Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/111113
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Type: Journal article
Title: Proteome analysis of Drosophila mutants identifies a regulatory role for 14-3-3ε in metabolic pathways
Other Titles: Proteome analysis of Drosophila mutants identifies a regulatory role for 14-3-3epsilon in metabolic pathways
Author: Ng, Y.
Sorvina, A.
Bader, C.
Weiland, F.
Lopez, A.
Hoffmann, P.
Shandala, T.
Brooks, D.
Citation: Journal of Proteome Research, 2017; 16(5):1976-1987
Publisher: American Chemical Society
Issue Date: 2017
ISSN: 1535-3893
1535-3907
Statement of
Responsibility: 
Yeap S. Ng, Alexandra Sorvina, Christie A. Bader, Florian Weiland, Angel F. Lopez, Peter Hoffmann, Tetyana Shandala, and Douglas A. Brooks
Abstract: The evolutionary conserved family of 14-3-3 proteins appears to have a role in integrating numerous intracellular pathways, including signal transduction, intracellular trafficking, and metabolism. However, little is known about how this interactive network might be affected by the direct abrogation of 14-3-3 function. The loss of Drosophila 14-3-3ε resulted in reduced survival of mutants during larval-to-adult transition, which is known to depend on an energy supply coming from the histolysis of fat body tissue. Here we report a differential proteomic analysis of larval fat body tissue at the onset of larval-to-adult transition, with the loss of 14-3-3ε resulting in the altered abundance of 16 proteins. These included proteins linked to protein biosynthesis, glycolysis, tricarboxylic acid cycle, and lipid metabolic pathways. The ecdysone receptor (EcR), which is responsible for initiating the larval-to-adult transition, colocalized with 14-3-3ε in wild-type fat body tissues. The altered protein abundance in 14-3-3ε mutant fat body tissue was associated with transcriptional deregulation of alcohol dehydrogenase, fat body protein 1, and lamin genes, which are known targets of the EcR. This study indicates that 14-3-3ε has a critical role in cellular metabolism involving either molecular crosstalk with the EcR or direct interaction with metabolic proteins.
Keywords: 14−3−3ε mutants; proteomics; ecdysone receptor; fat body protein 1; alcohol dehydrogenase; lamin
Rights: © 2017 American Chemical Society
RMID: 0030077961
DOI: 10.1021/acs.jproteome.6b01032
Grant ID: http://purl.org/au-research/grants/nhmrc/631915
Appears in Collections:Medical Sciences publications

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