Literature DB >> 10488330

Fluoxetine-resistant mutants in C. elegans define a novel family of transmembrane proteins.

R K Choy1, J H Thomas.   

Abstract

Fluoxetine (Prozac) is an antidepressant that is thought to act by blocking presynaptic reuptake of the neurotransmitter serotonin. Despite widespread clinical use of fluoxetine, direct evidence for this mechanism has been difficult to obtain in vivo. We have determined that fluoxetine has an additional neuromuscular effect on C. elegans that is distinct from inhibition of serotonin reuptake. By screening for mutants resistant to this effect, we have identified seven genes. We report that two of these genes are homologous to each other and define a novel gene family that encodes over a dozen multipass transmembrane proteins. Our findings may have clinical implications for the mechanism of action of fluoxetine.

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Year:  1999        PMID: 10488330     DOI: 10.1016/s1097-2765(00)80362-7

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  39 in total

1.  Nutrient control of gene expression in Drosophila: microarray analysis of starvation and sugar-dependent response.

Authors:  Ingo Zinke; Christina S Schütz; Jörg D Katzenberger; Matthias Bauer; Michael J Pankratz
Journal:  EMBO J       Date:  2002-11-15       Impact factor: 11.598

2.  Developmental expression of drop-dead is required for early adult survival and normal body mass in Drosophila melanogaster.

Authors:  Christine Lynn Sansone; Edward M Blumenthal
Journal:  Insect Biochem Mol Biol       Date:  2012-06-21       Impact factor: 4.714

3.  Fluoxetine-resistance genes in Caenorhabditis elegans function in the intestine and may act in drug transport.

Authors:  Robert K M Choy; John M Kemner; James H Thomas
Journal:  Genetics       Date:  2005-08-22       Impact factor: 4.562

4.  Chemical genetics: reshaping biology through chemistry.

Authors:  Stefan Florian; Stefan Hümmer; Mario Catarinella; Thomas U Mayer
Journal:  HFSP J       Date:  2007-07-12

5.  Deleterious Consequences of UDP-Galactopyranose Mutase Inhibition for Nematodes.

Authors:  Valerie J Winton; Alexander M Justen; Helen Deng; Laura L Kiessling
Journal:  ACS Chem Biol       Date:  2017-08-16       Impact factor: 5.100

6.  A Caenorhabditis elegans p38 MAP kinase pathway mutant protects from dopamine, methamphetamine, and MDMA toxicity.

Authors:  Matthew A Schreiber; Steven L McIntire
Journal:  Neurosci Lett       Date:  2011-05-05       Impact factor: 3.046

Review 7.  Pharming for Genes in Neurotransmission: Combining Chemical and Genetic Approaches in Caenorhabditis elegans.

Authors:  Stephen M Blazie; Yishi Jin
Journal:  ACS Chem Neurosci       Date:  2018-03-06       Impact factor: 4.418

Review 8.  Using C. elegans to decipher the cellular and molecular mechanisms underlying neurodevelopmental disorders.

Authors:  Carlos Bessa; Patrícia Maciel; Ana João Rodrigues
Journal:  Mol Neurobiol       Date:  2013-03-14       Impact factor: 5.590

9.  The Caenorhabditis elegans germ line regulates distinct signaling pathways to control lifespan and innate immunity.

Authors:  Scott Alper; Matthew K McElwee; Javier Apfeld; Brad Lackford; Jonathan H Freedman; David A Schwartz
Journal:  J Biol Chem       Date:  2009-11-18       Impact factor: 5.157

10.  Dietary manipulation implicates lipid signaling in the regulation of germ cell maintenance in C. elegans.

Authors:  Jennifer L Watts; John Browse
Journal:  Dev Biol       Date:  2006-02-17       Impact factor: 3.582

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