Given the increasing evidence that RNA binding proteins (RBPs) serve as genetic causes or predisposing risk factors underlying a wide spectrum of neurological diseases, a pressing need exists to understand their specific cellular functions in developing and mature brains. Similar to transcription factors, RBPs could be master regulators of certain cellular processes owing to their coordinated target sets. Unlike widely-studied transcription factors, the physiological functions of RBPs are historically underexplored. Most of the dozen RBPs found to exhibit tissue-specific expression are involved in regulating neuronal alternative splicing. We and others have revealed the large-scale genetic programming of alternative splicing during embryonic brain development, resulting in neuron-specific alternative isoforms in mature brains. We show many of these splicing changes are mediated by a nuclear RBP, polypyrimidine tract-binding protein 2 (PTBP2). PTBP2 exhibits dynamic temporal expression during neuronal differentiation and may orchestrate the developmental programming of alternative splicing in order to accomplish the prolonged and continuous neuronal morphological transformations. Our previous study shows that downregulation of PTBP2 prior to synaptogenesis is necessary for spine formation. Our newest data show that PTBP2 has additional functions in early differentiating neurons prior to synapse formation. Guided by strong preliminary data, we hypothesize that PTBP2 governs neuron-specific splicing to control the initiation of neuronal polarity. This proposal will address multiple critical barriers to the study of neuronal polarity and provide a new framework for functional analysis of alternative splicing. Our long history of researching alternative splicing and PTBP2 in the brain places us in a unique position to advance these fields. Our team, with complementary expertise in genetics, neurobiology, and molecular cellular biochemical and computational biology, has demonstrated successful collaborations. We have generated new tools and resource to thoroughly determine the cellular and molecular defects caused by Ptbp2 knockout in cortical neurons. Completion of this project will allow us to further our long-term goal of revealing new genetic, molecular and cellular controls of neuronal polarity and morphogenesis that enables neural circuit formation.

Public Health Relevance

The proposed research is relevant to public health because it will begin to dissect the regulation and function of neuron-specific splicing. Many human disease mutations alter splicing to produce aberrant mRNAs and proteins, and mis-regulation of alternative splicing contributes to many brain disorders. Our findings will inform strategies of neuronal repair and regenerative medicine as well as solutions for tackling neurodevelopmental and neurologic disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS104041-01
Application #
9426249
Study Section
Neurodifferentiation, Plasticity, and Regeneration Study Section (NDPR)
Program Officer
Riddle, Robert D
Project Start
2017-12-15
Project End
2022-11-30
Budget Start
2017-12-15
Budget End
2018-11-30
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Type
Schools of Medicine
DUNS #
627797426
City
Riverside
State
CA
Country
United States
Zip Code
92521