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 AbstractSex pheromones from male forewings of the Common Grass Yellow Eurema mandarina    Next AbstractUltraweak photon emission from herbivory-injured maize plants »

Exp Cell Res


Title:Subcellular localization and oligomeric structure of the yeast putative stretch-activated Ca2+ channel component Mid1
Author(s):Yoshimura H; Tada T; Iida H;
Address:"Department of Biology, Tokyo Gakugei University, 4-1-1 Nukui kita-machi, Koganei-shi, Tokyo 184-8501, Japan"
Journal Title:Exp Cell Res
Year:2004
Volume:293
Issue:2
Page Number:185 - 195
DOI: 10.1016/j.yexcr.2003.09.020
ISSN/ISBN:0014-4827 (Print) 0014-4827 (Linking)
Abstract:"The yeast Mid1 protein with an apparent molecular mass of 100 kDa is required for Ca2+ influx stimulated by the mating pheromone and by a capacitative calcium entrylike mechanism acting in response to Ca2+ depletion from the endoplasmic reticulum (ER) and functions as a stretch-activated Ca2+ -permeable channel when expressed in mammalian cells. Our previous work with protease protection experiments has indicated that Mid1 is present in the plasma membrane. In this study, we examined a possible intracellular localization of this protein by indirect fluorescence microscopy and found that Mid1 is present in the ER membrane as well as the plasma membrane. Intracellular fluorescence images for Mid1 were the same as those for the ER marker protein Sec71 but quite different from those of the Golgi protein Ypt1. The results were confirmed by membrane fractionation using Angiografin density gradient analysis. We also investigated the oligomeric structures and protein levels of Mid1 and found that Mid1 forms a 200-kDa oligomer by disulfide bonding. The protein level and modification of Mid1 in the plasma membrane and the ER membrane were unchanged by the mating pheromone. These findings provide new insight into the function of Mid1 in relation to localization, modification, and activation mechanisms"
Keywords:"Calcium Channels/*metabolism Calcium Signaling/*physiology Cell Membrane/metabolism Cells, Cultured Disulfides/metabolism Endoplasmic Reticulum/*metabolism Intracellular Membranes/metabolism Membrane Glycoproteins/*metabolism Pheromones/metabolism/pharmac;"
Notes:"MedlineYoshimura, Hitoshi Tada, Tomoko Iida, Hidetoshi eng Research Support, Non-U.S. Gov't 2004/01/20 Exp Cell Res. 2004 Feb 15; 293(2):185-95. doi: 10.1016/j.yexcr.2003.09.020"

 
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