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A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia.

A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Research Abstract Details 

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  • A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Abstract Text:

    john a humphreyJohn A Humphrey,kevin s hammingKevin S Hamming,colin m thackerColin M Thacker,robert l scottRobert L Scott,margaret m sedenskyMargaret M Sedensky,terrance p snutchTerrance P Snutch,phil g morganPhil G Morgan,howard a nashHoward A Nash,

    Volatile anesthetics like halothane and enflurane are of interest to clinicians and neuroscientists because of their ability to preferentially disrupt higher functions that make up the conscious state. All volatiles were once thought to act identically; if so, they should be affected equally by genetic variants. However, mutations in two distinct genes, one in Caenorhabditis and one in Drosophila, have been reported to produce much larger effects on the response to halothane than enflurane [1, 2]. To see whether this anesthesia signature is adventitious or fundamental, we have identified orthologs of each gene and determined the mutant phenotype within each species. The fly gene, narrow abdomen (na), encodes a putative ion channel whose sequence places it in a unique family; the nematode gene, unc-79, is identified here as encoding a large cytosolic protein that lacks obvious motifs. In Caenorhabditis, mutations that inactivate both of the na orthologs produce an Unc-79 phenotype; in Drosophila, mutations that inactivate the unc-79 ortholog produce an na phenotype. In each organism, studies of double mutants place the genes in the same pathway, and biochemical studies show that proteins of the UNC-79 family control NA protein levels by a posttranscriptional mechanism. Thus, the anesthetic signature reflects an evolutionarily conserved role for the na orthologs, implying its intimate involvement in drug action.

    A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Publishing Authors By Initials

    ja humphreyJA Humphrey,ks hammingKS Hamming,cm thackerCM Thacker,rl scottRL Scott,mm sedenskyMM Sedensky,tp snutchTP Snutch,pg morganPG Morgan,ha nashHA Nash,

    For similar genetic phenomena: phenotype research abstracts see: genetic phenomena: phenotype research

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    A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Current biology : CB

    VOLUME: 17

    Page Numbers: 624-9

    Journal Abbreviation: Curr. Biol.

    ISSN: 0960-9822

    DAY: 15

    MONTH: 03

    YEAR: 2007

    A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9107782

    A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Keywords Mesh Terms:

    KEYWORDS: Phenotype

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia. Information

    Substance Name: Halothane

    Registry Number: 151-67-7

    Grant and Affiliation Information for A putative cation channel and its novel regulator: cross-species conservation of effects on general anesthesia.

    AFFILIATION: Department of Genetics, Case Medical Center, Cleveland, OH 44106, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NIGMS

    GRANT: T32 GM008613

    ACRONYM: GM

    MEDLINETA: Curr Biol

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