Journal of Experimental Botany, Vol 49, 1749-1756, Copyright © 1998 by Oxford University Press
L Sundbland, P Geladi, A Dunberg and B Sundberg
The methodology for determination of mitotic index (MI) from apical
meristems of conifers was improved to permit the efficient processing of
large sample numbers. Improvements were made at three different stages of
the method. Firstly, hydrolysis, staining, cytoplasmic bleaching, washing
of samples, and temperature regimes were automated, which reduced the need
for labour and improved the standardization of chemical treatment.
Secondly, the use of vertical and controlled pressure for squashing
improved the quality of the preparations and decreased the fraction of
discarded preparations. Thirdly, an interactive image analysis system for
estimation of MI from preparations was constructed. This system increased
the efficiency of analysis of preparations, but did not eliminate
subjective manual classification of nuclei into cell cycle stages. The
possibility of using fully automated image analysis for estimation of MI
was investigated using a standard image processing sequence and by
multivariate analysis of image analysis parameters. For this, principal
component analysis (PCA) was used to detect cell cycle stage related
clustering of nuclei in score plots. PCA was also used to construct a model
based on interphase nuclei that enabled correct classification of 25 nuclei
from five cell cycle stages as either dividing or non-dividing.Key words:
Mitotic index, image analysis, apical meristem, conifer.
ARTICLES
The use of image analysis and automation for measuring mitotic index in apical conifer meristems
Forestry Research Institute of Sweden, Box 3, S-918 21 Savar, Sweden; Department Organic Chemistry, Umea University, S-901 87 Umea, Sweden; OmniVisor, Box 2722, S-762 94 Rimbo, Sweden; Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, S-901 83 Umea, Sweden; Corresponding author
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