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Originally published In Press as doi:10.1074/jbc.M010419200 on January 29, 2001

J. Biol. Chem., Vol. 276, Issue 19, 16240-16247, May 11, 2001
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Neuron-specific Bcl-2 Homology 3 Domain-only Splice Variant of Bak Is Anti-apoptotic in Neurons, but Pro-apoptotic in Non-neuronal Cells*

Yun-Fu Sun, Li-Ying Yu, Mart SaarmaDagger , Tõnis Timmusk, and Urmas Arumäe§

From the Program of Molecular Neurobiology, Institute of Biotechnology, University of Helsinki, Viikki Biocenter, FIN-00014 Helsinki, Finland

We have identified and characterized N-Bak, a neuron-specific isoform of the pro-apoptotic Bcl-2 family member Bak. N-Bak is generated by neuron-specific splicing of a novel 20-base pair exon, which changes the previously described Bak, containing Bcl-2 homology (BH) domains BH1, BH2, and BH3, into a shorter BH3-only protein. As demonstrated by reverse transcription-polymerase chain reaction and RNase protection assay, N-Bak transcripts are expressed only in central and peripheral neurons, but not in other cells, whereas the previously described Bak is expressed ubiquitously, but not in neurons. Neonatal sympathetic neurons microinjected with N-Bak resisted apoptotic death caused by nerve growth factor (NGF) removal, whereas microinjected Bak accelerated NGF deprivation-induced death. Overexpressed Bak killed sympathetic neurons in the presence of NGF, whereas N-Bak did not. N-Bak was, however, still death-promoting when overexpressed in non-neuronal cells. Thus, N-Bak is an anti-apoptotic BH3-only protein, but only in the appropriate cellular environment. This is the first example of a neuron-specific Bcl-2 family member.


* This work was supported by Academy of Finland Programs 44896 (Finnish Center of Excellence Program 2000-2005) and 43679, European Union Biotech Grant BIO4-98-0293, and a Sigrid Jusélius Foundation grant.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger A Biocentrum Helsinki Fellow.

§ To whom correspondence should be addressed: Program of Molecular Neurobiology, Inst. of Biotechnology, University of Helsinki, P. O. Box 56, Viikki Biocenter, FIN-00014 Helsinki, Finland. Tel.: 358-9-19159369; Fax: 358-9-19159366; E-mail: urmas.arumae@helsinki.fi.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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