Our long-term objective is to understand the relationship between cell proliferation and the initiation of terminal differentiation in the nervous system. In this study, we seek to understand the molecular mechanism of how a protein kinase that shares striking structural homology to kinases that are essential for cell division functions during neuronal differentiation. Cyclin-dependent kinase 5, a close homologue of cdk2 and cdc2, displays associated kinase activity only in the nervous system of adult mammals. During embryonic development, cdk5 kinase activity parallels the advance of neurogenesis. The unique temporal and spatial patterns of cdk5 activity are due in part, to the distribution of its regulatory partner p35. p35 is a novel cdk activator that associates with cdk5 in post-mitotic neurons. This association gives rise to active kinase in the absence of other protein molecules. Surprisingly, the primary sequence of p35 does not share any homology to known cyclins or other protein molecules in the database. During mouse embryonic development p35 mRNA appears immediately after neurons exit the cell cycle and is transiently expressed in post- mitotic neurons of the central nervous system (CNS). These observations indicate that the cdk5/p35 kinase is likely to play an important role in neurogenesis of the CNS during embryonic development. Indeed, we find that overexpression of a dominant negative form of cdk5 or antisense p35 inhibited neurite outgrowth in differentiating cultured cortical neurons. Conversely, co-expression of wildtype cdk5 and p35 enhanced neurite outgrowth. This research proposal has two aims; 1) To investigate the regulation of cdk5 kinase activity by p35. The minimal region(s) of p35 that is sufficient for association and activation of cdk5 will be determined. Also residues on cdk5 that allow its specificity to p35 will be defined. These experiments are likely to shed light on a novel activation mechanism of a cdk by its regulatory partner. 2) To further explore the biological function of the cdk5/p35 kinase in neurogenesis. Using the approach of overexpressing mutant and wildtype cdk5/p35 kinase in primary cortical cultures, we have shown that the cdk5/p35 kinase plays a role in neurite outgrowth. This system will be used to characterize the changes in neuronal differentiation that caused by the elevation or inactivation of cdk5/p35 kinase and to investigate a role of this kinase in the onset of neuronal differentiation. In a complementary approach, the consequence of loss of p35 function in mice will be analyzed. The phenotype displayed by animals homozygous for a deletion of the p35 gene will indicate stages of neurogenesis that require p35. The combination of in vitro and in vivo approaches will reveal the biological function of the cdk5/p35 kinase.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053049-04
Application #
2900844
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1996-04-01
Project End
2001-03-31
Budget Start
1999-04-01
Budget End
2000-03-31
Support Year
4
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Harvard University
Department
Pathology
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
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Rudenko, Andrii; Dawlaty, Meelad M; Seo, Jinsoo et al. (2013) Tet1 is critical for neuronal activity-regulated gene expression and memory extinction. Neuron 79:1109-1122
Su, Susan C; Seo, Jinsoo; Pan, Jen Q et al. (2012) Regulation of N-type voltage-gated calcium channels and presynaptic function by cyclin-dependent kinase 5. Neuron 75:675-87
Patzke, Holger; Maddineni, Upendra; Ayala, Ramses et al. (2003) Partial rescue of the p35-/- brain phenotype by low expression of a neuronal-specific enolase p25 transgene. J Neurosci 23:2769-78
Patzke, Holger; Tsai, Li-Huei (2002) Calpain-mediated cleavage of the cyclin-dependent kinase-5 activator p39 to p29. J Biol Chem 277:8054-60
Ko, J; Humbert, S; Bronson, R T et al. (2001) p35 and p39 are essential for cyclin-dependent kinase 5 function during neurodevelopment. J Neurosci 21:6758-71
Humbert, S; Lanier, L M; Tsai, L H (2000) Synaptic localization of p39, a neuronal activator of cdk5. Neuroreport 11:2213-6
Humbert, S; Dhavan, R; Tsai, L (2000) p39 activates cdk5 in neurons, and is associated with the actin cytoskeleton. J Cell Sci 113 ( Pt 6):975-83
Kwon, Y T; Tsai, L H; Crandall, J E (1999) Callosal axon guidance defects in p35(-/-) mice. J Comp Neurol 415:218-29
Kwon, Y T; Tsai, L H (1998) A novel disruption of cortical development in p35(-/-) mice distinct from reeler. J Comp Neurol 395:510-22

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