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Bcl-2 and Bax mammalian regulators of apoptosis are functional in Drosophila

Authors :
Isabelle Guénal
L Théodore
Sébastien Gaumer
Sylvain Brun
Bernard Mignotte
Mignotte, Bernard
Laboratoire de génétique et biologie cellulaire (LGBC)
Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Source :
HAL, Scopus-Elsevier, Cell Death and Differentiation, Cell Death and Differentiation, Nature Publishing Group, 2000, Cell Death and Disease, Cell Death and Disease, Nature Publishing Group, 2000
Publication Year :
2000
Publisher :
HAL CCSD, 2000.

Abstract

International audience; Studies of apoptosis in C. elegans have allowed the identification of three genes, ced-3, ced-4 and ced-9. Their products constitute the components of an induction pathway of apoptosis conserved in the nematode and mammals. In Drosophila, homologues have been found for CED-3, CED-4 and CED-9. CED-9 belongs to the Bcl-2 family which includes negative (Bcl-2) and positive (Bax) regulators of apoptosis. The recently discovered Bcl-2 family member named Drob-1 acts as a positive regulator of cell death. To address whether a Bcl-2 anti-apoptotic pathway exists in the fly, we studied the effects of expressing the mammalian genes bcl-2 in Drosophila. In embryos, expression of bcl-2 inhibits developmental and X-ray-induced apoptosis. Expressing bcl-2 or the pro-apoptotic mammalian bax in the developing eye and wing alters these structures, bcl-2 increasing the number of cells, while bax reduces the number of cells. In addition, the functional interaction between Bcl-2 and Bax is conserved. These results indicate that factors necessary for the activity of bcl-2 and bax are present in Drosophila. Therefore, a Bcl-2 pathway for inhibition of cell death may exist in the fly. Cell Death and Differentiation (2000) 7, 804 ± 814.

Details

Language :
English
ISSN :
13509047, 14765403, and 20414889
Database :
OpenAIRE
Journal :
HAL, Scopus-Elsevier, Cell Death and Differentiation, Cell Death and Differentiation, Nature Publishing Group, 2000, Cell Death and Disease, Cell Death and Disease, Nature Publishing Group, 2000
Accession number :
edsair.doi.dedup.....a7114028e6ac7463b985b6a56b6879e6