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 AbstractReal-time monitoring of herbivore induced volatile emissions in the field    Next AbstractSource reconciliation of atmospheric gas-phase and particle-phase pollutants during a severe photochemical smog episode »

Genes Cells


Title:Sequence elements that contribute to the degradation of yeast G alpha
Author(s):Schauber C; Chen L; Tongaonkar P; Vega I; Madura K;
Address:"Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854, USA"
Journal Title:Genes Cells
Year:1998
Volume:3
Issue:5
Page Number:307 - 319
DOI: 10.1046/j.1365-2443.1998.00192.x
ISSN/ISBN:1356-9597 (Print) 1356-9597 (Linking)
Abstract:"BACKGROUND: Gpa1 is the alpha subunit of the yeast G-protein that regulates signal transduction during mating. The stability of Galpha/Gpa1 is influenced by the ubiquitin-dependent N-end rule pathway, suggesting that the regulation of G alpha levels may be important for effective mating response and recovery. RESULTS: The G alpha sequences that confer sensitivity to degradation by the N-end rule pathway were identified. The insertion of this degradation signal (G1-Deg) into the ordinarily stable Gpa2 protein conferred proteolytic targeting. We examined G alpha degradation under different conditions and found that it was efficiently degraded in haploid and diploid cells, but was stable if it was synthesized prior to expression of the N-end rule pathway. Interestingly, a specific mutation in G alpha that is believed to promote the GTP-bound form (N388K) caused accelerated degradation. CONCLUSION: A region encompassing a putative effector-binding domain (G1-Deg) is required for G alpha degradation via the N-end rule pathway. Our studies have shown that G alpha is susceptible to proteolysis soon after synthesis. These results are in agreement with the idea that G alpha is more unstable in the GTP-bound form, which is the predominant state of monomeric/free G alpha soon after synthesis. It is likely that the signal transduced by Gbetagamma can be regulated by adjusting the levels of G alpha through proteolysis"
Keywords:"Amino Acid Sequence Diploidy Enzyme Stability Fungal Proteins/metabolism *GTP-Binding Protein alpha Subunits GTP-Binding Protein alpha Subunits, Gq-G11 GTP-Binding Proteins/chemistry/genetics/*metabolism *GTPase-Activating Proteins Haploidy *Heterotrimeri;"
Notes:"MedlineSchauber, C Chen, L Tongaonkar, P Vega, I Madura, K eng GM52058/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, P.H.S. England 1998/07/31 Genes Cells. 1998 May; 3(5):307-19. doi: 10.1046/j.1365-2443.1998.00192.x"

 
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 19-12-2024