Postsynaptic roles of ankyrins

NIH RePORTER · NIH · R01 · $639,821 · view on reporter.nih.gov ↗

Abstract

ABSTRACT Extensive evidence implicates glutamatergic synapses as key pathogenic sites in neuropsychiatric disorders (NPDs). Recently-emerging evidence has implicated ankyrin proteins, including Ankyrin-G (AnkG), encoded by the ANK3 gene, and Ankyrin-B (AnkB), encoded by ANK2, in the biology of central nervous system synapses. While conventionally AnkG and –B have been seen as playing roles mainly at the axon initial segment, their functions in central glutamatergic synapses have only begun to be investigated, including in studies initiated by our laboratory. During the previous funding period, we have made extensive progress in understanding the regulation and interactome of AnkG at synapses and in dendrites. Our preliminary findings broaden our understanding of the neurobiology of ankyrins, and implicate them in several novel process, including deubiquitination and endocannabinoid signaling. In this proposal we will use neuroproteomics, conditional knockout and reporter mice, super-resolution and in vivo two-photon microscopy, calcium imaging, bioinformatics, and behavioral analyses, to investigate the functions of AnkG's protein partners in dendrite and at glutamatergic synapses. We hypothesize that AnkG performs multiple novel functions including supramolecular scaffold complex maintenance and regulation of endocannabinoid signaling, through which it controls spiny synapse development, structure, function, as well as circuit level network activity and behavior, in a cell type and developmental period-specific manner. We will test this hypothesis in the following Aims: Aim 1. To investigate the impact of cell type-dependent and developmentally-timed knock out of AnkG on brain structure, function, and behavior across maturation. Aim 2. To investigate the impact of cell type-dependent and developmentally-timed knock out of AnkB on brain structure, function, and behavior across maturation. Aim 3. To determine the mechanisms and functional significance of the interaction of AnkG with DAGLĮ. The proposed studies are highly novel and impactful, given that the synaptic functions of ankyrins are only beginning to be investigated. This proposal will be the first to investigate the function of several recently-discovered AnkG-interacting proteins in unexpected biological processes, using multiple cutting edge methods, and will open new avenues for many future studies.

Key facts

NIH application ID
10629210
Project number
5R01MH107182-07
Recipient
NORTHWESTERN UNIVERSITY
Principal Investigator
Peter Penzes
Activity code
R01
Funding institute
NIH
Fiscal year
2023
Award amount
$639,821
Award type
5
Project period
2015-03-01 → 2027-03-31