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 AbstractDispensers for pheromonal pest control    Next Abstract"Flower volatiles, crop varieties and bee responses" »

FEMS Yeast Res


Title:Mating-type locus control of killer toxins from Kluyveromyces lactis and Pichia acaciae
Author(s):Klassen R; Jablonowski D; Stark MJ; Schaffrath R; Meinhardt F;
Address:"Institut fur Molekulare Mikrobiologie und Biotechnologie, Westfalische Wilhelms-Universitat Munster, Munster, Germany"
Journal Title:FEMS Yeast Res
Year:2006
Volume:6
Issue:3
Page Number:404 - 413
DOI: 10.1111/j.1567-1364.2005.00006.x
ISSN/ISBN:1567-1356 (Print) 1567-1356 (Linking)
Abstract:"Killer-toxin complexes produced by Kluyveromyces lactis and Pichia acaciae inhibit cell proliferation of Saccharomyces cerevisiae. Analysis of their actions in haploid MATalpha cells revealed that introduction of the opposite mating-type locus (MATa) significantly suppressed antizymosis. Together with resistance expressed by MATa/MATalpha diploids, the reciprocal action of MATa or MATalpha in haploids of opposite mating types suggests that these killer toxins may be subject to MAT locus control. Congruently, derepressing the silent mating-type loci, HMR and HML, by removing individual components of the histone deacetylase complex Sir1-4, either by transposon-tagging or by chemically inactivating the histone deacetylase catalytic subunit Sir2, yields toxin resistance. Consistent with MAT control of toxin action, killer-toxin-insensitive S. cerevisiae mutants (kti) become mating-compromised despite resisting the toxins' cell-cycle effects. Mating inhibition largely depends on the time point of toxin application to the mating mixtures and is less pronounced in Elongator mutants, whose resistance to the toxins' cell-cycle effects is the result of toxin-target process deficiencies. In striking contrast, non-Elongator mutants defective in early-response events such as toxin import/activation hardly recover from toxin-induced mating inhibition. This study reveals a novel effect of yeast killer toxins on mating and sexual reproduction that is independent of their impact on cellular proliferation and cell-cycle progression"
Keywords:"*Genes, Mating Type, Fungal Heterozygote Histone Deacetylase Inhibitors Histone Deacetylases/genetics/physiology Killer Factors, Yeast Mating Factor Mutagenesis, Insertional Mutation Mycotoxins/*toxicity Peptides/genetics/physiology Saccharomyces cerevisi;"
Notes:"MedlineKlassen, Roland Jablonowski, Daniel Stark, Michael J R Schaffrath, Raffael Meinhardt, Friedhelm eng Research Support, Non-U.S. Gov't England 2006/04/25 FEMS Yeast Res. 2006 May; 6(3):404-13. doi: 10.1111/j.1567-1364.2005.00006.x"

 
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 13-11-2024