Molecular overreaction to ribosome stalling leads to cognitive disorders, finds study
The link between quality control during protein synthesis in cells and neurological disorders has been made clear for the first time by RIKEN researchers. This discovery could help to develop new treatments for such cognitive disorders.
When this happens, an important quality-control process kicks in and degrades the incomplete protein threads that have been made, which would otherwise damage cells. This mop-up operation is known as ribosome-associated quality control (RQC).
Recently, there has been some evidence suggesting that various brain disorders result when RQC goes awry, but no-one knew how this occurs.
"Previous studies had suggested that dysfunction of RQC may lead to neurodegenerative disorders," says Motomasa Tanaka of the RIKEN Center for Brain Science. "So we are really interested in what happens in neurons, but most studies so far have focused on cultured cell lines or yeast cells rather than neurons."
Now, Ryo Endo, Tanaka and co-workers have discovered that removing a key gene in RQC in mice neurons leads to developmental defects in neurons. The study is published in the journal Proceedings of the National Academy of Sciences.
Specifically, the team found that mice lacking an enzyme known as LTN1 had higher levels of two signaling molecules: TTC3 and UFMylation. "The abundance of the protein TTC3 increased more than tenfold," notes Tanaka. "That was really surprising as it's an overkill."
These signaling molecules serve to turn off the translation of genetic material into proteins—a beneficial effect. But they go too far and apply the brakes to the growth of neurites—projections from neurons that go on to form connections with other neurons. It is this inhibition of neurites that is thought to lead to problems in neurons.
"Overexpression of TTC3 definitely helps to stop translation, which is a good thing," says Tanaka. "But at the same time it also curbs neurite extension, reducing communication between neurons. This is probably the cause of cognitive dysfunction."
Tanaka likes this creation of a more dire situation due to overcompensating for the initial problem of an overactive immune system that can cause serious conditions such as chronic inflammation and allergies.
The finding could help to develop new therapies. "We think some therapeutic strategies to target TTC3 or illumination signaling factors may also be interesting in the future," says Tanaka.
The team now intends to explore the relationship between the accumulation of signaling dysfunction and human brain disorders.
More information: Ryo Endo et al, Dysregulation of ribosome-associated quality control elicits cognitive disorders via overaccumulation of TTC3, Proceedings of the National Academy of Sciences (2023). DOI: 10.1073/pnas.2211522120