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 AbstractChemistry of odor stimuli    Next AbstractFunctional characterization of the Bombyx mori fatty acid transport protein (BmFATP) within the silkmoth pheromone gland »

J Biol Chem


Title:"Isolation and characterization of a humoral factor that stimulates transcription of the acyl-CoA-binding protein in the pheromone gland of the silkmoth, Bombyx mori"
Author(s):Ohnishi A; Koshino H; Takahashi S; Esumi Y; Matsumoto S;
Address:"RIKEN (The Institute of Physical and Chemical Research), Hirosawa 2-1, Wako, Saitama 351-0198, Japan"
Journal Title:J Biol Chem
Year:2005
Volume:20041206
Issue:6
Page Number:4111 - 4116
DOI: 10.1074/jbc.M413429200
ISSN/ISBN:0021-9258 (Print) 0021-9258 (Linking)
Abstract:"Acyl-CoA binding protein (ACBP) is a highly conserved 10-kDa intracellular lipid-binding protein that binds straight-chain (C14-C22) acyl-CoA esters with high affinity and is expressed in a wide variety of species ranging from yeast to mammals. Functionally, ACBP can act as an acyl-CoA carrier or as an acyl-CoA pool maker within the cell. Much work on the biochemical properties regarding the ACBP has been performed using various vertebrate and plant tissues, as well as different types of cells in culture, the regulatory mechanisms underlying ACBP gene expression have remained poorly understood. By exploiting the unique sex pheromone production system in the moth pheromone gland (PG), we report that transcription of a specific ACBP termed pheromone gland ACBP is triggered by a hemolymph-based humoral factor. Following purification and structure elucidation by means of high resolution electrospray ionization mass spectrometry and NMR analyses, in conjunction with stereochemical analyses using acid hydrolysates, the humoral factor was identified to be beta-D-glucosyl-O-L-tyrosine. Examination of the hemolymph titers during development revealed that the amount of beta-D-glucosyl-O-L-tyrosine dramatically rose prior to eclosion and reached a maximum of 5 mg/ml (about 1 mg/pupa) on the day preceding eclosion, which was consistent with the effective dose of beta-D-glucosyl-O-L-tyrosine in stimulating pheromone gland ACBP transcription in vivo. Furthermore, in vitro assays using trimmed PG indicated that beta-D-glucosyl-O-L-tyrosine acts directly on the PG. These results provide the first evidence that transcription of some ACBPs can be triggered by specific humoral factors"
Keywords:"Acyl Coenzyme A/metabolism Animals Biological Assay Bombyx/*metabolism Diazepam Binding Inhibitor/chemistry Female Hemolymph/metabolism Hydrolysis Magnetic Resonance Spectroscopy Mass Spectrometry Models, Chemical Pheromones/*metabolism Reverse Transcript;"
Notes:"MedlineOhnishi, Atsushi Koshino, Hiroyuki Takahashi, Shunya Esumi, Yasuaki Matsumoto, Shogo eng Research Support, Non-U.S. Gov't 2004/12/14 J Biol Chem. 2005 Feb 11; 280(6):4111-6. doi: 10.1074/jbc.M413429200. Epub 2004 Dec 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 25-11-2024