# Uncovering the transcriptional regulatory roles of ataxin-2 in neuronal function and neurodegenerative disease

> **NIH NIH F31** · UNIVERSITY OF CALIFORNIA, SAN DIEGO · 2020 · $39,247

## Abstract

ABSTRACT
Ataxin-2 (ATXN2) is a ubiquitously expressed RNA-binding protein (RBP) conserved across eukaryotic species
from yeast to human. Trinucleotide (CAG) repeat expansion mutations of the poly-glutamine (polyQ) tract of the
ATXN2 gene are associated with several neurodegenerative diseases including spinocerebellar ataxia 2 (SCA2)
and amyotrophic lateral sclerosis (ALS), a fatal adult-onset disorder characterized by the progressive death of
motor neurons of the brain and spinal cord. In vivo models recapitulate this link to motor neuron degeneration
and ALS, as ataxin-2 is reported to be a toxic modifier of TDP-43, a protein most commonly associated with both
the familial and sporadic forms of ALS. Studies have supported this toxic gain-of-function model, as reduction of
ataxin-2 levels seems to serve a protective role against neuron degeneration while simultaneously prolonging
survival in Atxn2-null mice in the presence of TDP-43 overexpression. At the same time, endogenous neural-
specific functions of ataxin-2 are still poorly understood, as are its direct role in mediating ALS pathogenesis.
This project aims to uncover the transcriptome-wide regulatory role of ataxin-2 in the central nervous system in
order to mechanistically characterize the interaction between ATXN2 mutations and motor neuron death. This
proposal seeks to use molecular and genomic techniques, including eCLIP-seq, RNA-seq and ribosome profiling,
to map the physical and functional “interactome” of ataxin-2 in mouse brain and spinal cord, as well as in human
iPSC-differentiated motor neurons. To address the connection to motor neuron disease, this proposal also aims
to generate an isogenic iPSC model using CRISPR/Cas9 technologies by knocking-in ALS-associated polyQ
expansion sequences into the ATXN2 genomic locus. These cell lines will then be differentiated into mature
motor neurons in order to study neural-specific transcriptional and translational perturbations introduced through
repeat expansions. This study will directly characterize the role of ataxin-2 in neuron-specific RNA metabolism,
as well as identify specific target genes disrupted with polyQ mutations. If successful this research will define the
underlying molecular mechanisms linking ataxin-2 to ALS risk, identify novel disease-relevant pathways that
potentially serve as targetable avenues for therapy, and provide a broadly applicable disease modeling strategy
to investigate the direct genetic influence of other repeat expansion mutations in future work.

## Key facts

- **NIH application ID:** 10051331
- **Project number:** 5F31NS111859-02
- **Recipient organization:** UNIVERSITY OF CALIFORNIA, SAN DIEGO
- **Principal Investigator:** Ryan J Marina
- **Activity code:** F31 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $39,247
- **Award type:** 5
- **Project period:** 2019-09-02 → 2021-09-01

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10051331

## Citation

> US National Institutes of Health, RePORTER application 10051331, Uncovering the transcriptional regulatory roles of ataxin-2 in neuronal function and neurodegenerative disease (5F31NS111859-02). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10051331. Licensed CC0.

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