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 Abstract"Cloning and characterization of the pheromone biosynthesis activating neuropeptide receptor from the silkmoth, Bombyx mori. Significance of the carboxyl terminus in receptor internalization"    Next AbstractBombyx mori homologs of STIM1 and Orai1 are essential components of the signal transduction cascade that regulates sex pheromone production »

J Insect Physiol


Title:The Bombyx mori sex pheromone biosynthetic pathway is not mediated by cAMP
Author(s):Hull JJ; Kajigaya R; Imai K; Matsumoto S;
Address:"Molecular Entomology Laboratory, RIKEN, Hirosawa 2-1, Wako, Saitama 351-0198, Japan. joeh@postman.riken.go.jp"
Journal Title:J Insect Physiol
Year:2007
Volume:20070306
Issue:8
Page Number:782 - 793
DOI: 10.1016/j.jinsphys.2007.02.013
ISSN/ISBN:0022-1910 (Print) 0022-1910 (Linking)
Abstract:"In most moths, sex pheromone production is regulated by pheromone biosynthesis-activating neuropeptide (PBAN). How the extracellular PBAN signal is turned into a biological response has been the focus of numerous studies. In the classical scheme of signal transduction, activated G proteins relay the extracellular signal to downstream effector molecules such as calcium channels and adenylyl cyclase. The role of calcium in PBAN signaling has been clearly demonstrated, but the possible involvement of cAMP is not as straightforward. While cAMP has been shown to be necessary for PBAN signaling in most heliothine species, there has been no definitive demonstration of its role in Bombyx mori. To address this question, we used degenerate RT-PCR to clone two Gs subunits, designated P50Gs1 and P50Gs2, from B. mori pheromone gland (PG) cDNAs. The two Gs proteins were expressed in all tissues examined and were not up-regulated in accordance with adult eclosion. Even though two bands corresponding to the approximate molecular weights of P50Gs1 and P50Gs2 were detected in PG homogenates, the Gs antagonist, NF449, had no effect on sex pheromone production. Furthermore, no changes in the intracellular cAMP levels were detected following PBAN stimulation"
Keywords:"Amino Acid Sequence Animals Base Sequence Bombyx/*metabolism Cyclic AMP/*metabolism GTP-Binding Protein alpha Subunits, Gs/*metabolism Gene Expression Molecular Sequence Data Neuropeptides/*metabolism Polymerase Chain Reaction Sequence Analysis, Protein S;"
Notes:"MedlineHull, J Joe Kajigaya, Ryosuke Imai, Kiyohiro Matsumoto, Shogo eng Research Support, Non-U.S. Gov't England 2007/04/24 J Insect Physiol. 2007 Aug; 53(8):782-93. doi: 10.1016/j.jinsphys.2007.02.013. Epub 2007 Mar 6"

 
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