Person

Beattie, Christine (Deceased)

Person ID
ZDB-PERS-960805-47
Email
beattie.24@osu.edu, Christine.Beattie@osumc.edu
URL
http://u.osu.edu/zebrafish
Affiliation
Beattie Lab
Address
The Center for Molecular Neurobiology Department of Neuroscience The Ohio State University 190 Rightmire Hall 1060 Carmack Road Columbus, OH 43210 USA
Country
United States
Phone
(614) 292-5113
Fax
(614) 292-5379
ORCID ID
Biography and Research Interest
   Our goal is to understand motoneuron development and function in the context of motoneuron diseases. We focus on two diseases, spinal muscular atrophy (SMA), an infant/childhood onset motoneuron disease and amyotrophic lateral sclerosis (ALS) and adult onset disease. We use zebrafish as a vertebrate model organism due to its well characterized nervous system and its relatively simple neuromuscular organization. We have generated genetic models of these diseases in zebrafish and are applying genetics, cell biology and electrophysiology to understand differences between wild-type motoneurons and motoneurons in these disease models.

SMA is an infant/childhood onset motoneuron disease. We have found that when the protein linked to this disease, survival motor neuron protein (SMN), is decreased motoneurons exhibit aberrant axonal development, decreased axonal actin dynamics, and decreased dendrites. Our goal now is to identify why this is and what genes downstream of SMN are involved. This will lend insight into the normal processes of motoneuron development and the function of this disease gene in the process.

ALS is an adult onset disease. However, we are very interested in understanding the earliest changes that occur in motoneurons in this disease. Our hypothesis is that changes occur early in the spinal cord and that over time these changes damage the cell to the point where it cannot function. We will test this hypothesis using a combination of electrophysiology, RNA expression analysis and in vivo calcium imaging. Knowledge of these early changes will not only define a mechanism of toxicity but will reveal in vivo biomarkers. In future work, these biomarkers can be used to design high throughput screens in zebrafish larvae to aid in drug development and testing.
Publications
Non-Zebrafish Publications