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  3. BCL-2 family member BOK is widely expressed but its loss has only minimal impact in mice
 

BCL-2 family member BOK is widely expressed but its loss has only minimal impact in mice

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Publisher DOI
10.1038/cdd.2011.210
PubMed ID
22281706
Description
BOK/MTD was discovered as a protein that binds to the anti-apoptotic Bcl-2 family member MCL-1 and shares extensive amino-acid sequence similarity to BAX and BAK, which are essential for the effector phase of apoptosis. Therefore, and on the basis of its reported expression pattern, BOK is thought to function in a BAX/BAK-like pro-apoptotic manner in female reproductive tissues. In order to determine the function of BOK, we examined its expression in diverse tissues and investigated the consequences of its loss in Bok(-/-) mice. We confirmed that Bok mRNA is prominently expressed in the ovaries and uterus, but also observed that it is present at readily detectable levels in several other tissues such as the brain and myeloid cells. Bok(-/-) mice were produced at the expected Mendelian ratio, appeared outwardly normal and proved fertile. Histological examination revealed that major organs in Bok(-/-) mice displayed no morphological aberrations. Although several human cancers have somatically acquired copy number loss of the Bok gene and BOK is expressed in B lymphoid cells, we found that its deficiency did not accelerate lymphoma development in Eμ-Myc transgenic mice. Collectively, these results indicate that Bok may have a role that largely overlaps with that of other members of the Bcl-2 family, or may have a function restricted to specific stress stimuli and/or tissues.
Date of Publication
2012
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
en
Contributor(s)
Ke, Francine
Voss, Anne
Kerr, Jeffrey
O'Reilly, Lorraine
Tai, Lin
Echeverry, Nohemy
Institut für Pharmakologie
Bouillet, Philippe
Strasser, Andreas
Kaufmann, Thomasorcid-logo
Institut für Pharmakologie
Additional Credits
Institut für Pharmakologie
Series
Cell death and differentiation
Publisher
Nature Publishing Group
ISSN
1350-9047
Access(Rights)
metadata.only
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