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"Risk assessments of emerging contaminants in various waters and changes of microbial diversity in sediments from Yangtze River chemical contiguous zone, Eastern China"    Next AbstractReceptor for detection of a Type II sex pheromone in the winter moth Operophtera brumata »

J Insect Physiol


Title:"Sequencing and characterization of six cDNAs putatively encoding three pairs of pheromone receptors in two sibling species, Helicoverpa armigera and Helicoverpa assulta"
Author(s):Zhang DD; Zhu KY; Wang CZ;
Address:"State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, 1 Beichen West Road, Chaoyang District, Beijing 100101, China"
Journal Title:J Insect Physiol
Year:2010
Volume:20091214
Issue:6
Page Number:586 - 593
DOI: 10.1016/j.jinsphys.2009.12.002
ISSN/ISBN:1879-1611 (Electronic) 0022-1910 (Linking)
Abstract:"Pheromone receptors (PRs) on male antennae mediate specific and sensitive detection of sex pheromone components in lepidopterans. In this study, we identified and sequenced six putative cDNAs encoding PRs from sibling species, namely HarmOR1, HarmOR2 and HarmOR3 in Helicoverpa armigera and HassOR1, HassOR2 and HassOR3 in Helicoverpa assulta, which appeared to be orthologs of Heliothis virescens putative PR genes HvOR13, HvOR11 and HvOR16, respectively. Expression patterns of the six PR genes were evaluated by quantitative real-time PCR (qRT-PCR). All the putative PR genes exhibited male-biased expression patterns in adult antennae except for HarmOR2 and HassOR2 that showed similar expression levels in male and female antennae. Expression level of HarmOR1 was significantly higher than those of HarmOR2 and HarmOR3 in male antennae of H. armigera, but the three corresponding PR genes in male antennae of H. assulta showed similar expression levels. This implies the role of the PR encoded by HarmOR1 for interacting with Z11-16:Ald. The level of HarmOR1 transcript was significantly higher than that of HassOR1. These results were consistent with the ratio of Z11-16:Ald in their sex pheromone blends and the abundance of sensilla tuned to Z11-16:Ald on antennae of male adults of the two species"
Keywords:"Animals DNA, Complementary/*genetics Female Gene Expression Regulation/genetics/physiology Genes, Insect/genetics Male Molecular Sequence Data Moths/*genetics/physiology Phylogeny Receptors, Pheromone/*genetics Reverse Transcriptase Polymerase Chain React;"
Notes:"MedlineZhang, Dan-Dan Zhu, Kun Yan Wang, Chen-Zhu eng Research Support, Non-U.S. Gov't England 2009/12/08 J Insect Physiol. 2010 Jun; 56(6):586-93. doi: 10.1016/j.jinsphys.2009.12.002. Epub 2009 Dec 14"

 
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