4.6 Article

The Caenorhabditis elegans unc-63 gene encodes a Levamisole-sensitive nicotinic acetylcholine receptor α subunit

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 279, 期 41, 页码 42476-42483

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M404370200

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资金

  1. Medical Research Council [MC_U137761447] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS041477-03, R01 NS041477-01A1, R01 NS041477-02, R01 NS041477] Funding Source: Medline
  3. Medical Research Council [MC_U137761447] Funding Source: researchfish
  4. MRC [MC_U137761447] Funding Source: UKRI

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The anthelmintic drug levamisole causes hypercontraction of body wall muscles and lethality in nematode worms. In the nematode Caenorhabditis elegans, a genetic screen for levamisole resistance has identified 12 genes, three of which (unc-38, unc-29, and lev-1) encode nicotinic acetylcholine receptor (nAChR) subunits. Here we describe the molecular and functional characterization of another levamisole-resistant gene, unc-63, encoding a nAChR alpha subunit with a predicted amino acid sequence most similar to that of UNC-38. Like UNC-38 and UNC-29, UNC-63 is expressed in body wall muscles. In addition, UNC-63 is expressed in vulval muscles and neurons. We also show that LEV-1 is expressed in body wall muscle, thus overlapping the cellular localization of UNC-63, UNC-38, and UNC-29 and suggesting possible association in vivo. This is supported by electrophysiological studies on body wall muscle, which demonstrate that a levamisole-sensitive nAChR present at the C. elegans neuromuscular junction requires both UNC-63 and LEV-1 subunits. Thus, at least four subunits, two alpha types (UNC-38 and UNC-63) and two non-alpha types (UNC-29 and LEV-1), can contribute to levamisole-sensitive muscle nAChRs in nematodes.

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