First published online March 7, 2002; 10.1104/pp.010896
Plant Physiol, April 2002, Vol. 128, pp. 1470-1479
Regulation by Polyamines of Ornithine Decarboxylase Activity and
Cell Division in the Unicellular Green Alga Chlamydomonas
reinhardtii1
Christine
Theiss,
Peter
Bohley, and
Jürgen
Voigt*
Physiologisch-Chemisches Institut, Universität
Tübingen, Hoppe-Seyler-Stra e 4, D-72076 Tübingen,
Germany
Polyamines are required for cell growth and cell division in
eukaryotic and prokaryotic organisms. In the unicellular green alga
Chlamydomonas reinhardtii, biosynthesis of the commonly
occurring polyamines (putrescine, spermidine, and spermine) is
dependent on the activity of ornithine decarboxylase (ODC, EC 4.1.1.17) catalyzing the formation of putrescine, which is the precursor of the
other two polyamines. In synchronized C. reinhardtii
cultures, transition to the cell division phase was preceded by a
4-fold increase in ODC activity and a 10- and a 20-fold increase,
respectively, in the putrescine and spermidine levels. Spermine,
however, could not be detected in C. reinhardtii cells.
Exogenous polyamines caused a decrease in ODC activity. Addition of
spermine, but not of spermidine or putrescine, abolished the transition
to the cell division phase when applied 7 to 8 h after beginning
of the light (growth) phase. Most of the cells had already doubled
their cell mass after this growth period. The spermine-induced cell
cycle arrest could be overcome by subsequent addition of spermidine or
putrescine. The conclusion that spermine affects cell division via a
decreased spermidine level was corroborated by the findings that
spermine caused a decrease in the putrescine and spermidine levels and
that cell divisions also could be prevented by inhibitors of
S-adenosyl-methionine decarboxylase and spermidine
synthase, respectively, added 8 h after beginning of the growth
period. Because protein synthesis was not decreased by addition of
spermine under our experimental conditions, we conclude that spermidine affects the transition to the cell division phase directly rather than
via protein biosynthesis.
1
This work was supported by the Deutsche
Forschungsgemeinschaft (grant no. Vo 327/9).
*
Corresponding author; e-mail juergen.voigt{at}uni-tuebingen.de; fax
49-7071-295009.
© 2002 American Society of Plant Physiologists
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