990 ◽  
Vol 111 (3) ◽  
pp. 1001-1007 ◽  
Author(s):  
H F Paterson ◽  
A J Self ◽  
M D Garrett ◽  
I Just ◽  
K Aktories ◽  
...  

The rho proteins, p21rho, are ubiquitously expressed guanine nucleotide binding proteins with approximately 30% amino acid homology to p21ras, but their biochemical function is unknown. We show here that microinjection of constitutively activated recombinant rho protein (Val14rho) into subconfluent cells induces dramatic changes in cell morphology: 15-30 min after injection cells adopt a distinct and novel phenotype with a contracted cell body and finger-like processes still adherent to the substratum. Ribosylation of Val14rho with the ADP-ribosyltransferase C3 from clostridium botulinum, before microinjection, renders the protein biologically inactive, but it has no effect on either its intrinsic biochemical properties or on its interaction with the GTPase activating protein, rho GAP. Micro-injection of ribosylated normal rho, on the other hand, has a similar effect of injection of C3 transferase and induces complete rounding up of cells. We also report striking biochemical changes in actin filament organization when contact-inhibited quiescent 3T3 cells are injected with Val14rho protein. The effects induced by activation or inactivation of p21rho described here, suggest that the biological function of this protein is to control some aspect of cytoskeletal organization.

2011 ◽  
Vol 392 (8-9) ◽  
pp. 791-797 ◽  
Author(s):  
Eldar Zent ◽  
Ingrid Vetter ◽  
Alfred Wittinghofer

Abstract Septins constitute a family of conserved guanine nucleotide binding proteins found in a wide range of organisms from fungi to mammals. Members of the family share a canonical G-domain with N- and C-terminal extensions. G-domains assemble into hetero-oligomeric complexes which form non-polarised filaments or rings. Linear filaments are formed between the G-domains using either the guanine nucleotide binding site (G interface) or N- and C-terminal extensions (NC interface). Sept7 is a unique among the 13 human septins in that it occupies the ends of hexameric building blocks which assemble into non-polarised filaments. To gain insight into its particular properties we performed structural and biochemical studies on Sept7. We solved the crystal structure of a Sept7 dimer in the GDP-bound state. The structure and biochemistry of Sept7 provide new insights into the dynamics of the G interface and outline the differences in the properties of Sept7 compared to the members of group 2 septins.


FEBS Letters ◽  
1986 ◽  
Vol 199 (1) ◽  
pp. 103-106 ◽  
Author(s):  
Peter Gierschik ◽  
Bernice Morrow ◽  
Graeme Milligan ◽  
Charles Rubin ◽  
Allen Spiegel

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