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 AbstractSystemic biomarkers of exposure associated with ENDS use: a scoping review    Next AbstractOscillatory phosphorylation of yeast Fus3 MAP kinase controls periodic gene expression and morphogenesis »

RNA


Title:Translation-independent inhibition of mRNA deadenylation during stress in Saccharomyces cerevisiae
Author(s):Hilgers V; Teixeira D; Parker R;
Address:"Department of Molecular and Cellular Biology and Howard Hughes Medical Institute, University of Arizona, Tucson, Arizona 85721, USA"
Journal Title:RNA
Year:2006
Volume:20060829
Issue:10
Page Number:1835 - 1845
DOI: 10.1261/rna.241006
ISSN/ISBN:1355-8382 (Print) 1469-9001 (Electronic) 1355-8382 (Linking)
Abstract:"Post-transcriptional control mechanisms play an important role in regulating gene expression during cellular responses to stress. For example, many stresses inhibit translation, and at least some stresses inhibit mRNA turnover in yeast and mammalian cells. We show that hyperosmolarity, heat shock, and glucose deprivation stabilize multiple mRNAs in yeast, primarily through inhibition of deadenylation. Although these stresses inhibit translation and promote the movement of mRNAs into P-bodies, we also observed inhibition of deadenylation in cycloheximide-treated cells as well as in a mutant strain where translation initiation is impaired. This argues that inhibition of poly(A)-shortening is independent of the translational state of the mRNAs and can occur when mRNAs are localized in polysomes or are not engaged in translation. Analysis of pan2Delta or ccr4Delta strains indicates that stress inhibits the function of both the Ccr4p/Pop2p/Notp and the Pan2p/Pan3p deadenylases. We suggest that under stress, simultaneous repression of translation and deadenylation allows cells to selectively translate mRNAs specific to the stress response, while retaining the majority of the cytoplasmic pool of mRNAs for later reuse and recovery from stress. Moreover, because various cellular stresses also inhibit deadenylation in mammalian cells, this mechanism is likely to be a conserved aspect of the stress response"
Keywords:"Kinetics Lipoproteins/genetics/metabolism Pheromones Protein Biosynthesis RNA Processing, Post-Transcriptional RNA Stability RNA, Fungal/genetics/*metabolism RNA, Messenger/genetics/*metabolism Ribonucleases/antagonists & inhibitors/metabolism Saccharomyc;"
Notes:"MedlineHilgers, Valerie Teixeira, Daniela Parker, Roy eng R01 GM045443/GM/NIGMS NIH HHS/ R37 GM045443/GM/NIGMS NIH HHS/ GM45443/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2006/08/31 RNA. 2006 Oct; 12(10):1835-45. doi: 10.1261/rna.241006. Epub 2006 Aug 29"

 
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 26-11-2024