CELLULAR-PARAMETERS OF THE SHOOT APICAL MERISTEM IN ARABIDOPSIS

Citation
P. Laufs et al., CELLULAR-PARAMETERS OF THE SHOOT APICAL MERISTEM IN ARABIDOPSIS, The Plant cell, 10(8), 1998, pp. 1375-1389
Citations number
34
Categorie Soggetti
Plant Sciences",Biology,"Cell Biology
Journal title
ISSN journal
10404651
Volume
10
Issue
8
Year of publication
1998
Pages
1375 - 1389
Database
ISI
SICI code
1040-4651(1998)10:8<1375:COTSAM>2.0.ZU;2-B
Abstract
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.