The ability of neurons to extend neurites is critical for synaptic formation and neuronal function. However, the molecular basis of neurite extension is largely unknown. To understand this fundamental process, the investigators have focused on the leucine-rich acidic nuclear protein (LANP), a protein that is expressed at particularly high levels in developing neurons from the early postnatal brain, in particular the cerebellum, at a time and location when neurons extend to processes to form functional networks. LANP is a nucleocytoplasmic shuttling protein. In the cytoplasm, LANP binds to all classes of structural microtubule-associated-proteins (MAPs);while in the nucleus LANP regulates transcription by inhibiting histone acetyl transferases (HATs). The investigators'preliminary data inspire the intriguing hypothesis that LANP plays a role in development by a dual role: (a) regulating the expression of genes critical for neurite outgrowth, and (b) modulating the properties of the neuronal cytoskeleton. This application makes use of the LANP null mice that the investigators have generated to address the role of LANP in neurite outgrowth. Defects in neurite outgrowth underlie a number of neurodevelopmental syndromes that negatively impact the life of young children and their care-givers. This application will help us to gain insights into the molecular basis of these disorders.

Public Health Relevance

Defects in proteins that regulate gene expression underlie a number of neurodevelopmental syndromes that negatively impact the quality of life of young patients and their care-givers. The investigators'laboratory is focusing on elucidating the properties of a protein called LANP that appear to play an important role as a regulator of neurite outgrowth.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Small Research Grants (R03)
Project #
1R03HD054612-01A2
Application #
7789230
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Henken, Deborah B
Project Start
2010-05-01
Project End
2012-04-30
Budget Start
2010-05-01
Budget End
2011-04-30
Support Year
1
Fiscal Year
2010
Total Cost
$76,250
Indirect Cost
Name
Northwestern University at Chicago
Department
Neurology
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Kular, Rupinder K; Gogliotti, Rocky G; Opal, Puneet (2010) Cpd-1 null mice display a subtle neurological phenotype. PLoS One 5: