Literature DB >> 8462849

The genetics of feeding in Caenorhabditis elegans.

L Avery1.   

Abstract

The pharynx of Caenorhabditis elegans is a nearly self-contained neuromuscular organ responsible for feeding. To identify genes involved in the development or function of the excitable cells of the pharynx, I screened for worms with visible defects in pharyngeal feeding behavior. Fifty-two mutations identified 35 genes, at least 22 previously unknown. The genes broke down into three broad classes: 2 pha genes, mutations in which caused defects in the shape of the pharynx, 7 phm genes, mutations in which caused defects in the contractile structures of the pharyngeal muscle, and 26 eat genes, mutants in which had abnormal pharyngeal muscle motions, but had normally shaped and normally birefringent pharynxes capable of vigorous contraction. Although the Eat phenotypes were diverse, most resembled those caused by defects in the pharyngeal nervous system. For some of the eat genes there is direct evidence from previous genetic mosaic and pharmacological studies that they do in fact affect nervous system. In eat-5 mutants the motions of the different parts of the pharynx were poorly synchronized. eat-6 and eat-12 mutants failed to relax their pharyngeal muscles properly. These pharyngeal motion defects are most easily explained as resulting from abnormal electrical excitability of the pharyngeal muscle membrane.

Entities:  

Mesh:

Year:  1993        PMID: 8462849      PMCID: PMC1205408     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  39 in total

1.  Control of larval development by chemosensory neurons in Caenorhabditis elegans.

Authors:  C I Bargmann; H R Horvitz
Journal:  Science       Date:  1991-03-08       Impact factor: 47.728

2.  Cellular interactions in early C. elegans embryos.

Authors:  J R Priess; J N Thomson
Journal:  Cell       Date:  1987-01-30       Impact factor: 41.582

3.  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

4.  Male Phenotypes and Mating Efficiency in CAENORHABDITIS ELEGANS.

Authors:  J Hodgkin
Journal:  Genetics       Date:  1983-01       Impact factor: 4.562

5.  Sensory control of dauer larva formation in Caenorhabditis elegans.

Authors:  P S Albert; S J Brown; D L Riddle
Journal:  J Comp Neurol       Date:  1981-05-20       Impact factor: 3.215

6.  Developmental genetics of the mechanosensory neurons of Caenorhabditis elegans.

Authors:  M Chalfie; J Sulston
Journal:  Dev Biol       Date:  1981-03       Impact factor: 3.582

7.  Genetic organization of the region around UNC-15 (I), a gene affecting paramyosin in Caenorhabditis elegans.

Authors:  A M Rose; D L Baillie
Journal:  Genetics       Date:  1980-11       Impact factor: 4.562

8.  The genetics of Caenorhabditis elegans.

Authors:  S Brenner
Journal:  Genetics       Date:  1974-05       Impact factor: 4.562

9.  Voltage-clamp analysis of the potassium current that produces a negative-going action potential in Ascaris muscle.

Authors:  L Byerly; M O Masuda
Journal:  J Physiol       Date:  1979-03       Impact factor: 5.182

10.  The minor myosin heavy chain, mhcA, of Caenorhabditis elegans is necessary for the initiation of thick filament assembly.

Authors:  R H Waterston
Journal:  EMBO J       Date:  1989-11       Impact factor: 11.598

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  224 in total

1.  eat-11 encodes GPB-2, a Gbeta(5) ortholog that interacts with G(o)alpha and G(q)alpha to regulate C. elegans behavior.

Authors:  M Robatzek; T Niacaris; K Steger; L Avery; J H Thomas
Journal:  Curr Biol       Date:  2001-02-20       Impact factor: 10.834

2.  Dauer formation induced by high temperatures in Caenorhabditis elegans.

Authors:  M Ailion; J H Thomas
Journal:  Genetics       Date:  2000-11       Impact factor: 4.562

3.  Phenotypic and suppressor analysis of defecation in clk-1 mutants reveals that reaction to changes in temperature is an active process in Caenorhabditis elegans.

Authors:  R Branicky; Y Shibata; J Feng; S Hekimi
Journal:  Genetics       Date:  2001-11       Impact factor: 4.562

4.  Food transport in the C. elegans pharynx.

Authors:  Leon Avery; Boris B Shtonda
Journal:  J Exp Biol       Date:  2003-07       Impact factor: 3.312

5.  EAT-20, a novel transmembrane protein with EGF motifs, is required for efficient feeding in Caenorhabditis elegans.

Authors:  Y Shibata; T Fujii; J A Dent; H Fujisawa; S Takagi
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

6.  A new group-training procedure for habituation demonstrates that presynaptic glutamate release contributes to long-term memory in Caenorhabditis elegans.

Authors:  Jacqueline K Rose; Karla R Kaun; Catharine H Rankin
Journal:  Learn Mem       Date:  2002 May-Jun       Impact factor: 2.460

7.  Isolation and characterization of high-temperature-induced Dauer formation mutants in Caenorhabditis elegans.

Authors:  Michael Ailion; James H Thomas
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

8.  Measurements of age-related changes of physiological processes that predict lifespan of Caenorhabditis elegans.

Authors:  Cheng Huang; Chengjie Xiong; Kerry Kornfeld
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-12       Impact factor: 11.205

9.  Chemosensory cue conditioning with stimulants in a Caenorhabditis elegans animal model of addiction.

Authors:  Heather N Musselman; Bethany Neal-Beliveau; Richard Nass; Eric A Engleman
Journal:  Behav Neurosci       Date:  2012-06       Impact factor: 1.912

10.  Starvation activates MAP kinase through the muscarinic acetylcholine pathway in Caenorhabditis elegans pharynx.

Authors:  Young-jai You; Jeongho Kim; Melanie Cobb; Leon Avery
Journal:  Cell Metab       Date:  2006-04       Impact factor: 27.287

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