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"Attraction of male European tarnished plant bug, Lygus rugulipennis to components of the female sex pheromone in the field"    Next AbstractEnhanced cell-surface display and secretory production of cellulolytic enzymes with Saccharomyces cerevisiae Sed1 signal peptide »

Mol Cell Biol


Title:Identification of sequence elements that confer cell-type-specific control of MF alpha 1 expression in Saccharomyces cerevisiae
Author(s):Inokuchi K; Nakayama A; Hishinuma F;
Address:"Laboratory of Molecular Genetics, Mitsubishi-Kasei Institute of Life Sciences, Tokyo, Japan"
Journal Title:Mol Cell Biol
Year:1987
Volume:7
Issue:9
Page Number:3185 - 3193
DOI: 10.1128/mcb.7.9.3185-3193.1987
ISSN/ISBN:0270-7306 (Print) 1098-5549 (Electronic) 0270-7306 (Linking)
Abstract:"The MF alpha 1 gene of Saccharomyces cerevisiae, a major structural gene for mating pheromone alpha factor, is an alpha-specific gene whose expression is regulated by the mating-type locus. To study the role of sequences upstream of MF alpha 1 in its expression and regulation, we generated two sets of promoter deletions: upstream deletions and internal deletions. By analyzing these deletions, we have identified a TATA box and two closely related, tandemly arranged upstream activation sites as necessary elements for MF alpha 1 expression. Two upstream activation sites were located ca. 300 and 250 base pairs upstream of the MF alpha 1 transcription start points, which were also determined in this study. Each site contained a homologous 22-base-pair sequence, and both sites were required for maximum transcription level. The distance between the upstream activation sites and the transcription start points could be altered without causing loss of transcription efficiency, and the sites were active in either orientation with respect to the coding region. These elements conferred cell type-specific expression on a heterologous promoter. Analysis with host mating-type locus mutants indicates that these sequences are the sites through which the MAT alpha 1 product exerts its action to activate the MF alpha 1 gene. Homologous sequences with these elements were found in other alpha-specific genes, MF alpha 2 and STE3, and may mediate activation of this set of genes by MAT alpha 1"
Keywords:"Base Sequence Chromosome Deletion Gene Expression Regulation Genes *Genes, Fungal *Genes, Mating Type, Fungal *Genes, Regulator Genetic Engineering Mating Factor Molecular Sequence Data Mutation Peptides/*genetics *Promoter Regions, Genetic RNA, Fungal/ge;"
Notes:"MedlineInokuchi, K Nakayama, A Hishinuma, F eng Research Support, Non-U.S. Gov't 1987/09/01 Mol Cell Biol. 1987 Sep; 7(9):3185-93. doi: 10.1128/mcb.7.9.3185-3193.1987"

 
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 06-11-2024