4.6 Article

dGIPC is required for the locomotive activity and longevity in Drosophila

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2010.10.095

Keywords

P element mutagenesis; Central nervous system; Lifespan; Glia; PDZ domain; Drosophila

Funding

  1. Korea Ministry of Science and Technology [M10412000086-04N1200-08610]
  2. Korea Science and Engineering Foundation [R01-2006-000-10783]
  3. Korean Research Foundation [KRF-2008-313-000643]

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To identify genes that function in the adult neural system, we screened pools of P element-mediated mutants and tested locomotor activity of homozygous flies Of 1014 P element-mutagenized lines, 638 were homozygous viable These lines were tested for climbing ability and lifespan We isolated dGIPC. a Drosophila homolog of WC, that produced a 50% premature loss of locomotor activity and a 30% reduction in life span We found that dGIPC is expressed in the central brain of adult flies, especially in glia and dopaminergic (DA) neurons. Inhibition of dGIPC expression in DA neurons significantly affected climbing ability and survival In vertebrates, interactions between GIPC with dopamine receptors have been reported Our findings, together with those obtained from vertebrate models, suggest that Drosophila dGIPC acts in the adult central nervous system and may be required to regulate the trafficking of dopamine receptors needed for proper functioning of dopaminergic neurons (C) 2010 Published by Elsevier Inc

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