Document Detail


Transcriptional control of behavior: engrailed knock-out changes cockroach escape trajectories.
MedLine Citation:
PMID:  19494140     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The cerci of the cockroach are covered with identified sensory hairs that detect air movements. The sensory neurons that innervate these hairs synapse with giant interneurons in the terminal ganglion that in turn synapse with interneurons and leg motor neurons in thoracic ganglia. This neural circuit mediates the animal's escape behavior. The transcription factor Engrailed (En) is expressed only in the medially born sensory neurons, which suggested that it could work as a positional determinant of sensory neuron identity. Previously, we used double-stranded RNA interference to abolish En expression and found that the axonal arborization and synaptic outputs of an identified En-positive sensory neuron changed so that it came to resemble a nearby En-negative cell, which was itself unaffected. We thus demonstrated directly that En controls synaptic choice, as well as axon projections. Is escape behavior affected as a result of this miswiring? We showed recently that adult cockroaches keep each escape unpredictable by running along one of a set of preferred escape trajectories (ETs) at fixed angles from the direction of the threatening stimulus. The probability of selecting a particular ET is influenced by wind direction. In this present study, we show that early instar juvenile cockroaches also use those same ETs. En knock-out significantly perturbs the animals' perception of posterior wind, altering the choice of ETs to one more appropriate for anterior wind. This is the first time that it has been shown that knock-out of a transcription factor controlling synaptic connectivity can alter the perception of a directional stimulus.
Authors:
David Booth; Bruno Marie; Paolo Domenici; Jonathan M Blagburn; Jonathan P Bacon
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of neuroscience : the official journal of the Society for Neuroscience     Volume:  29     ISSN:  1529-2401     ISO Abbreviation:  J. Neurosci.     Publication Date:  2009 Jun 
Date Detail:
Created Date:  2009-06-04     Completed Date:  2009-06-22     Revised Date:  2013-06-02    
Medline Journal Info:
Nlm Unique ID:  8102140     Medline TA:  J Neurosci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  7181-90     Citation Subset:  IM    
Affiliation:
Sussex Centre for Neuroscience, School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom.
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MeSH Terms
Descriptor/Qualifier:
Age Factors
Animals
Behavior, Animal / drug effects,  physiology
Cockroaches / anatomy & histology,  physiology*
Computer Simulation
Escape Reaction / drug effects,  physiology*
Ganglia, Invertebrate / cytology,  drug effects,  physiology
Homeodomain Proteins / antagonists & inhibitors*,  genetics
Models, Biological
Physical Stimulation
Probability
RNA, Double-Stranded / pharmacology
Sensory Receptor Cells / drug effects
Spatial Behavior / drug effects,  physiology*
Wind
Grant Support
ID/Acronym/Agency:
G12 RR03051/RR/NCRR NIH HHS; SC2 NS065384/NS/NINDS NIH HHS; SC2 NS065384-01/NS/NINDS NIH HHS; SC2 NS065384-02/NS/NINDS NIH HHS; //Biotechnology and Biological Sciences Research Council
Chemical
Reg. No./Substance:
0/Homeodomain Proteins; 0/RNA, Double-Stranded
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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