THE NOVEL CYCLIC DINUCLEOTIDE 3'-5'-CYCLIC-DIGUANYLIC ACID BINDS TO P21(RAS) AND ENHANCES DNA-SYNTHESIS BUT NOT CELL REPLICATION IN THE MOLT 4 CELL-LINE
D. Amikam et al., THE NOVEL CYCLIC DINUCLEOTIDE 3'-5'-CYCLIC-DIGUANYLIC ACID BINDS TO P21(RAS) AND ENHANCES DNA-SYNTHESIS BUT NOT CELL REPLICATION IN THE MOLT 4 CELL-LINE, Biochemical journal, 311, 1995, pp. 921-927
1. The effect of the novel, naturally occurring nucleotide 3 '-5 ' cyc
lic diguanylic acid (c-di-GMP) on the lymphoblastoid Molt 4 cell line
was studied, When exposed to this guanine nucleotide, Molt 4 cells exh
ibited a marked increase in [H-3]thymidine incorporation, up to 200-fo
ld at 50 mu M c-di-GMP. Correspondingly, the DNA content of the treate
d cells was 9-fold higher th;ln untreated cells. Stimulation of [H-3]t
hymidine incorporation into the cells was time- and concentration-depe
ndent. This effect was specific and was not observed with GMP or cycli
c GMP, nor with the unhydrolysable GTP analogues, guanosine 5 '-[gamma
-thio]triphosphate and guanosine 5 '-[beta gamma-imido]triphosphate. C
-di-GMP entrance into the cells was experimentally verified and occurr
ed without using any means of cell permeabilization. SDS/PAGE analysis
of cells exposed to [P-32]c-di-GMP, followed by autoradiography, reve
aled the labelling of three low-molecular-mass proteins at 18-27 kDa.
The labelling is highly specific to c-di-GMP and its extent was not af
fected by other guanine nucleotides. 2. One of the c-di-GMP-binding pr
oteins was found to be the p21(ras) protein, by immunoprecipitation wi
th the anti-Ras monoclonal antibody Y13-259. The effects described app
ear to be unique for c-di-GMP and, taken together, raise the possibili
ty that an irreversible binding of this guanine nucleotide to the grow
th-promoting p21(ras) protein results in a fixed active conformation o
f this protein affecting DNA synthesis. Strikingly, although at 48 h o
f growth markedly high DNA levels were found in Molt 4 cells treated w
ith c-di-GMP, this guanine nucleotide had no effect on cell replicatio
n during this period. Thus Molt 4 cells exposed to c-di-GMP enter the
S phase uncoordinated with their overall replication rate.