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 AbstractCeramide signals for initiation of yeast mating-specific cell cycle arrest    Next AbstractLong-term storage of Pink Lady apples modifies volatile-involved enzyme activities: consequences on production of volatile esters »

Cell Cycle


Title:A link between very long chain fatty acid elongation and mating-specific yeast cell cycle arrest
Author(s):Villasmil ML; Gallo-Ebert C; Liu HY; Francisco J; Nickels JT;
Address:"a Cato Research Ltd. , Durham , NC , USA. b Institute of Metabolic Disorders, Genesis Biotechnology Group , Hamilton , NJ , USA. c RAMNJ , Basking Ridge , NJ , USA"
Journal Title:Cell Cycle
Year:2017
Volume:20170907
Issue:22
Page Number:2192 - 2203
DOI: 10.1080/15384101.2017.1329065
ISSN/ISBN:1551-4005 (Electronic) 1538-4101 (Print) 1551-4005 (Linking)
Abstract:"Ceramides and sphingolipid intermediates are well-established regulators of the cell cycle. In the budding yeast Saccharomyces cerevisae, the complex sphingolipid backbone, ceramide, comprises a long chain sphingoid base, a polar head group, and a very long chain fatty acid (VLCFA). While ceramides and long chain bases have been extensively studied as to their roles in regulating cell cycle arrest under multiple conditions, the roles of VLCFAs are not well understood. Here, we used the yeast elo2 and elo3 mutants, which are unable to elongate fatty acids, as tools to explore if maintaining VLCFA elongation is necessary for cell cycle arrest in response to yeast mating. We found that both elo2 and elo3 cells had severely reduced mating efficiencies and were unable to form polarized shmoo projections that are necessary for cell-cell contact during mating. They also lacked functional MAP kinase signaling activity and were defective in initiating a cell cycle arrest in response to pheromone. Additional data suggests that mislocalization of the Ste5 scaffold in elo2 and elo3 mutants upon mating initiation may be responsible for the inability to initiate a cell cycle arrest. Moreover, the lack of proper Ste5 localization may be caused by the inability of mutant cells to mobilize PIP(2). We suggest that VLCFAs are required for Ste5 localization, which is a necessary event for initiating MAP kinase signaling and cell cycle arrest during yeast mating initiation"
Keywords:Cell Cycle Checkpoints/*physiology Ceramides/metabolism Fatty Acids/*metabolism Saccharomyces cerevisiae/metabolism Saccharomyces cerevisiae Proteins/metabolism Signal Transduction Sphingolipids/metabolism Mapk cell cycle ceramide lipid yeast;
Notes:"MedlineVillasmil, Michelle L Gallo-Ebert, Christina Liu, Hsing-Yin Francisco, Jamie Nickels, Joseph T Jr eng 2017/07/27 Cell Cycle. 2017; 16(22):2192-2203. doi: 10.1080/15384101.2017.1329065. Epub 2017 Sep 7"

 
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