CELL ARREST IN Gl AND G2 OF THE MITOTIC CYCLE OF VICIA FABA ROOT MERISTEMS

1973 ◽  
Vol 60 (9) ◽  
pp. 889-895 ◽  
Author(s):  
J. Van't Hof ◽  
D. P. Hoppin ◽  
S. Yagi
1961 ◽  
Vol 9 (2) ◽  
pp. 445-462 ◽  
Author(s):  
John Woodard ◽  
Ellen Rasch ◽  
Hewson Swift

In order to investigate some of the cytochemical processes involved in interphase growth and culminating in cell division, a combined autoradiographic and microphotometric study of nucleic acids and proteins was undertaken on statistically seriated cells of Vicia faba root meristems. Adenine-8-C14 and uridine-H3 were used as ribonucleic acid (RNA) precursors, thymidine-H3 as a deoxyribonucleic acid (DNA) precursor, and phenylalanine-3-C14 as a protein precursor. Stains used in microphotometry were Feulgen (DNA), azure B (RNA), pH 2.0 fast green (total protein), and pH 8.1 fast green (histone). The autoradiographic data (representing rate of incorporation per organelle) and the microphotometric data (representing changes in amounts of the various components) indicate that the mitotic cycle may be divided into several metabolic phases, three predominantly anabolic (net increase), and a fourth phase predominantly catabolic (net decrease). The anabolic periods are: 1. Telophase to post-telophase during which there are high rates of accumulation of cytoplasmic and nucleolar RNA and nucleolar and chromosomal total protein. 2. Post-telophase to preprophase characterized by histone synthesis and a diphasic synthesis of DNA with the peak of synthesis at mid-interphase and a minor peak just preceding prophase. The minor peak is coincident with a relatively localized DNA synthesis in several chromosomal regions. This period is also characterized by minimal accumulations of cytoplasmic RNA and chromosomal and nucleolar total protein and RNA. 3. Preprophase to prophase in which there are again high rates of accumulation of cytoplasmic RNA, and nucleolar and chromosomal total protein and RNA. The catabolic phase is: 4. The mitotic division during which there are marked losses of cytoplasmic RNA and chromosomal and nucleolar total protein and RNA.


1969 ◽  
Vol 17 (4) ◽  
pp. 266-272 ◽  
Author(s):  
DONALD P. FOX

Hydrolysis of Vicia faba primary root meristems in 5 NHC1 at 20°C, followed by reaction with the Feulgen reagent, was investigated using microdensitometry. Some differences in response were observed with prophase nuclei fixed in different solutions, but in general this type of hydrolysis leads to a plateau for stainability. After plateau hydrolysis most dye binding is completed within 15 min. For 3:1 alcohol-acetic fixatives, fixation times between 1 day and 13 weeks do not affect plateau stainability but shorter (½ hr) and longer (21 weeks) times give slightly lower values for dye content. Alcohol-acetic fixatives for short periods of time give the least variable results. A comparison of 5 N HCl hydrolysis at 20°C and 30°C shows that at the higher temperature the plateau is brief but not different in dye binding. However, the peak values for 1 N HCl hydrolysis at 60°C are significantly lower by 20%.


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