Literature DB >> 8342028

The Caenorhabditis elegans unc-17 gene: a putative vesicular acetylcholine transporter.

A Alfonso1, K Grundahl, J S Duerr, H P Han, J B Rand.   

Abstract

Mutations in the unc-17 gene of the nematode Caenorhabditis elegans produce deficits in neuromuscular function. This gene was cloned and complementary DNAs were sequenced. On the basis of sequence similarity to mammalian vesicular transporters of biogenic amines and of localization to synaptic vesicles of cholinergic neurons in C. elegans, unc-17 likely encodes the vesicular transporter of acetylcholine. Mutations that eliminated all unc-17 gene function were lethal, suggesting that the acetylcholine transporter is essential. Molecular analysis of unc-17 mutations will allow the correlation of specific parts of the gene (and the protein) with observed functional defects. The mutants will also be useful for the isolation of extragenic suppressors, which could identify genes encoding proteins that interact with UNC-17.

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Year:  1993        PMID: 8342028     DOI: 10.1126/science.8342028

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  120 in total

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Journal:  Neurochem Res       Date:  2003-04       Impact factor: 3.996

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Journal:  Mol Biol Cell       Date:  2000-10       Impact factor: 4.138

Review 4.  Vesicular and plasma membrane transporters for neurotransmitters.

Authors:  Randy D Blakely; Robert H Edwards
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-02-01       Impact factor: 10.005

5.  SapTrap, a Toolkit for High-Throughput CRISPR/Cas9 Gene Modification in Caenorhabditis elegans.

Authors:  Matthew L Schwartz; Erik M Jorgensen
Journal:  Genetics       Date:  2016-02-02       Impact factor: 4.562

6.  Extrasynaptic acetylcholine signaling through a muscarinic receptor regulates cell migration.

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Journal:  Proc Natl Acad Sci U S A       Date:  2021-01-05       Impact factor: 11.205

7.  Constitutive secretion of exogenous neurotransmitter by nonneuronal cells: implications for neuronal secretion.

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

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Journal:  Invert Neurosci       Date:  2009-03-18

9.  Neuroligin-deficient mutants of C. elegans have sensory processing deficits and are hypersensitive to oxidative stress and mercury toxicity.

Authors:  Jerrod W Hunter; Gregory P Mullen; John R McManus; Jessica M Heatherly; Angie Duke; James B Rand
Journal:  Dis Model Mech       Date:  2010-01-18       Impact factor: 5.758

10.  A novel strategy for cell-autonomous gene knockdown in Caenorhabditis elegans defines a cell-specific function for the G-protein subunit GOA-1.

Authors:  Kathryn N Maher; Aishwarya Swaminathan; Parth Patel; Daniel L Chase
Journal:  Genetics       Date:  2013-03-22       Impact factor: 4.562

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