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 AbstractDisruptive selection maintains variable pheromone blends in the bark beetle Ips pini    Next AbstractCritical review: the health significance of environmental odor pollution »

Mol Cell Biol


Title:Mating-defective ste mutations are suppressed by cell division cycle start mutations in Saccharomyces cerevisiae
Author(s):Shuster JR;
Address:
Journal Title:Mol Cell Biol
Year:1982
Volume:2
Issue:9
Page Number:1052 - 1063
DOI: 10.1128/mcb.2.9.1052-1063.1982
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"Temperature-sensitive mutants which arrest in the G1 phase of the cell cycle have been described for the yeast Saccharomyces cerevisiae. One class of these mutants (carrying cdc28, cdc36, cdc37, or cdc39) forms a shmoo morphology at restrictive temperature, characteristic of mating pheromone-arrested wild-type cells. Therefore, one hypothesis to explain the control of cell division by mating factors states that mating pheromones arrest wild-type cells by inactivating one or more of these CDC gene products. A class of mutants (carrying ste4, ste5, ste7, ste11, or ste12) which is insensitive to mating pheromone and sterile has also been described. One possible function of the STE gene products is the inactivation of the CDC gene products in the presence of a mating pheromone. A model incorporating these two hypotheses predicts that such STE gene products will not be required for mating in strains carrying an appropriate cdc lesion. This prediction was tested by assaying the mating abilities of double mutants for all of the pairwise combinations of cdc and ste mutations. Lesions in either cdc36 or cdc39 suppressed the mating defect due to ste4 and ste5. Allele specificity was observed in the suppression of both ste4 and ste5. The results indicate that the CDC36, CDC39, STE4, and STE5 gene products interact functionally or physically or both in the regulation of cell division mediated by the presence or absence of mating pheromones. The cdc36 and cdc39 mutations did not suppress ste7, ste11, or ste12. Lesions in cdc28 or cdc37 did not suppress any of the ste mutations. Other models of CDC and STE gene action which predicted that some of the cdc and ste mutations would be alleles of the same locus were tested. None of the cdc mutations was allelic to the ste mutations and, therefore, these models were eliminated"
Keywords:"*Cell Division *Conjugation, Genetic Genetic Complementation Test Genetic Linkage Mating Factor Models, Genetic Mutation Peptides/*genetics Phenotype Saccharomyces cerevisiae/*genetics Suppression, Genetic;"
Notes:"MedlineShuster, J R eng GM00182/GM/NIGMS NIH HHS/ GM07735/GM/NIGMS NIH HHS/ GM17709/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. 1982/09/01 Mol Cell Biol. 1982 Sep; 2(9):1052-63. doi: 10.1128/mcb.2.9.1052-1063.1982"

 
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 26-12-2024