scholarly journals The isolated catalytic hairpin of the Ras-specific guanine nucleotide exchange factor Cdc25Mmretains nucleotide dissociation activity but has impaired nucleotide exchange activity

FEBS Letters ◽  
2005 ◽  
Vol 579 (30) ◽  
pp. 6851-6858 ◽  
Author(s):  
Elena Sacco ◽  
Sonia Fantinato ◽  
Romilde Manzoni ◽  
David Metalli ◽  
Luca De Gioia ◽  
...  
Keyword(s):  
Guanine Nucleotide Exchange Factor ◽  
Guanine Nucleotide ◽  
Nucleotide Exchange ◽  
Exchange Factor ◽  
Guanine Nucleotide Exchange ◽  
Nucleotide Exchange Factor ◽  
Exchange Activity

scholarly journals Ypt32 recruits the Sec4p guanine nucleotide exchange factor, Sec2p, to secretory vesicles; evidence for a Rab cascade in yeast

2002 ◽  
Vol 157 (6) ◽  
pp. 1005-1016 ◽  
Author(s):  
Darinel Ortiz ◽  
Martina Medkova ◽  
Christiane Walch-Solimena ◽  
Peter Novick
Keyword(s):  
Plasma Membrane ◽  
Guanine Nucleotide Exchange Factor ◽  
Secretory Vesicles ◽  
Guanine Nucleotide ◽  
Nucleotide Exchange ◽  
Exchange Factor ◽  
Guanine Nucleotide Exchange ◽  
Nucleotide Exchange Factor ◽  
Polarized Transport ◽  
Exchange Activity

SEC2 is an essential gene required for polarized growth of the yeast Saccharomyces cerevisiae. It encodes a protein of 759 amino acids that functions as a guanine nucleotide exchange factor for the small GTPase Sec4p, a regulator of Golgi to plasma membrane transport. Activation of Sec4p by Sec2p is needed for polarized transport of vesicles to exocytic sites. Temperature-sensitive (ts) mutations in sec2 and sec4 result in a tight block in secretion and the accumulation of secretory vesicles randomly distributed in the cell. The proper localization of Sec2p to secretory vesicles is essential for its function and is largely independent of Sec4p. Although the ts mutation sec2-78 does not affect nucleotide exchange activity, the protein is mislocalized. Here we present evidence that Ypt31/32p, members of Rab family of GTPases, regulate Sec2p function. First, YPT31/YPT32 suppress the sec2-78 mutation. Second, overexpression of Ypt31/32p restores localization of Sec2-78p. Third, Ypt32p and Sec2p interact biochemically, but Sec2p has no exchange activity on Ypt32p. We propose that Ypt32p and Sec4p act as part of a signaling cascade in which Ypt32p recruits Sec2p to secretory vesicles; once on the vesicle, Sec2p activates Sec4p, enabling the polarized transport of vesicles to the plasma membrane.

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