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 AbstractOligomerization of yeast alpha-factor receptor detected by fluorescent energy transfer between ligands    Next AbstractPrenatal exposure to a low dose of BPS causes sex-dependent alterations to vascular endothelial function in adult offspring »

Mol Cell Biol


Title:Physical monitoring of mating type switching in Saccharomyces cerevisiae
Author(s):Connolly B; White CI; Haber JE;
Address:"Department of Biology, Brandeis University, Waltham, Massachusetts 02254"
Journal Title:Mol Cell Biol
Year:1988
Volume:8
Issue:6
Page Number:2342 - 2349
DOI: 10.1128/mcb.8.6.2342-2349.1988
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"The kinetics of mating type switching in Saccharomyces cerevisiae can be followed at the DNA level by using a galactose-inducible HO (GAL-HO) gene to initiate the event in synchronously growing cells. From the time that HO endonuclease cleaves MAT a until the detection of MAT alpha DNA took 60 min. When unbudded G1-phase cells were induced, switched to the opposite mating type in 'pairs.' In the presence of the DNA synthesis inhibitor hydroxyurea, HO-induced cleavage occurred but cells failed to complete switching. In these blocked cells, the HO-cut ends of MATa remained stable for at least 3 h. Upon removal of hydroxyurea, the cells completed the switch in approximately 1 h. The same kinetics of MAT switching were also seen in asynchronous cultures and when synchronously growing cells were induced at different times of the cell cycle. Thus, the only restriction that confined normal homothallic switching to the G1 phase of the cell cycle was the expression of HO endonuclease. Further evidence that galactose-induced cells can switch in the G2 phase of the cell cycle was the observation that these cells did not always switch in pairs. This suggests that two chromatids, both cleaved with HO endonuclease, can interact independently with the donors HML alpha and HMRa"
Keywords:"DNA/metabolism DNA Restriction Enzymes/metabolism Electrophoresis, Agar Gel Enzyme Induction Galactose/pharmacology *Genes, Fungal *Genes, Mating Type, Fungal Kinetics Mating Factor Peptides/*pharmacology Promoter Regions, Genetic Saccharomyces cerevisiae;"
Notes:"MedlineConnolly, B White, C I Haber, J E eng GM20056/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 1988/06/01 Mol Cell Biol. 1988 Jun; 8(6):2342-9. doi: 10.1128/mcb.8.6.2342-2349.1988"

 
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 28-12-2024