Sites of phosphorylation by protein kinase a in CDC25Mm/GRF1, a guanine nucleotide exchange factor for Ras

S Baouz (1) , E Jacquet (1) , K Accorsi (1) , C Hountondji (1) , M Balestrin (1) , R Zippel (1) , E Sturani (1) , A Parmeggiani (2, 3)

1 Groupe de Biophysique
2 BIOC - Laboratoire de Biochimie de l'Ecole polytechnique
3 Dipartimento Fisiol e Biochim Gen

Activation of the neuronal Ras GDP/GTP exchange factor (GEF) CDC25Mm/GRF1 is known to be associated with phosphorylation of serine/threonine. To increase our knowledge of the mechanism involved, we have analyzed the ability of several serine/threonine kinases to phosphorylate CDC25Mm in vivo and in vitro. We could demonstrate the involvement of cAMP-dependent protein kinase (PKA) in the phosphorylation of CDC25Mm in fibroblasts overexpressing this RasGEF as well as in mouse brain synaptosomal membranes. In vitro, PKA was found to phosphorylate multiple sites on purified CDC25Mm, in contrast to protein kinase C, calmodulin kinase II, and casein kinase II, which were virtually inactive. Eight phosphorylated serines and one threonine were identified by mass spectrometry and Edman degradation. Most of them were clustered around the Ras exchanger motif/PEST motifs situated in the C-terminal moiety (residues 631-978) preceding the catalytic domain. Ser(745) and Ser(822) were the most heavily phosphorylated residues and the only ones coinciding with PKA consensus sequences. Substitutions S745D and S822D showed that the latter mutation strongly inhibited the exchange activity of CDC25Mm on Ha-Ras. The multiple PKA-dependent phosphorylation sites on CDC25Mm suggest a complex regulatory picture of this RasGEF. The results are discussed in the light of structural and/or functional similarities with other members of this RasGEF family.

Domains: Life Sciences [q-bio]; Biochemistry, Molecular Biology

S Baouz, E Jacquet, K Accorsi, C Hountondji, M Balestrin, et al.. Sites of phosphorylation by protein kinase a in CDC25Mm/GRF1, a guanine nucleotide exchange factor for Ras. Journal of Biological Chemistry, 2001, 276 (3), pp.1742. ⟨hal-00771803⟩