Autism-Related Mutations Inhibit Export of Key Protein From Endoplasmic Reticulum – Neuroscience News
Summary: Study finds an autism-related genetic mutation increases splicing errors and induces endoplasmic reticulum stress by activating the unfolded protein response.
Source: University of Tsukuba
Anyone who has ever gotten stuck in a traffic jam can attest to the disruption that it causes to your day. Now, researchers from Japan have found that an autism-associated mutation can cause a traffic jam of unfolded proteins that disrupts normal brain function.
In a study that was recently published in Scientific Reports, researchers from the University of Tsukuba reveal that a mutation in an autism-associated protein called Hevin impairs its normal processing and secretion.
Many gene mutations associated with autism spectrum disorder have been identified to date, including some mutations that are inherited. However, in most cases the functional effects of these mutations have not been determined.
“We previously found that mutation of the Usp15 gene, which is closely associated with autism, increases the probability of splicing errors and induces endoplasmic reticulum stress by activating the unfolded protein response,” explains Professor Fuminori Tsuruta. “However, it remained unclear how it causes these effects.”
To address this, the researchers looked for autism-associated variants that exhibited abnormal splicing in the absence of Usp15 in mouse brains and found that the tail end of the transcript encoding a protein called Hevin tends to be lacking. Intriguingly, a mutation in the same part of Hevin, known as the EF-hand motif, has been associated with a familial case of autism.
“Analysis of the Hevin deletion mutant and the Hevin variant with a single point mutation showed that both mutants accumulated in the endoplasmic reticulum, leading to activation of the unfolded protein response,” says Professor Tsuruta.
Importantly, structural modeling of the Hevin mutation associated with familial autism showed that this single amino acid substitution triggers exposure of a hydrophobic amino acid to the surface. This change is likely to cause structural instability and interfere with export from the endoplasmic reticulum.
“Taken together, our findings suggest that the integrity of the EF-hand motif in Hevin is crucial for proper folding, and that autism-related mutations impair the export of Hevin from the endoplasmic reticulum,” says Professor Tsuruta.
Given that several other autism-related mutations have also been shown to promote the accumulation of synaptic proteins in the endoplasmic reticulum, it is possible that the resulting impairment in neuronal function contributes to autism pathogenesis.
Future studies may help reveal how the endoplasmic reticulum stress response affects neural circuits and brain homeostasis and clarify the link to autism development.
About this genetics and autism research news
Author: Press Office
Source: University of Tsukuba
Contact: Press Office – University of Tsukuba
Image: The image is in the public domain
Original Research: Open access.
“Autism-associated mutation in Hevin/Sparcl1 induces endoplasmic reticulum stress through structural instability” by Takumi Taketomi et al. Scientific Reports
Autism-associated mutation in Hevin/Sparcl1 induces endoplasmic reticulum stress through structural instability
Hevin is a secreted extracellular matrix protein that is encoded by the SPARCL1 gene. Recent studies have shown that Hevin plays an important role in regulating synaptogenesis and synaptic plasticity. Mutations in the SPARCL1 gene increase the risk of autism spectrum disorder (ASD).
However, the molecular basis of how mutations in SPARCL1 increase the risk of ASD is not been fully understood. In this study, we show that one of the SPARCL1 mutations associated with ASD impairs normal Hevin secretion.
We identified Hevin mutants lacking the EF-hand motif through analyzing ASD-related mice with vulnerable spliceosome functions. Hevin deletion mutants accumulate in the endoplasmic reticulum (ER), leading to the activation of unfolded protein responses.
We also found that a single amino acid substitution of Trp647 with Arg in the EF-hand motif associated with a familial case of ASD causes a similar phenotype in the EF-hand deletion mutant. Importantly, molecular dynamics (MD) simulation revealed that this single amino acid substitution triggers exposure of a hydrophobic amino acid to the surface, increasing the binding of Hevin with molecular chaperons, BIP.
Taken together, these data suggest that the integrity of the EF-hand motif in Hevin is crucial for proper folding and that ASD-related mutations impair the export of Hevin from the ER.
Our data provide a novel mechanism linking a point mutation in the SPARCL1 gene to the molecular and cellular characteristics involved in ASD.
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