1998 Volume 23 Issue 5 Pages 379-388
Methylmercury (MeHg) specifically depolymerizes microtubules and inhibits cell proliferation in mouse glioma cells. The effect of microtubule depolymerization by MeHg on tubulin synthesis was studied. Tubulin synthesis analyzed by two-dimensional electrophoresis using [35S] methionine as a tracer was markedly inhibited in mouse glioma cells exposed to 5×10-6M MeHg for 3 hr, which completely depolymerized microtubules. Under this condition, density of the protein bands other than tubulin in autoradiogram remained unchanged on gradient urea-polyacrylamide gels. Furthermore, the decrease in tubulin mRNA level was relevant to that in tubulin synthesis, although action mRNA levels remaind unchanged. In addition, specific transcription rates of β-tubulin genes appeared to be unaffected under the same experimental condition as above. Thus, it is concluded tht the disruption of microtubules by MeHg resulted in the inhibition of the synthesis of tubulin itself through autoregulatory repression in post-transcriptional processes as in the case of colchicine treatment.