Literature DB >> 10340851

The multifunctional Drosophila melanogaster V-ATPase is encoded by a multigene family.

J A Dow1.   

Abstract

In animals, V-ATPases are believed to play roles in the plasma membrane, as well as endomembrane. To understand these different functions, it is necessary to adopt a genetic approach in a physiologically tractable model organism. For this purpose, Drosophila melanogaster is ideal, because of the powerful genetics associated with the organism and because of the unusually informative epithelial phenotype provided by the Malpighian tubule. Recently, the first animal "knockouts" of a V-ATPase were described in Drosophila. The resulting phenotypes have general utility for our understanding of V-ATPase function and suggest a screen for novel subunits and associated proteins. Genome project resources have accelerated our knowledge of the V-ATPase gene family size and the new Drosophila genes vhaSFD, vha100-1, vha100-2, vha100-3, vha16-2, vha16-3, vha16-4, vhaPPA1, vhaPPA2, vhaM9.7.1, and vhaM9.7.2 are described. The Drosophila V-ATPase model is thus well-suited to both forward and reverse genetic analysis of this complex multifunctional enzyme.

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Year:  1999        PMID: 10340851     DOI: 10.1023/a:1005400731289

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  12 in total

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7.  Transient receptor potential-like channels are essential for calcium signaling and fluid transport in a Drosophila epithelium.

Authors:  Matthew R MacPherson; Valerie P Pollock; Laura Kean; Tony D Southall; Maria E Giannakou; Kate E Broderick; Julian A T Dow; Roger C Hardie; Shireen A Davies
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8.  Functional genomic screen and network analysis reveal novel modifiers of tauopathy dissociated from tau phosphorylation.

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10.  Function-informed transcriptome analysis of Drosophila renal tubule.

Authors:  Jing Wang; Laura Kean; Jingli Yang; Adrian K Allan; Shireen A Davies; Pawel Herzyk; Julian A T Dow
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