A variation of a gene linked to autism influences how neurons connect and communicate with each other in the brain, according to a study from Washington University School of Medicine in St. Louis. Mice that lack the gene form too many connections between neurons and have learning problems.
The findings suggest that some of the diverse characteristics of autism may be caused by a malfunction in communication among cells in the brain.
“This study raises the possibility that there may be too many synapses in the brains of patients with autism. You might think that having more synapses would make the brain work better, but that doesn’t seem to be the case. An increased number of synapses creates miscommunication among neurons in the developing brain that correlates with impairments in learning, although we don’t know how,”
said senior author Azad Bonni, MD, PhD, the Edison Professor of Neuroscience and head of the Department of Neuroscience at Washington University School of Medicine in St. Louis.
Autism is a neurodevelopmental disorder affecting about one out of every 68 children. It is characterized by social and communication challenges.
Among the many genes linked to autism in people are six genes that attach a molecular tag, called ubiquitin, to proteins. These genes, called ubiquitin ligases, function like a work order, telling the rest of the cell how to deal with the tagged proteins: this one should be discarded, that one should be rerouted to another part of the cell, a third needs to have its activity dialed up or down.
Individuals with autism spectrum disorders may carry a gene mutation that prevents one of their ubiquitin genes from working properly. But how problems with tagging proteins affect how the brain is hardwired and operates, and why such problems may lead to autism, has remained poorly understood.
RNF8 operates in the cytoplasm to suppress presynaptic differentiation in vivo. a) Immunoblotting analyses of fractionated lysates of P8 rat cerebellum revealed abundant endogenous RNF8 in the cytoplasmic fraction in the cerebellum. b) P4 rat pups were electroporated with an expression plasmid encoding an RNF8–GFP fusion protein together with a mCherry expression plasmid. After 8 days, rat pups were sacrificed and the cerebellum was subjected to immunohistochemistry using GFP and DsRed (mCherry) antibodies. RNF8 localizes predominantly in the cytoplasm. c) P4 rat pups were electroporated with the control U6 plasmid or RNF8 RNAi plasmid together with an expression plasmid encoding NES(nuclear export signal)-RNF8Res fusion protein, NLS(nuclear localization signal)-RNF8Res fusion protein or the control vector and with the GFP expression plasmid. Expression of NES-RNF8Res, but not NLS-RNF8Res, reversed the RNF8 RNAi-induced phenotype of increased number of parallel fiber presynaptic boutons in the cerebellum in vivo (*p < 0.05, ANOVA followed by Fisher’s PLSD post hoc test, n = 3–4 rats). Scale bars = 10 μm Credit: Pamela Valnegri, et al. CC-BY
To understand the role of ubiquitin genes in brain development, Bonni, first author Pamela Valnegri, PhD, and colleagues removed the ubiquitin gene RNF8 in neurons in the cerebellum of young mice.
The researchers found that neurons that lacked the RNF8 protein formed about 50 percent more synapses – the connections that allow neurons to send signals from one to another – than those with the gene. And the extra synapses worked.
By measuring the electrical signal in the receiving cells, the researchers found that the strength of the signal was doubled in the mice that lacked the protein.
RNF8 Gene Knock-out
The cerebellum is indispensable for movement and learning motor skills such as how to ride a bicycle. Some of the recognizable symptoms of autism – such as motor incoordination and a tendency to walk tippy-toed – involve control of movement.
The animals missing the RNF8 gene in the neurons of their cerebellum did not have any obvious problems with movement: they walked normally and appeared coordinated. When the researchers tested their ability to learn motor skills, however, the mice without RNF8 failed miserably.
The researchers trained the mice to associate a quick puff of air to the eye with the blinking of a light. Most mice learn to shut their eyes when they see the light blink, to avoid the irritation of the coming air puff.
Cerebellar-dependent learning is impaired in RNF8 or UBC13 conditional knockout mice. a) Schematic of delayed eye-blink conditioning assay depicting a mouse trained with a conditioned stimulus (CS: blue LED) paired with an eyeblink-eliciting unconditioned stimulus (US: periocular air puff). Depletion of RNF8 (b) or UBC13 (c) impaired performance on the eye-blink conditioning task (***p < 0.005, *p < 0.05, ANOVA followed by Fisher’s PLSD post hoc test) Credit: Pamela Valnegri, et al. CC-BY
After a week of training, mice with a functioning copy of the gene closed their eyes in anticipation more than three quarters of the time, while mice without the gene shut their eyes just a third of the time.
Too Many Synapses
While it is best known for its role in movement, the cerebellum is also important in higher cognitive functions such as language and attention, both of which are affected in autism. People with autism often have language delays and pay unusually intense attention to objects or topics that interest them.
The cerebellum may be involved not only in motor learning but in other features of autism as well, the researchers said.
Of course, there is a world of difference between a mouse that can’t learn to shut its eyes and a person with autism who struggles to communicate. But the researchers said the findings suggest that changing how many connections neurons make with each other can have important implications for behaviour.
Since this paper was written, Bonni and colleagues have tested the other autism-associated ubiquitin genes. Inhibition of all genes tested cause an increase in the number of synapses in the cerebellum.
“It’s possible that excessive connections between neurons contribute to autism. More work needs to be done to verify this hypothesis in people, but if that turns out to be true, then you can start looking at ways of controlling the number of synapses. It could potentially benefit not just people who have these rare mutations in ubiquitin genes but other patients with autism,”
The work was supported by the NIH, the Mathers Foundation, and the European Molecular Biology Organization.