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Screening of suppressors of bax-induced cell death identifies glycerophosphate oxidase-1 as a mediator of debcl-induced apoptosis in Drosophila

Title: Screening of suppressors of bax-induced cell death identifies glycerophosphate oxidase-1 as a mediator of debcl-induced apoptosis in Drosophila
Authors: Colin, Jessie; Garibal, Julie; Clavier, Amandine; Szuplewski, Sébastien; Risler, Yanick; Milet, Cécile; Gaumer, Sébastien; Guénal, Isabelle; Mignotte, Bernard
Contributors: Laboratoire de génétique et biologie cellulaire (LGBC); Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-École Pratique des Hautes Études (EPHE); Université Paris Sciences et Lettres (PSL)-Université Paris Sciences et Lettres (PSL)
Source: EISSN: 1947-6027 ; Genes and Cancer ; https://uvsq.hal.science/hal-02975511 ; Genes and Cancer, 2015, 6, ⟨10.18632/genesandcancer.68⟩
Publisher Information: CCSD; SAGE Publications
Publication Year: 2015
Collection: Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQ
Subject Terms: Bax; Glycerophosphate oxidase; Debcl; mutagenesis; Apoptosis; [SDV]Life Sciences [q-bio]
Description: International audience ; Members of the Bcl-2 family are key elements of the apoptotic machinery. In mammals, this multigenic family contains about twenty members, which either promote or inhibit apoptosis. We have previously shown that the mammalian pro-apoptotic Bcl-2 family member Bax is very efficient in inducing apoptosis in Drosophila, allowing the study of bax-induced cell death in a genetic animal model. We report here the results of the screening of a P[UAS]-element insertion library performed to identify gene products that modify the phenotypes induced by the expression of bax in Drosophila melanogaster. We isolated 17 putative modifiers involved in various function or process: the ubiquitin/proteasome pathway; cell growth, proliferation and death; pathfinding and cell adhesion; secretion and extracellular signaling; metabolism and oxidative stress. Most of these suppressors also inhibit debcl-induced phenotypes, suggesting that the activities of both proteins can be modulated in part by common signaling or metabolic pathways. Among these suppressors, Glycerophosphate oxidase-1 is found to participate in debcl-induced apoptosis by increasing mitochondrial reactive oxygen species accumulation.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/26124923; PUBMED: 26124923
DOI: 10.18632/genesandcancer.68
Availability: https://uvsq.hal.science/hal-02975511; https://uvsq.hal.science/hal-02975511v1/document; https://uvsq.hal.science/hal-02975511v1/file/Genes%20Cancer%202015_JColin.pdf; https://doi.org/10.18632/genesandcancer.68
Rights: info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.BB792F16
Database: BASE