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 AbstractThe prepared mind of the worm    Next AbstractVacuum Ultraviolet Spectroscopy and Mass Spectrometry: A Tandem Detection Approach for Improved Identification of Gas Chromatography-Eluting Compounds »

J Biol Chem


Title:Overexpression of eIF4E in Saccharomyces cerevisiae causes slow growth and decreased alpha-factor response through alterations in CLN3 expression
Author(s):Anthony C; Zong Q; De Benedetti A;
Address:"Department of Biochemistry and Molecular Biology, Louisiana State University Health Sciences Center, 1501 Kings Highway, Shreveport, LA 71130-3932, USA"
Journal Title:J Biol Chem
Year:2001
Volume:20010730
Issue:43
Page Number:39645 - 39652
DOI: 10.1074/jbc.M101564200
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"The association of G(1) cyclins and Cdc28/cyclin-dependent protein kinase catalyzes the cell cycle entry (Start) in budding yeast. Activation of Start is presumed to be triggered by a post-transcriptional increase in Cln3 during early G(1). Cells arrested by mating pheromone show a loss of cyclin-dependent protein kinase activity caused by transcriptional shutoff of cyclins and/or inhibition by Far1. We report that overexpression of eIF4E (Cdc33), a rate-limiting translation initiation factor, causes an increase in CLN3 mRNA translation, which results in increased expression of CLN2 and in slow growth and decreased alpha-factor response. This phenotype was abrogated in a Deltacln3 or Deltacln2 background. We isolated the transcription factor MBP1 as a multicopy suppressor of the growth and alpha-factor response defects. Furthermore, elevated MBP1, a transcriptional regulator of cyclins, altered the transcriptional start site in CLN3 mRNA, shifting it 45 nucleotides upstream of the normal. This lengthened 5'-untranslated region likely reduces translation efficiency and down-regulates CLN3 protein synthesis, thereby correcting for the excess translation promoted by elevated Cdc33. In addition, the CLN2 mRNA level returned to normal. We propose that regulation of translation initiation by Cdc33 plays a pivotal role in the activation of Start and cell cycle progression in budding yeast"
Keywords:Cell Cycle Cell Cycle Proteins/*metabolism Cyclins/deficiency/genetics/*metabolism Eukaryotic Initiation Factor-4E Fungal Proteins/genetics/*metabolism Gene Deletion Mating Factor Peptide Initiation Factors/*metabolism Peptides/*pharmacology Phenotype Sac;
Notes:"MedlineAnthony, C Zong, Q De Benedetti, A eng CA 69148/CA/NCI NIH HHS/ GM 57912/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. 2001/08/02 J Biol Chem. 2001 Oct 26; 276(43):39645-52. doi: 10.1074/jbc.M101564200. Epub 2001 Jul 30"

 
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 22-11-2024