Literature DB >> 16862440

Anatomy, physiology and pharmacology of Caenorhabditis elegans pharynx: a model to define gene function in a simple neural system.

Christopher J Franks1, Lindy Holden-Dye, Kathryn Bull, Sarah Luedtke, Robert J Walker.   

Abstract

Invertebrate neuroscience has provided a number of very informative model systems that have been extensively utilized in order to define the neurobiological bases of animal behaviours (Sattelle and Buckingham in Invert Neurosci 6:1-3, 2006). Most eminent among these are a number of molluscs, including Aplysia californica, Lymnaea stagnalis and Helix aspersa, crustacean systems such as the crab stomatogastric ganglion and a wide-range of other arthropods. All of these have been elegantly exploited to shed light on the very important phenomenon of the molecular and cellular basis for synaptic regulation that underpins behavioural plasticity. Key to the successful use of these systems has been the ability to study well-defined, relatively simple neuronal circuits that direct and regulate a quantifiable animal behaviour. Here we describe the pharyngeal system of the nematode C. elegans and its utility as a model for defining the genetic basis of behaviour. The circuitry of the nervous system in this animal is uniquely well-defined. Furthermore, the feeding behaviour of the worm is controlled by the activity of the pharynx and this in turn is regulated in a context-dependent manner by a simple nervous system that integrates external signals, e.g. presence or absence of food, and internal signals, e.g. the nutritional status of the animal to direct an appropriate response. The genetics of C. elegans is being effectively exploited to provide novel insight into genes that function to regulate the neuronal network that controls the pharynx. Here we summarise the progress to date and highlight topics for future research. Two main themes emerge. First, although the anatomy of the pharyngeal system is very well-defined, there is a much poorer understanding of its neurochemistry. Second, it is evident that the neurochemistry is remarkably complex for such a simple circuit/behaviour. This suggests that the pharyngeal activity may be subject to exquisitely precise regulation depending on the animal's environment and status. This therefore provides a very tractable genetic model to investigate neural mechanisms for signal integration and synaptic plasticity in a well-defined neuronal network that directs a quantifiable behaviour, feeding.

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Year:  2006        PMID: 16862440     DOI: 10.1007/s10158-006-0023-1

Source DB:  PubMed          Journal:  Invert Neurosci        ISSN: 1354-2516


  86 in total

1.  The pharynx of Caenorhabditis elegans.

Authors:  D G Albertson; J N Thomson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1976-08-10       Impact factor: 6.237

2.  aex-3 encodes a novel regulator of presynaptic activity in C. elegans.

Authors:  K Iwasaki; J Staunton; O Saifee; M Nonet; J H Thomas
Journal:  Neuron       Date:  1997-04       Impact factor: 17.173

Review 3.  The pacemaker activity of interstitial cells of Cajal and gastric electrical activity.

Authors:  P Camborová; P Hubka; I Sulková; I Hulín
Journal:  Physiol Res       Date:  2003       Impact factor: 1.881

4.  Identification of neuropeptide-like protein gene families in Caenorhabditiselegans and other species.

Authors:  A N Nathoo; R A Moeller; B A Westlund; A C Hart
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

5.  Characterization of glutamate-gated chloride channels in the pharynx of wild-type and mutant Caenorhabditis elegans delineates the role of the subunit GluCl-alpha2 in the function of the native receptor.

Authors:  D J Pemberton; C J Franks; R J Walker; L Holden-Dye
Journal:  Mol Pharmacol       Date:  2001-05       Impact factor: 4.436

6.  A mutation in the C. elegans EXP-2 potassium channel that alters feeding behavior.

Authors:  M W Davis; R Fleischhauer; J A Dent; R H Joho; L Avery
Journal:  Science       Date:  1999-12-24       Impact factor: 47.728

7.  The neural circuit for touch sensitivity in Caenorhabditis elegans.

Authors:  M Chalfie; J E Sulston; J G White; E Southgate; J N Thomson; S Brenner
Journal:  J Neurosci       Date:  1985-04       Impact factor: 6.167

8.  RIC-3 enhances functional expression of multiple nicotinic acetylcholine receptor subtypes in mammalian cells.

Authors:  Stuart J Lansdell; Veronica J Gee; Patricia C Harkness; Anne I Doward; Elizabeth R Baker; Alasdair J Gibb; Neil S Millar
Journal:  Mol Pharmacol       Date:  2005-08-24       Impact factor: 4.436

Review 9.  Neuronal substrates of complex behaviors in C. elegans.

Authors:  Mario de Bono; Andres Villu Maricq
Journal:  Annu Rev Neurosci       Date:  2005       Impact factor: 12.449

10.  Regulation of intermuscular electrical coupling by the Caenorhabditis elegans innexin inx-6.

Authors:  Shaolin Li; Joseph A Dent; Richard Roy
Journal:  Mol Biol Cell       Date:  2003-04-04       Impact factor: 4.138

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  21 in total

1.  Report on the 12th symposium on invertebrate neurobiology held 31 August-4 September 2011 at the Balaton Limnological Research Institute of the Hungarian Academy of Sciences, Tihany, Hungary.

Authors:  Lindy Holden-Dye; Robert J Walker
Journal:  Invert Neurosci       Date:  2012-04-06

2.  Investigation of feeding behaviour in C. elegans reveals distinct pharmacological and antibacterial effects of nicotine.

Authors:  M M Kudelska; A Lewis; C T Ng; D A Doyle; L Holden-Dye; V M O'Connor; R J Walker
Journal:  Invert Neurosci       Date:  2018-11-07

Review 3.  Neurobiology of plant parasitic nematodes.

Authors:  Lindy Holden-Dye; R J Walker
Journal:  Invert Neurosci       Date:  2011-05-03

4.  Multiple excitatory and inhibitory neural signals converge to fine-tune Caenorhabditis elegans feeding to food availability.

Authors:  Nicolas Dallière; Nikhil Bhatla; Zara Luedtke; Dengke K Ma; Jonathan Woolman; Robert J Walker; Lindy Holden-Dye; Vincent O'Connor
Journal:  FASEB J       Date:  2015-10-29       Impact factor: 5.191

Review 5.  The regulation of feeding and metabolism in response to food deprivation in Caenorhabditis elegans.

Authors:  Sarah Luedtke; Vincent O'Connor; Lindy Holden-Dye; Robert J Walker
Journal:  Invert Neurosci       Date:  2010-12-01

6.  Distinct molecular targets including SLO-1 and gap junctions are engaged across a continuum of ethanol concentrations in Caenorhabditis elegans.

Authors:  James Dillon; Ioannis Andrianakis; Richard Mould; Ben Ient; Wei Liu; Christopher James; Vincent O'Connor; Lindy Holden-Dye
Journal:  FASEB J       Date:  2013-07-23       Impact factor: 5.191

7.  NLR-1/CASPR Anchors F-Actin to Promote Gap Junction Formation.

Authors:  Lingfeng Meng; Dong Yan
Journal:  Dev Cell       Date:  2020-11-24       Impact factor: 12.270

8.  A comparison of electrically evoked and channel rhodopsin-evoked postsynaptic potentials in the pharyngeal system of Caenorhabditis elegans.

Authors:  Christopher J Franks; Caitriona Murray; David Ogden; Vincent O'Connor; Lindy Holden-Dye
Journal:  Invert Neurosci       Date:  2009-03-18

9.  Mesoscopic organization reveals the constraints governing Caenorhabditis elegans nervous system.

Authors:  Raj Kumar Pan; Nivedita Chatterjee; Sitabhra Sinha
Journal:  PLoS One       Date:  2010-02-22       Impact factor: 3.240

10.  AutoEPG: software for the analysis of electrical activity in the microcircuit underpinning feeding behaviour of Caenorhabditis elegans.

Authors:  James Dillon; Ioannis Andrianakis; Kate Bull; Steve Glautier; Vincent O'Connor; Lindy Holden-Dye; Christopher James
Journal:  PLoS One       Date:  2009-12-29       Impact factor: 3.240

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