Scientists in a recent study have explained how damage to RNA-binding protein known as hnRNP A2/B1 contributes to amyotropic lateral sclerosis by scrambling crucial cellular messaging systems. The findings of the study published in Neuron.
"Our findings are a significant step forward in validating RNA-based therapy as a treatment for ALS," said senior author Gene Yeo, PhD, professor of cellular and molecular medicine at UC San Diego School of Medicine.
‘RNA based therapy as a treatment for amyotrophic lateral sclerosis (ALS)’
ALS, also known as Lou Gehrig's disease, is a devastating neurological condition affecting more than 20,000 Americans. The disease greatly diminishes patients' quality of life and is terminal. ALS affects a special kind of nerve cell called a motor neuron. These motor neurons enable us to move our bodies. Currently, there are no effective treatments for ALS, largely due to poor understanding of how the disease initiates and progresses at the molecular level.
Yeo's team studies RNA-binding proteins and their ability to control how, when and if cells make certain proteins. To unravel the role RNA-binding proteins play in ALS, Yeo's team gathered skin cells from four patients with the disease — three with mutations in the hnRNP A2/B1 gene, one with a mutation in a different gene — and two healthy volunteers as controls. The researchers coaxed these skin cells into becoming a special kind of stem cell called induced pluripotent stem cells (iPSCs) and ultimately turned these patient-specific stem cells into motor neurons. This technique provided them with personalized models of each patient's disease, in a laboratory dish, where it's easy to do experiments.
To determine the effects of the mutant hnRNP A2/B1 proteins in these samples, the researchers then measured the activity of thousands of genes in each of the ALS and healthy motor neuron samples. In the ALS patient samples, Yeo and team found that the hnRNP A2/B1 mutation these patients had didn't merely disable the protein. Instead, the mutation gave the protein new toxic properties that scrambled RNA processing, and ultimately led to the death of motor neurons.
Yeo said these findings may have important implications for their collaborators and others who are developing therapeutics that aim to treat disease by targeting RNA.
"These RNA-targeting therapies can eliminate toxic proteins and treat disease," said first author Fernando Martinez, a graduate student in Yeo's laboratory. "But this strategy is only viable if the proteins have gained new toxic functions through mutation, as we found here for hnRNP A2/B1 in these ALS cases."
Environmental factors are thought to contribute to ALS, increasing the chances a person with a genetic predisposition will get the disease. To mimic this scenario, Martinez compared how motor neurons from ALS patients and healthy individuals respond to stress. In the patient-specific ALS motor neurons under stress, they found more hnRNP A2/B1 proteins clumped in a part of the cells called stress granules, as compared to healthy cells.
"Drugs that lower the exaggerated reaction to stressors that we saw in motor neurons from ALS patients may also prove a powerful therapeutic strategy," Yeo said. "It is likely that multiple, multi-directional shots at goal will be needed to treat this debilitating disease."
Study co-authors also include: Gabriel A. Pratt, Eric L. Van Nostrand, Ranjan Batra, Stephanie C. Huelga, Chelsea Gelboin-Burkhart, Layla Fijany, Harrison Wang, Julia K. Nussbacher, Balaji Sundararaman, Rea Lardelli, Jens Lykke-Andersen, UC San Diego; Katannya Kapeli, UC San Diego and National University of Singapore; Peter Freese, Christopher B. Burge, MIT; Seung J. Chun, Karen Ling, Frank Bennett, Frank Rigo, Ionis Pharmaceuticals; Sara M. Broski, Ashkan Javaherian, Gladstone Institute of Neurological Disease; Hong Joo Kim, J. Paul Taylor, Howard Hughes Medical Institute and St. Jude Children's Research Hospital; John P. Donohue, Manuel Ares Jr., UC Santa Cruz; and Steven Finkbeiner, Gladstone Institute of Neurological Disease and UC San Francisco.
This research was funded, in part, by the National Institutes of Health (HG004659, NS075449, U54HG007005, T32GM008666, T32CA067754), CIRM (RB3-05009, RB4-06045), ALS Association (VC8K27), Alfred P. Sloan Foundation (fellowship BR2011-023) and National Science Foundation Graduate Research Fellowships (DGE-0707423, DGE-1144086, DGE-1144086, DGE-1650112).