The growth-associated protein, GAP-43, is a neuronal phosphoprotein that is required for the initial establishment and remodeling of neural connections. Work done under our previous grant has demonstrated that GAP-43 gene expression is post- transcriptionally regulated by selective changes in the stability of its mRNA, and that this process depends on the interaction of a highly conserved regulatory element in the mRNA with neuronal- specific RNA-binding proteins. We have recently identified one of these proteins as HuD, the mammalian equivalent of Elav, an RNA-binding protein that is critical for nervous system development in Drosophila. Based upon our preliminary studies, we propose that HuD protects that GAP-43 mRNA against ribonuclease attack, leading to an increase in gene expression and neurite outgrowth. To test this hypothesis, we plan to investigate the mechanism by which HuD controls GAP-43 gene expression at the molecular (Aim 1), cellular (Aim 2), and in vivo levels (Aim 3):
Aim 1 : To study the molecular mechanism by which the RNA-binding protein HuD stabilizes the GAP-43 mRNA. We will use a combination of cell-free mRNA decay assays and RNA- binding studies to examine whether binding of HuD to the GAP-43 mRNA protects this from deadenylation.
Aim 2. To determine the cellular specificity of the effect of HuD on GAP-43 gene expression and neurite outgrowth. These studies will utilize primary neuronal cultures, ES cells and neural cell lines.
Aim 3 : To use genetic manipulation techniques to investigate the relationship between HuD and GAP-43 in vivo. We will make use of transgenic mice and viral vectors to probe HuD's function in vivo. The proposed studies will characterize the role of HuD in the post-transcriptional regulation of the GAP-43 gene. Given the role of GAP-43 in nervous system development and regeneration, the elucidation of regulatory mechanisms controlling its expression have potential applications for the treatment of a broad range of conditions from neurodevelopmental disorders, to brain trauma and spinal cord injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS030255-11
Application #
6539736
Study Section
Special Emphasis Panel (ZRG1-MDCN-1 (04))
Program Officer
Leblanc, Gabrielle G
Project Start
1991-06-01
Project End
2005-05-31
Budget Start
2002-06-01
Budget End
2003-05-31
Support Year
11
Fiscal Year
2002
Total Cost
$257,250
Indirect Cost
Name
University of New Mexico
Department
Neurosciences
Type
Schools of Medicine
DUNS #
829868723
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Oliver, R J; Brigman, J L; Bolognani, F et al. (2018) Neuronal RNA-binding protein HuD regulates addiction-related gene expression and behavior. Genes Brain Behav 17:e12454
Briata, Paola; Bordo, Domenico; Puppo, Margherita et al. (2016) Diverse roles of the nucleic acid-binding protein KHSRP in cell differentiation and disease. Wiley Interdiscip Rev RNA 7:227-40
Gardiner, Amy S; Twiss, Jeffery L; Perrone-Bizzozero, Nora I (2015) Competing Interactions of RNA-Binding Proteins, MicroRNAs, and Their Targets Control Neuronal Development and Function. Biomolecules 5:2903-18
Sosanya, Natasha M; Cacheaux, Luisa P; Workman, Emily R et al. (2015) Mammalian Target of Rapamycin (mTOR) Tagging Promotes Dendritic Branch Variability through the Capture of Ca2+/Calmodulin-dependent Protein Kinase II ? (CaMKII?) mRNAs by the RNA-binding Protein HuD. J Biol Chem 290:16357-71
Wang, Feifei; Tidei, Joseph J; Polich, Eric D et al. (2015) Positive feedback between RNA-binding protein HuD and transcription factor SATB1 promotes neurogenesis. Proc Natl Acad Sci U S A 112:E4995-5004
Yoo, Soonmoon; Kim, Hak H; Kim, Paul et al. (2013) A HuD-ZBP1 ribonucleoprotein complex localizes GAP-43 mRNA into axons through its 3' untranslated region AU-rich regulatory element. J Neurochem 126:792-804
Bird, Clark W; Gardiner, Amy S; Bolognani, Federico et al. (2013) KSRP modulation of GAP-43 mRNA stability restricts axonal outgrowth in embryonic hippocampal neurons. PLoS One 8:e79255
Allen, Megan; Bird, Clark; Feng, Wei et al. (2013) HuD promotes BDNF expression in brain neurons via selective stabilization of the BDNF long 3'UTR mRNA. PLoS One 8:e55718
Perrone-Bizzozero, Nora; Bird, Clark W (2013) Role of HuD in nervous system function and pathology. Front Biosci (Schol Ed) 5:554-63
Sosanya, Natasha M; Huang, Peggy P C; Cacheaux, Luisa P et al. (2013) Degradation of high affinity HuD targets releases Kv1.1 mRNA from miR-129 repression by mTORC1. J Cell Biol 202:53-69

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