DR Mirna Maarabouni m.m.maarabouni@keele.ac.uk
Regulation of apoptosis by fau revealed by functional expression cloning and antisense expression
Mourtada-Maarabouni, Mirna; Kirkham, Lucy; Farzaneh, Farzin; Williams, Gwyn T
Authors
Lucy Kirkham
Farzin Farzaneh
Gwyn T Williams
Contributors
M. Mourtada-Maarabouni
Other
L. Kirkham
Other
F. Farzanch
Other
G.T. Williams
Other
Abstract
Functional expression cloning is a powerful strategy for identifying critical steps in biological pathways independently of prior assumptions. It is particularly suitable for the identification of molecules crucial to the control of apoptosis. Our screen for sequences suppressing T-cell apoptosis isolated a sequence antisense to fau (Finkel–Biskis–Reilly murine sarcoma virus (FBR-MuSV)-associated ubiquitously expressed gene). The fox gene in FBR murine osteosarcoma virus is also antisense to fau and several reports have indicated that fau displays tumour suppressor and oncogenic properties in different contexts. Our observations indicate that the fau antisense sequence suppresses expression of endogenous fau mRNA and produces resistance to apoptosis induced both by the glucocorticoid analogue dexamethasone' by ultraviolet radiation, and by the anticancer drug cisplatin. In all cases, colony-forming ability is protected, indicating that fau affects the critical events prior to commitment to cell death. Overexpression of fau in the sense orientation induces cell death, which is inhibited both by Bcl-2 and by inhibition of caspases, in line with its proposed role in apoptosis.
Citation
Mourtada-Maarabouni, M., Kirkham, L., Farzaneh, F., & Williams, G. T. (2004). Regulation of apoptosis by fau revealed by functional expression cloning and antisense expression. Oncogene, 23, 9419–9426. https://doi.org/10.1038/sj.onc.1208048
Journal Article Type | Article |
---|---|
Acceptance Date | Jul 20, 2004 |
Online Publication Date | Nov 15, 2004 |
Publication Date | Dec 16, 2004 |
Deposit Date | May 16, 2024 |
Journal | Oncogene |
Print ISSN | 1476-5594 |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 23 |
Pages | 9419–9426 |
ISBN | 09509232 |
DOI | https://doi.org/10.1038/sj.onc.1208048 |
Public URL | https://keele-repository.worktribe.com/output/543800 |
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