The shoot apical meristem (SAM) is a small group of dividing cells tha
t generate all of the aerial parts of the plant. With the goal of prov
iding a framework for the analysis of Arabidopsis meristems at the cel
lular level, we performed a detailed morphometric study of actively gr
owing inflorescence apices of the Landsberg erecta and Wassilewskija e
cotypes. For this purpose, cell size, spatial distribution of mitotic
cells, and the mitotic index were determined in a series of optical se
ctions made with a confocal laser scanning microscope. The results all
owed us to identify zones within the inflorescence SAM with different
cell proliferation rates. In particular, we were able to define a cent
ral area that was four to six cells wide and had a low mitotic index.
We used this technique to compare the meristem of the wild type with t
he enlarged meristems of two mutants, clavata3-1 (clv3-1) and mgoun2 (
mgo2). One of the proposed functions of the CLV genes is to limit cell
division rates in the center of the meristem. Our data allowed us to
reject this hypothesis, because the mitotic index was reduced in the i
nflorescence meristem of the clv3-1 mutant. We also observed a targe z
one of slowly dividing cells in meristems of clv3-1 seedlings. This to
ne was not detectable in the wild type. These results suggest that the
central area is increased in size in the mutant meristem, which is in
line with the hypothesis that the CLV3 gene is necessary for the tran
sition of cells from the central to the peripheral zone. Genetic and m
icroscopic analyses suggest that mgo2 is impaired in the production of
primordia, and we previously proposed that the increased size of the
mgo2 meristem could be due to an accumulation of cells at the peripher
y. Our morphometric analysis showed that mgo2 meristems, in contrast t
o those of clv3-1, have an enlarged periphery with high cell prolifera
tion rates. This confirms that clv3-1 and mgo2 lead to meristem overgr
owth by affecting different aspects of meristem function.