Delayed incorporation of H3-thymidine by primordial cells |
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Authors: | Dr. R. D. MacLeod D. Davidson |
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Affiliation: | (1) Biology Department, Case-Western Reserve University, Cleveland, Ohio;(2) Biology Department, University of Missouri at St. Louis, 63121 St. Louis, Missouri, USA |
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Abstract: | ![]() Roots of Vicia faba were treated with H3-thymidine (1 c/ml) for 1 h and incorporation of H3-TdR into nuclei of primordia was studied. Large primordia (>1,500 cells) did not incorporate H3-TdR. Cells of small primordia did not incorporate the labeled precursor immediately but did so after a delay of several hours. The frequency of labeled nuclei became similar to that of lateral meristems only after a delay of 12–14 h. The gradual increase in labeling index also occurs in colchicine treated cells, which do not divide; this shows that the rise in labeling index is not due solely to the division of labeled cells. It has been estimated from H3-TdR and colchicine labeled cells that small primordia have a population of cells in which intermitotic time is about 12 h. The delay in incorporation appears to indicate that pools of H3-TdR can be maintained in small primordia for several hrs and that the precursor is not used until the cells synthesize thymidine kinase.This research has been supported by the U.S.A.E.C. [Grant AT (11-1) 1625-12]. |
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