Two new studies have recently been published that suggest we’re closer to understanding the genetic makeup of autism, a neurodevelopmental childhood disorder that affects approximately 1 in 150 children in the U.S.
One study pinpoints a gene region that may account for as many as 15 percent of autism cases. The second study identifies missing or duplicated stretches of DNA along two crucial gene pathways.
Significantly, both studies detected genes implicated in the development of brain circuitry in early childhood.
“Because other autism researchers have made intriguing suggestions that autism arises from abnormal connections among brain cells during early development, it is very compelling to find evidence that mutations in genes involved in brain interconnections increase a child’s risk of autism,” said study leader Hakon Hakonarson, M.D., Ph.D., director of the Center for Applied Genomics at The Children’s Hospital of Philadelphia.
Autism is the best known of the autism spectrum disorders (ASDs), a group of childhood neurodevelopmental disorders that cause impairments in verbal communication, social interaction and behavior.
Previous studies have implicated several chromosome regions harboring rare variants in raising the risk of autism spectrum disorders, but until now, research has not been consistent in identifying and replicating common genetic variants.
One of the two studies by Hakonarson’s team is the first to identify common genetic variants associated with autism. By using highly automated genotyping tools that scan the entire genome of thousands of individuals, the researchers found that children with ASDs were more likely than healthy controls to have gene variants on a particular region of chromosome 5. That region is located between two genes, cadherin 9 (CDH9) and cadherin 10 (CDH10), which carry codes to produce neuronal cell-adhesion molecules.
Neuronal cell-adhesion molecules are important because they affect how nerve cells communicate with each other, thought to be an underlying problem in ASDs. “These molecules are expressed on the cell surfaces of neurons, and they are involved with shaping both the physical structure of the developing brain and the functional connections among different brain regions,” Hakonarson said. “Although a particular gene variant may contribute a small risk for an ASD in a particular individual, we estimate that the variants we discovered may contribute to as many as 15 percent of ASD cases in a populationâ€”typically referred to as the population-attributed risk of the variant.”
Hakonarson’s team first performed genome-wide association studies on DNA from over 3,100 subjects from 780 families of children affected with ASDs, then performed further studies in a cohort of 1,200 affected subjects and 6,500 unaffected controls. They then replicated their results in two additional independent cohorts. In total, they analyzed DNA from 12,834 subjects.
Hakonarson’s second study identified copy number variations — deletions or duplications of DNA — that increase a child’s risk of having an autism spectrum disorder. Interestingly, these variants were enriched in genes that belong to two biological pathways, one including the same neuronal cell-adhesion molecule gene family that harbored the common variant reported in Hakonarson’s first study. The other gene cluster impacted by copy number variations belongs to the ubiquitin degradation pathway. Ubiquitins are a class of enzymes that eliminate connections among nerve cells, and are involved with processing and degrading neuronal cell-adhesion moleculesâ€”thus linking the two gene pathways together.
“The copy number variations we discovered are active on two gene networks that play critical roles in the development of neuronal connectivity within the central nervous system,” said Hakonarson. “Finding genes that are biologically relevant to these neuronal systems increases our understanding of how autism originates.”
The gene discoveries, added Hakonarson, converge with evidence from functional magnetic resonance imaging that children with ASDs may have reduced connectivity among neural cells, and with anatomy studies that have found abnormal development of the brain’s frontal lobes in patients with autism.
“Many of the genes we identified concentrate their effects in brain regions that develop abnormally in autistic children,” said Hakonarson. “Our current findings, when coupled with anatomical and imaging studies, may suggest that ASDs are a problem of neuronal disconnection.”
His group’s ongoing research, continued Hakonarson, focuses on investigating the exact mechanisms by which these genetic variations cause autistic disorders. “For instance, we expect to manipulate similar cell-adhesion genes in mice to see if the animals show altered social behaviors that may correspond to human behaviors.” In addition, other genes remain to be discovered.
“Although we cannot immediately apply this research to clinical treatments, these findings increase our understanding of how autism spectrum disorders arise, and may in time foster the development of strategies for prevention and early treatment,” said developmental pediatrician Susan E. Levy, M.D., a co-author of both studies who is the medical director of the Regional Autism Center and a member of the Center for Autism Research (CAR), both at Children’s Hospital.
Collaborating with researchers from more than a dozen institutions, including members of the Autism Genome Project (AGP), the studies appeared in the April 28 online publication of the journal, Nature.
Source: The Children’s Hospital of Philadelphia