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 AbstractHost selection behavior of a thistle-feeding fly: choices and consequences    Next AbstractThe Arabidopsis extracellular UNUSUAL SERINE PROTEASE INHIBITOR functions in resistance to necrotrophic fungi and insect herbivory »

Nucleic Acids Res


Title:Involvement of SRE element of Ty1 transposon in TEC1-dependent transcriptional activation
Author(s):Laloux I; Jacobs E; Dubois E;
Address:"Laboratoire de Microbiologie, Universite Libre de Bruxelles, Belgium"
Journal Title:Nucleic Acids Res
Year:1994
Volume:22
Issue:6
Page Number:999 - 1005
DOI: 10.1093/nar/22.6.999
ISSN/ISBN:0305-1048 (Print) 1362-4962 (Electronic) 0305-1048 (Linking)
Abstract:"Some Ty1 transposable element insertion mutations of Saccharomyces cerevisiae activate transcription of adjacent genes in a cell-type dependent manner. This activation requires at least STE12 and TEC1 gene products. The binding site for the STE12 protein is located in the sterile responsive element (SRE), which is just downstream the 5' LTR of Ty1 and contains one copy of the pheromone response element (PRE). This report defines the sequences in Ty1 required for TEC1-dependent activation using a TDH3::lacZ reporter gene in which the UAS was replaced by different portions of a Ty1 or Ty2 element. The Ty1 SRE seems to be sufficient to ensure the TEC1 and STE12-mediated activation whereas Ty2 SRE can activate the expression of the adjacent genes in the absence of both proteins. Adjacent to the PRE element, there is a region (PAE) with extensive sequence divergence in Ty1 and Ty2 SREs. Swapping experiments between Ty1 and Ty2 sequences show that Ty1 PAE is required for the activation of adjacent gene expression in a TEC1 and STE12-dependent manner. The use of a LexA::TEC1 construct indicates that the chimeric protein has no activation ability suggesting that TEC1 could act in conjunction with another factor"
Keywords:"Base Sequence Binding Sites Cloning, Molecular *DNA Transposable Elements DNA, Fungal/chemistry DNA-Binding Proteins/*pharmacology Enhancer Elements, Genetic Fungal Proteins/pharmacology Gene Transfer Techniques *Genes, Fungal Molecular Sequence Data Muta;"
Notes:"MedlineLaloux, I Jacobs, E Dubois, E eng Research Support, Non-U.S. Gov't England 1994/03/25 Nucleic Acids Res. 1994 Mar 25; 22(6):999-1005. doi: 10.1093/nar/22.6.999"

 
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 16-11-2024