G-protein from Medicago sativa: Functional association to photoreceptors

MUSCHIETTI, J.P.; MARTINETTO, H.E.; COSO, O.A.; FARBER, M.D.; TORRES, H.N.; FLAWIA, M.M.

BIOCHEMICAL JOURNAL

PORTLAND PRESS LTD

Año: 1993 vol. 291 p. 383 - 388

0264-6021

G-protein subunits were characterized from Medicago sativa (alfalfa) seedlings. Crude membranes and GTP-Sepharose-purified fractions were electrophoresed on SDS/polyacrylamide gels and analysed by Western blotting with 9193 (anti-α(common)) and AS/7 (anti-α(t), anti-α(i1) and anti α(i2)) polyclonal antibodies. These procedures led to the identification of a specific polypeptide band of about 43 kDa. Another polypeptide reacting with the SW/1 (anti-β) antibody, of about 37 kDa, was also detected. The 43 kDa polypeptide bound specifically [α-32P]GTP by a photoaffinity reaction and was ADP-ribosylated by activated cholera toxin, but not by pertussis toxin. Irradiation of etiolated Medicago sativa protoplast preparations at 660 nm for 1 min produced a maximal increase in the guanosine 5´-[γ-thio]triphosphate (GTP[35S])-binding rate. After this period of irradiation, the binding rate tended to decrease. The effect of a red-light (660 nm) pulse on the binding rate was reversed when it was immediately followed by a period of far-red (> 730 nm) illumination. These results may suggest that activation of GTP[S]binding rate was a consequence of conversion of phytochrome P(r) into the P(f)r form.