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Increased cell cycle‐dependent staining of plant cells by the antibody MPM‐2 correlates with preprophase band formation
Author(s) -
Young T.,
Hyams J.S.,
Lloyd C.W.
Publication year - 1994
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1046/j.1365-313x.1994.05020279.x
Subject(s) - mitosis , interphase , dapi , biology , microtubule , microbiology and biotechnology , tubulin , spindle apparatus , cell , staining , cell division , biochemistry , genetics
Cytoplasmic microtubules of animal cells catastrophically depolymerize upon entry into mitosis but in higher plants there is a longer transition during which cortical microtubules form an increasingly narrow preprophase band, and the chromatin gradually condenses. Progression towards mitosis in onion root tip cells was analysed using a CCD camera and image processing to quantify fluorescence staining by the monoclonal antibody MPM‐2, which recognizes mitotic phosphoproteins in a range of eukaryotic cells. MPM‐2 fluorescence, which was predominantly nuclear, was categorized relative to the stage of the DNA cycle (using DAPI), and to the microtubule cycle (using anti‐tubulin) in individual cells. Cells with the characteristic interphase cortical microtubule arrays had a bimodal distribution of DAPI fluorescence, indicating that some were in G1 (2C DNA) whilst the double value suggested the others to be in G2 (4C). There was no difference in MPM‐2 fluorescence between 2C and 4C cells possessing the cortical array in which microtubules were evenly distributed. However, in 4C cells possessing a preprophase band MPM‐2 values doubled; this relationship applied not only to tight PPBs but to early, broad PPBs in which the individual microtubules could still be distinguished. Since alkaline phosphatase abolished MPM‐2 reactivity it is concluded that mitotic phosphoproteins do not necessarily begin to accumulate in G2 per se , but during that part of G2 when the preprophase band first becomes recognizable as a distinct entity.