A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Goyal, G., Fell, B., Sarin, A., Youle, R.J., Sriram, V. (2007). Role of mitochondrial remodeling in programmed cell death in Drosophila melanogaster.  Dev. Cell 12(5): 807--816. (Export to RIS)
FlyBase ID FBrf0202254
Publication Type Research paper
PubMed ID 17488630
PubMed Abstract The role of mitochondria in Drosophila programmed cell death remains unclear, although certain gene products that regulate cell death seem to be evolutionarily conserved. We find that developmental programmed cell death stimuli in vivo and multiple apoptotic stimuli ex vivo induce dramatic mitochondrial fragmentation upstream of effector caspase activation, phosphatidylserine exposure, and nuclear condensation in Drosophila cells. Unlike genotoxic stress, a lipid cell death mediator induced an increase in mitochondrial contiguity prior to fragmentation of the mitochondria. Using genetic mutants and RNAi-mediated knockdown of drp-1, we find that Drp-1 not only regulates mitochondrial fission in normal cells, but mediates mitochondrial fragmentation during programmed cell death. Mitochondria in drp-1 mutants fail to fragment, resulting in hyperplasia of tissues in vivo and protection of cells from multiple apoptotic stimuli ex vivo. Thus, mitochondrial remodeling is capable of modifying the propensity of cells to undergo death in Drosophila.
DOI 10.1016/j.devcel.2007.02.002
Related Publication(s)
Review Torn to pieces.
Anonymous, 2007, Nature 447(7143): 357 [FBrf0202546]

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Language of Publication English
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Publication Type Journal
Abbreviation Dev. Cell
Title Developmental Cell
Publication Year 2001-
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