A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

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Reference
Citation Chen, G.C., Lee, J.Y., Tang, H.W., Debnath, J., Thomas, S.M., Settleman, J. (2008). Genetic interactions between Drosophila melanogaster Atg1 and paxillin reveal a role for paxillin in autophagosome formation.  Autophagy 4(1): 37--45. (Export to RIS)
FlyBase ID FBrf0203068
Publication Type Research paper
PubMed ID 17952025
PubMed Abstract Autophagy is a conserved cellular process of macromolecule recycling that involves vesicle-mediated degradation of cytoplasmic components. Autophagy plays essential roles in normal cell homeostasis and development, the response to stresses such as nutrient starvation, and contributes to disease processes including cancer and neurodegeneration. Although many of the autophagy components identified from genetic screens in yeast are well conserved in higher organisms, the mechanisms by which this process is regulated in any species are just beginning to be elucidated. In a genetic screen in Drosophila melanogaster, we have identified a link between the focal adhesion protein paxillin and the Atg1 kinase, which has been previously implicated in autophagy. In mammalian cells, we find that paxillin is redistributed from focal adhesions during nutrient deprivation, and paxillin-deficient cells exhibit defects in autophagosome formation. Together, these findings reveal a novel evolutionarily conserved role for paxillin in autophagy.
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Language of Publication English
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Publication Type Journal
Abbreviation Autophagy
Title Autophagy
Publication Year 2005-
ISBN/ISSN 1554-8627 1554-8635
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