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 AbstractThe timing of induced resistance and induced susceptibility in the soybean-Mexican bean beetle system    Next AbstractTrapTech R-Octenol Lure Does Not Improve the Capture Rates of Aedes albopictus (Diptera: Culicidae) and Other Container-Inhabiting Species in Biogents Sentinel Traps »

Bio Protoc


Title:Synchronization of Saccharomyces cerevisiae Cells in G1 Phase of the Cell Cycle
Author(s):Unk I; Daraba A;
Address:"The Institute of Genetics, Biological Research Center of The Hungarian Academy of Sciences, Szeged, Hungary"
Journal Title:Bio Protoc
Year:2014
Volume:4
Issue:20
Page Number: -
DOI: 10.21769/BioProtoc.1273
ISSN/ISBN:2331-8325 (Print) 2331-8325 (Electronic) 2331-8325 (Linking)
Abstract:"The baker's yeast, Saccharomyces cerevisiae is a widely used model organism in molecular biology because of the high homology it shares with human cells in many basic cellular processes such as DNA replication, repair, recombination, transcription, and because of the ease its genome can be manipulated. Other advantages of working with yeast are its fast production rate which is comparable to bacteria's, and its cheap maintenance. To examine certain phenomena, for example whether a mutation affects the passage through a cell cycle phase, it can be necessary to work with a yeast culture, in which all the cells are in the same phase of the cell cycle. Yeasts can be arrested and kept in different phases of the cell cycle. Here we describe the method that allows synchronizing and keeping yeast cells in the G1 phase of the cell cycle with the mating pheromone, alpha-factor. Only MATa cells can be synchronized with alpha-factor which is produced by MATalpha cells. It is highly recommended to use a MATa bar1 deletion strain. The BAR1 gene encodes for an extracellular protease that inactivates alpha-factor by cleaving it (MacKay et al., 1988). To counteract the Bar1 protease activity when using BAR1 cells, 100-1,000 times more alpha-factor is needed as compared to bar1 deletion cells (alpha-factor is quite expensive!), and still the synchrony will be transient. In contrast, bar1 deletion cells can be kept in G1 phase with alpha-factor for several hours, and the degree of synchronization is usually higher than using a BAR1 strain. Moreover, bar1 deletion cells can be synchronized even at high cell density, whereas BAR1 cells, due to the activity of the secreted Bar1 protease, only at low cell density"
Keywords:
Notes:"PubMed-not-MEDLINEUnk, Ildiko Daraba, Andreea eng Wellcome Trust/United Kingdom 070247/Wellcome Trust/United Kingdom 2014/10/20 Bio Protoc. 2014 Oct 20; 4(20):e1273. doi: 10.21769/BioProtoc.1273"

 
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 22-11-2024