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 AbstractSystemic induction of volatile release in cotton: how specific is the signal to herbivory?    Next AbstractOrganic Chemical Characterization and Mass Balance of a Hydraulically Fractured Well: From Fracturing Fluid to Produced Water over 405 Days »

Cold Spring Harb Protoc


Title:Synchronization and Arrest of the Budding Yeast Cell Cycle Using Chemical and Genetic Methods
Author(s):Rosebrock AP;
Address:"Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada"
Journal Title:Cold Spring Harb Protoc
Year:2017
Volume:20170103
Issue:1
Page Number: -
DOI: 10.1101/pdb.prot088724
ISSN/ISBN:1559-6095 (Electronic) 1559-6095 (Linking)
Abstract:"The cell cycle of budding yeast can be arrested at specific positions by different genetic and chemical methods. These arrests enable study of cell cycle phase-specific phenotypes that would be missed during examination of asynchronous cultures. Some methods for arrest are reversible, with kinetics that enable release of cells back into a synchronous cycling state. Benefits of chemical and genetic methods include scalability across a large range of culture sizes from a few milliliters to many liters, ease of execution, the absence of specific equipment requirements, and synchronization and release of the entire culture. Of note, cell growth and division are decoupled during arrest and block-release experiments. Cells will continue transcription, translation, and accumulation of protein while arrested. If allowed to reenter the cell cycle, cells will do so as a population of mixed, larger-than-normal cells. Despite this important caveat, many aspects of budding yeast physiology are accessible using these simple chemical and genetic tools. Described here are methods for the block and release of cells in G(1) phase and at the M/G(1) transition using alpha-factor mating pheromone and the temperature-sensitive cdc15-2 allele, respectively, in addition to methods for arresting the cell cycle in early S phase and at G(2)/M by using hydroxyurea and nocodazole, respectively"
Keywords:"Cell Cycle Checkpoints/*drug effects/*radiation effects Cell Cycle Proteins/genetics Cell Division/*drug effects/*radiation effects Genetics, Microbial/*methods Hot Temperature Mating Factor/metabolism Microbiological Techniques/*methods Mutant Proteins/m;"
Notes:"MedlineRosebrock, Adam P eng 2017/01/05 Cold Spring Harb Protoc. 2017 Jan 3; 2017(1). doi: 10.1101/pdb.prot088724"

 
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 29-12-2024