Scientists identify genetic variant that causes ALS

Wednesday, 25 January, 2023

Scientists identify genetic variant that causes ALS

Researchers at Nagoya University have identified a novel genetic variant found in some patients with amyotrophic lateral sclerosis (ALS). Employing human-induced pluripotent stem (iPS) cells, they detailed the process by which this variant relates to ALS. Their findings have been published in The Journal of Neuroscience.

ALS is a progressive and fatal neurodegenerative disease where a person gradually loses motor neurons and has muscle weakness. The mechanisms and causes of this disease are not well understood and there is no treatment. Furthermore, ALS is a diverse disease — different patients seem to have different causes, mechanisms and symptoms — although researchers do know that a protein called Fused in sarcoma (FUS) plays a key role in the disease. Ordinarily, FUS binds to RNA and regulates functions of RNA. On the other hand, FUS dysfunctions are associated with various neurodegenerative diseases, including ALS.

Dr Satoshi Yokoi and his colleagues at Nagoya University have been studying this FUS protein. Previously, they found that the FUS protein interacted with RNA that encodes a protein called SYNGAP1. SYNGAP1 helps with synaptic formation, which is essential for neurons to work together.

“Currently, no study has reported that SYNGAP1 is involved in the mechanism of ALS,” Yokoi said. “However, given its close relationship with FUS, we wanted to investigate whether SYNGAP1 has anything to do with ALS.”

First, the team searched for a variant of the SYNGAP1 gene in patients with ALS. They found seven out of 807 patients who had the variant. Next, to examine the behaviour of the SYNGAP1 variant, they replicated this variant gene in human iPS-derived motor neurons. An iPS cell is a type of stem cell that scientists can transform into any type of cell in the body, meaning researchers can generate, for example, diseased cells and conduct different tests on them in a living state.

The researchers generated motor neurons with the SYNGAP1 variant from iPS cells. In these neurons, researchers observed several abnormal behaviours compared to normal motor neurons; for example, the variant excessively recruited the FUS protein, as well as another RNA-binding protein called HNRNPK. This excessive binding inhibited synaptic formation. In particular, excessive recruitment of HNRNPK, rather than FUS, seemed to be a primary cause of synaptic dysfunction with the SYNGAP1 variant. Furthermore, when researchers applied antisense RNA that blocks the excessive binding of HNRNPK to SYNGAP1 RNA, they recovered synaptic formation, meaning that motor neurons can work together. This indicates that, in the future, scientists could utilise antisense RNA to develop ALS drugs.

Excessive binding of HNRNPK to SYNGAP1 was causing synaptic abnormality, which explains the process of early-stage ALS when synapse loss takes place. Additionally, while previous ALS research focused on FUS, this study underscored the crucial roles of SYNGAP1 and HNRNPK. The antisense RNA used in the current research is only effective for those patients with the variant SYNGAP1. Nonetheless, the researchers hope that the discovery of this new mechanism can provide new insight into other types of ALS.

The study also found that SYNGAP1 behaved differently in human iPS cells compared to the mouse model, which had been used for SYNGAP1 research. Yokoi said, “We believe that using human-derived samples is crucial so that the observations from these cells directly apply to patients.”

Although the researchers described one mechanism of ALS, much remains to be investigated because ALS involves multiple different mechanisms and causes. Yokoi said, “We will continue research to find something that can apply to future ALS treatments.”

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