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J. Biol. Chem., Vol. 276, Issue 19, 16240-16247, May 11, 2001
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,
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.
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.
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