A yeast two-hybrid screen revealed that regulatory subunits (RII) of PKAII bind the Yotiao protein. Yotiao interacts with the NR1 subunit of the NMDA receptor. A purified C-terminal fragment of Yotiao binds PKAII, via an RII binding site constituted by amino acid residues 1452-1469, with a dissociation constant (K(d)) between 50 and 90 nM in vitro. A stable complex composed of Yotiao, RII and NR1 was immunoprecipitated from whole rat brain extracts. Immunostaining analysis disclosed that Yotiao, RIIbeta and NR1 colocalize in striatal and cerebellar neurons. Co-assembly of Yotiao/PKAII complexes with NR1 subunits may promote cAMP-dependent modulation of NMDA receptor activity at synapses, thereby influencing brain development and synaptic plasticity.
Yotiao protein, a ligand for the NMDA receptor, binds and targets cAMP-dependent protein kinase II / Feliciello, Antonio; Cardone, Luca; Garbi, Corrado; Ginsberg, Md; Varrone, Stelio; Rubin, Cs; Avvedimento, VITTORIO ENRICO; Gottesman, M. E.. - In: FEBS LETTERS. - ISSN 0014-5793. - STAMPA. - 464:(1999), pp. 174-178.
Yotiao protein, a ligand for the NMDA receptor, binds and targets cAMP-dependent protein kinase II
FELICIELLO, ANTONIO;CARDONE, LUCA;GARBI, CORRADO;VARRONE, STELIO;AVVEDIMENTO, VITTORIO ENRICO;
1999
Abstract
A yeast two-hybrid screen revealed that regulatory subunits (RII) of PKAII bind the Yotiao protein. Yotiao interacts with the NR1 subunit of the NMDA receptor. A purified C-terminal fragment of Yotiao binds PKAII, via an RII binding site constituted by amino acid residues 1452-1469, with a dissociation constant (K(d)) between 50 and 90 nM in vitro. A stable complex composed of Yotiao, RII and NR1 was immunoprecipitated from whole rat brain extracts. Immunostaining analysis disclosed that Yotiao, RIIbeta and NR1 colocalize in striatal and cerebellar neurons. Co-assembly of Yotiao/PKAII complexes with NR1 subunits may promote cAMP-dependent modulation of NMDA receptor activity at synapses, thereby influencing brain development and synaptic plasticity.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.