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 Abstract"Aroma Profile Development in Beer Fermented with Azacca, Idaho-7, and Sultana Hops"    Next AbstractInduced defense in Nicotiana attenuata (Solanaceae) fruit and flowers »

Mol Cell Biol


Title:Identification and regulation of a gene required for cell fusion during mating of the yeast Saccharomyces cerevisiae
Author(s):McCaffrey G; Clay FJ; Kelsay K; Sprague GF;
Address:"Department of Biology, University of Oregon, Eugene 97403"
Journal Title:Mol Cell Biol
Year:1987
Volume:7
Issue:8
Page Number:2680 - 2690
DOI: 10.1128/mcb.7.8.2680-2690.1987
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"We have devised a screen for genes from the yeast Saccharomyces cerevisiae whose expression is affected by cell type or by the mating pheromones. From this screen we identified a gene, FUS1, whose pattern of expression revealed interesting regulatory strategies and whose product was required for efficient cell fusion during mating. Transcription of FUS1 occurred only in a and alpha cells, not in a/alpha cells, where it was repressed by a1 X alpha 2, a regulatory activity present uniquely in a/alpha cells. Transcription of FUS1 showed an absolute requirement for the products of five STE genes, STE4, STE5, STE7, STE11, and STE12. Since the activators STE4, STE5, and STE12 are themselves repressed by a1 X alpha 2, the failure to express FUS1 in a/alpha cells is probably the result of a cascade of regulatory activities; repression of the activators by a1 X alpha 2 in turn precludes transcription of FUS1. In addition to regulation of FUS1 by cell type, transcription from the locus increased 10-fold or more when a or alpha cells were exposed to the opposing mating pheromone. To investigate the function of the Fus1 protein, we created fus1 null mutants. In fus1 X fus1 matings, the cells of a mating pair adhered tightly and appeared to form zygotes. However, the zygotes were abnormal. Within the conjugation bridge the contained a partition that prevented nuclear fusion and mixing of organelles. The predicted sequence of the Fus1 protein (deduced from the FUS1 DNA sequence) and subcellular fractionation studies with Fus1-beta-galactosidase hybrid proteins suggest that Fus1 is a membrane or secreted protein. Thus, Fus1 may be located at a position within the cell where it is poised to catalyze cell wall or plasma membrane fusion"
Keywords:"Amino Acid Sequence Base Sequence Crosses, Genetic *Genes *Genes, Fungal *Genes, Regulator Genotype Mating Factor Peptides/*genetics Pheromones/genetics Saccharomyces cerevisiae/*genetics/physiology;"
Notes:"MedlineMcCaffrey, G Clay, F J Kelsay, K Sprague, G F Jr eng GM-07413/GM/NIGMS NIH HHS/ GM-30027/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 1987/08/01 Mol Cell Biol. 1987 Aug; 7(8):2680-90. doi: 10.1128/mcb.7.8.2680-2690.1987"

 
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