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Plant Physiol, December 2000, Vol. 124, pp. 1668-1677
Chloroplast Division and Morphology Are Differentially Affected
by Overexpression of FtsZ1 and FtsZ2 Genes
in Arabidopsis1,[w]
Kevin D.
Stokes,2
Rosemary S.
McAndrew,2
Rubi
Figueroa,
Stanislav
Vitha, and
Katherine W.
Osteryoung*
Department of Botany and Plant Pathology, 166 Plant Biology
Building, Michigan State University, East Lansing, Michigan 48824-1312
(K.D.S., R.S.M., S.V., K.W.O.); and Department of Biochemistry, Mail
Stop 200, University of Nevada, Reno, Nevada 89557 (R.F.)
In higher plants, two nuclear gene families, FtsZ1
and FtsZ2, encode homologs of the bacterial protein
FtsZ, a key component of the prokaryotic cell division machinery. We
previously demonstrated that members of both gene families are
essential for plastid division, but are functionally distinct. To
further explore differences between FtsZ1 and FtsZ2 proteins we
investigated the phenotypes of transgenic plants overexpressing
AtFtsZ1-1 or AtFtsZ2-1, Arabidopsis members of the FtsZ1 and FtsZ2 families,
respectively. Increasing the level of AtFtsZ1-1 protein as little as
3-fold inhibited chloroplast division. Plants with the most severe
plastid division defects had 13- to 26-fold increases in AtFtsZ1-1
levels over wild type, and some of these also exhibited a novel
chloroplast morphology. Quantitative immunoblotting revealed a
correlation between the degree of plastid division inhibition and the
extent to which the AtFtsZ1-1 protein level was elevated. In contrast,
expression of an AtFtsZ2-1 sense transgene had no
obvious effect on plastid division or morphology, though AtFtsZ2-1
protein levels were elevated only slightly over wild-type levels. This
may indicate that AtFtsZ2-1 accumulation is more tightly regulated than
that of AtFtsZ1-1. Plants expressing the AtFtsZ2-1
transgene did accumulate a form of the protein smaller than those
detected in wild-type plants. AtFtsZ2-1 levels were unaffected by
increased or decreased accumulation of AtFtsZ1-1 and vice versa,
suggesting that the levels of these two plastid division proteins are
regulated independently. Taken together, our results provide additional
evidence for the functional divergence of the FtsZ1 and
FtsZ2 plant gene families.
1
This work was supported by the U.S. National
Science Foundation (grant no. MCB-9604412) and by the Nevada
Agricultural Experiment Station.
2
These authors contributed equally to this work.
[w]
Indicates Web-only data.
*
Corresponding author; osteryou{at}msu.edu; fax 517-353-1926.
© 2000 American Society of Plant Physiologists
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