Me. Wilson et al., THE EFFECT OF ONGOING PROTEIN-SYNTHESIS ON THE STEADY-STATE LEVELS OFGP63 RNAS IN LEISHMANIA-CHAGASI, The Journal of biological chemistry, 268(21), 1993, pp. 15731-15736
G63, the major surface glycoprotein of Leishmania chagasi promastigote
s, increases 11-fold in amount as promastigotes grow from logarithmic
to stationary phase. Transcripts from three different classes of gp63
genes are differentially expressed during this development (Ramamoorth
y, R., Donelson, J. E., Paetz, K. E., Maybodi, M., Roberts, S. P., and
Wilson, M. E. (1992) J. Biol. Chem. 267, 1888-1895). We studied the e
ffect of protein synthesis inhibitors on gp63 mRNAs. The steady state
level of log class gp63 RNA, expressed primarily in logarithmic phase
promastigotes, increased 16.5-fold after incubation in cycloheximide.
A similar increase in log gp63 RNAs was caused by inhibitors that bloc
k different steps in translation. In contrast, the levels of stationar
y class gp63 RNA, expressed in stationary phase parasites, and constit
utive class gp63 RNA, expressed throughout promastigote growth, increa
sed only 2.3- and 1.5-fold, respectively. The latter was not statistic
ally significant. Nuclear run-on assays showed that the cycloheximide
effect was not due to an increased rate of transcription. However, the
t1/2 Of log RNAs was prolonged 6.5-fold after incubation in cyclohexi
mide, in contrast to a 1.7-fold increase in the t1/2 of ATPase RNA, su
ggesting that cycloheximide specifically stabilizes log gp63 mRNAs. Th
us, a highly labile negative regulatory protein, such as an RNase, may
specifically target log gp63 RNAs for degradation.