Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractRapid steroid influences on visually guided sexual behavior in male goldfish    Next AbstractUsing multiple array sensing and non-invasive data capture as a model for polypharmacy error detection »

J Cell Sci


Title:Rate of cell cycle initiation of yeast cells when cell size is not a rate-determining factor
Author(s):Lord PG; Wheals AE;
Address:
Journal Title:J Cell Sci
Year:1983
Volume:59
Issue:
Page Number:183 - 201
DOI: 10.1242/jcs.59.1.183
ISSN/ISBN:0021-9533 (Print) 0021-9533 (Linking)
Abstract:"The control of cell proliferation under steady-state conditions in the budding yeast, Saccharomyces cerevisiae, is well described by either the tandem or sloppy size control models, both of which suggest that differences in cycle time between individual cells or between parents and daughters is largely due to differences in birth size. These models have been investigated further under conditions in which cell size has not been a rate-determining factor for cell cycle initiation. Two approaches have been used. The first involves the growth of cells in low concentrations of hydroxyurea (HU), which has the effect of prolonging the duration of DNA synthesis. This leads to a lengthening of the budded period, which in turn leads to daughter cells being larger at division than the normal cell cycle initiation size of daughters in steady-state populations. The second approach involves the accumulation of cells at the key control point of the cycle, called start, using the pheromone alpha-factor. Since growth is unaffected, all cells eventually become larger than the volume at which they would normally initiate the cell cycle. The kinetics of proliferation were followed after release from alpha-factor arrest. The results from both approaches were broadly consistent with the predictions of both models. However, abolition of birth-size differences between parents and daughters in the presence of HU did not lead to a complete disappearance of differences in either cycle time or proliferation kinetics. Furthermore, following release from alpha-factor arrest, the rate of cell cycle initiation of parent cells was slower than in steady-state culture and the daughters' cells behaved as if comprising two separate populations. These discrepancies suggest that besides a size difference, there are additional physiological differences between parent and daughter cells"
Keywords:"Animals Cell Cycle Cell Division/drug effects DNA, Fungal/biosynthesis Hydroxyurea/metabolism Kinetics Mating Factor Peptides/pharmacology Pheromones/pharmacology Saccharomyces cerevisiae/*cytology/metabolism;"
Notes:"MedlineLord, P G Wheals, A E eng Research Support, Non-U.S. Gov't England 1983/01/01 J Cell Sci. 1983 Jan; 59:183-201. doi: 10.1242/jcs.59.1.183"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 05-12-2024