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      An ion channel of the degenerin/epithelial sodium channel superfamily controls the defecation rhythm in Caenorhabditis elegans.

      Proceedings of the National Academy of Sciences of the United States of America
      Activity Cycles, genetics, Amino Acid Sequence, Animals, Base Sequence, Caenorhabditis elegans, growth & development, physiology, Cloning, Molecular, DNA Primers, Defecation, drug effects, Fluorides, pharmacology, Genes, Helminth, Genes, Reporter, Green Fluorescent Proteins, Intestines, embryology, Ion Channels, Luminescent Proteins, Molecular Sequence Data, Mutation, Phenotype, Polymerase Chain Reaction, Sequence Homology, Amino Acid, Sodium Channels

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          Abstract

          Ultradian rhythms are widespread phenomena found in various biological organisms. A typical example is the defecation behavior of the nematode Caenorhabditis elegans, which repeats at about 45-sec intervals. To elucidate the mechanism, we studied flr-1 mutants, which show very short defecation cycle periods. The mutations also affect some food-related functions, including growth rate, the expulsion step of defecation behavior, and the regulation of the dauer larva (a nonfeeding, special third-stage larva) formation in the unc-3 (Olf-1/EBF homolog) background. The flr-1 gene encodes a novel ion channel belonging to the DEG/ENaC (C. elegans degenerin and mammalian epithelial sodium channel) superfamily. A flr-1::GFP (green fluorescent protein) fusion gene that can rescue the flr-1 mutant phenotypes is expressed only in the intestine from embryos to adults. These results suggest that FLR-1 may be a component of an intestinal regulatory system that controls the defecation rhythm as well as other functions.

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