From extending lifespan to bolstering the immune system, the drug’s effects are only just beginning to be understood.
As researchers sequence the DNA of thousands of kids with autism, dozens of genetic subgroups are emerging.
August 1, 2016|
In late 2013, psychologist Raphael Bernier welcomed a 12-year-old girl and her parents into his office at the University of Washington (UW) in Seattle. The girl had been diagnosed with autism spectrum disorder, and Bernier had invited the family in to discuss the results of a genetic analysis his collaborator, geneticist Evan Eichler, had performed in search of the cause.
As they chatted, Bernier noticed the girl’s wide-set eyes, which had a slight downward slant. Her head was unusually large, featuring a prominent forehead. The mother described how her daughter had gastrointestinal issues and sometimes wouldn’t sleep for two to three days at a time. The girl’s presentation was interesting, Bernier recalls, but he didn’t think too much of it—until a week later, when he met an eight-year-old boy with similarly wide-set eyes and a large head.
Bernier did a double take. The “kiddos,” as he calls children who come to see him, could have been siblings. According to the boy’s parents, he also suffered from gastrointestinal and sleep problems. The similarities between the unrelated children were remarkable, especially for a disorder so notoriously complex that it has been said, “If you’ve met one child with autism, you’ve met one child with autism.” But Bernier knew that the patients shared another similarity that might explain the apparent coincidence: both harbored a mutation in a gene known as chromodomain helicase DNA binding protein 8 (CHD8).
CHD8 produces a protein that regulates chromatin—the conglomeration of tightly packed DNA and proteins in the nucleus—during fetal development. A year earlier, Bernier and Eichler had screened the genomes of 2,000 children for mutations in genes suspected to be involved in autism. Nine of those 2,000 had disruptive mutations in CHD8, and Bernier had now met two of them.
Bernier began inviting others with CHD8 mutations from around the world to his lab. To date, he has met or reviewed records from 25 such children. They all present with similar physical appearances and symptoms.1 Mutated CHD8 is now one of dozens of recognized genetic subtypes of autism. Bernier suspects there are many more.
It’s cancer all over again. The victories we’ve had over cancer weren’t for the disease in its entirety, but gradually picking apart subtypes of the disease and developing therapies for those.—Evan Eichler,
University of Washington
A large proportion of autism research begins with and is centered upon external presentations of the disorder, primarily behavioral manifestations such as social communication difficulties and repetitive behaviors. Such measures are crude, however, and symptoms often present in different combinations. To better define the disorder, Bernier, Eichler, and others are instead looking for molecular, cellular, and anatomical indicators of autism, including single genetic mutations as well as the behavior of 10-week-old neurons cultured from patients’ skin cells and the folding of brain tissue in two-year-old children.
This inside-out approach has confirmed a long-held suspicion that autism is not a single biological disorder. The causes and types of autism are as multitudinous as the symptoms, and any successful treatments will likely be as varied. “It’s cancer all over again,” says Eichler. “The victories we’ve had over cancer weren’t for the disease in its entirety, but gradually picking apart subtypes of the disease and developing therapies for those.”
CELL, 158:263–76, 2014When Bernier joined the UW faculty in 2008, the vast majority of autism cases were considered “idiopathic,” of unknown origins. Despite the fact that autism is a highly heritable disease, no smoking gun had been found in the genome. The prevailing theory was that autism is caused by unfortunate combinations of common mutations.
Eichler, a geneticist who joined UW in 2004, did not subscribe to that theory. In 2006, his lab was in the midst of publishing a dozen papers linking copy number variations (CNV)—large deletions or duplications in the genome—to neurodevelopmental disorders, including about 7 percent to 8 percent of autism cases. Eichler and his colleagues found that patients with particular CNVs often presented with similar phenotypes. “We didn’t set out to do this, but we started to define new syndromes,” which are referred to by CNV position, such as 17q21 (on the long arm of chromosome 17), says Eichler.
At the time, it was prohibitively expensive to look for mutations at the level of individual genes. But that was about to change. Just as next-generation sequencing was coming onto the scene, Eichler met Bernier, who was studying neural mechanisms underlying autism. In 2008, at an all-day UW meeting, the chair of genome sciences suggested Bernier reach out to Eichler. “He said, ‘I bet you’ll get along well,’” Bernier recalls.
That was an understatement. “It was love at first sight,” says Eichler with a laugh. Now close friends, they embarked on a joint research endeavor to identify genotypes associated with autism. The majority of past studies—and many current ones—began with a rigorous phenotyping of a child with the disorder, followed by a genetic analysis. Eichler, after his experience with CNVs, opted to put genetics first and foremost. For each subject, he began with a deep dive into the genome.
Eichler’s team performed exome sequencing on 677 DNA samples from 209 families who had donated blood to the Simons Simplex Collection, where each family has one child with autism. Most of the mutations he identified were spontaneous—not found in either parent—and they disrupted the function of proteins in similar biological pathways, such as synapse function or chromatin remodeling.2 But hundreds of different genes were affected, meaning few children had any mutated genes in common.
The researchers then performed targeted sequencing on 44 candidate genes in 2,446 children with autism. This time, thanks to the larger pool of participants, the scientists began to identify clusters of children with the same mutated genes. For example, disruptive mutations in any of six genes—CHD8, DYRK1A, GRIN2B, TBR1, PTEN, and TBL1XR1—appeared to be responsible for 1 percent of sporadic cases of autism.3
Bernier began inviting these children to his lab for two to three days of phenotyping, from brain scans to cognitive tests. When combined with genetic screens of idiopathic autism patients from collaborating physicians around the world, defined subgroups began to emerge. For example, children with mutations in DYRK1A have unusually small heads and skull deformities, in addition to behavioral traits characteristic of autism. Individuals with a 16p11.2 deletion are engaged but socially awkward, and have high rates of psychiatric disorders.4 And CHD8 mutations, as Bernier had noticed, are linked with wide-set eyes, large heads, and sleep and gastrointestinal problems. To study CHD8 further, Eichler worked with geneticists at Duke University to create a zebrafish model that carried a mutated version of the gene; the fish developed large heads and poor GI function.
Bernier and Eichler are currently three years into a grant from the National Institutes of Health to track down and fly in individuals from around the world to compare phenotypes to genetic profiles and continue to identify such subtypes. In 2011, the two estimated that more than 800 genes are involved in autism. Today, there are about 100 that have been confidently linked to the disorder, says Eichler, and another several hundred have been flagged as candidates. In 2014, the team collaborated with two other labs—led by Michael Wigler at Cold Spring Harbor Laboratory and Matthew State, then at Yale—to determine that about 30 percent of “idiopathic” cases appear to be due to a large CNV deletion or duplication or a known, spontaneous genetic mutation in a protein-coding gene.5 Wigler suspects that another 20 percent of such cases are attributable to mutations carried by unaffected mothers—who are protected by as-yet-unexplained factors—that cause autism in their sons.6
Once a few treatments are discovered, autism research will once again follow in the footsteps of cancer research, where a drug approved for one cancer type subsequently proved beneficial in others.
Wigler has spent the last five years studying spontaneous, rare mutations that may play causal roles in autism, and recently narrowed a list of genetic suspects to a proposed set of 200 “vulnerable” genes, as he calls them. He found these vulnerable genes have fewer mutations than typical human genes, suggesting the genes are protected by evolution due to adaptive disadvantages when they are mutated.7 A surprising proportion of them are expressed in the developing brain in utero but then sharply reduced in expression after birth. Many of the genes, like CHD8, affect chromatin structure, while others code for proteins involved in receptor-signaling pathways.
“There’s no sore thumb in the group,” says Wigler. “I would say, by and large, the brain has a set of genes that are critical for its highest level of development, and some of those genes are [required] to have a healthy brain.”
Functional studies are ongoing, and there are many other autism-linked genotypes yet to be discovered, but already the work is having a “magical” impact on families, says Eichler. “Once these families are linked by a common genetic etiology, they become a little society of themselves, sharing practical life experiences and how to cope with their kids’ disabilities.”
© ISTOCK.COM/MATHISWORKS/NEYRO2008Of course, not all forms of autism appear to be caused by genetic abnormalities. Even the most hard-core geneticists in the field—Eichler, Bernier, and Wigler included—are quick to note that genetics does not and will not explain every autism case. Numerous nongenetic factors, such as environmental conditions, can affect the developing brain. For example, premature infants who experience a brain bleed have a 30-fold higher incidence of autism than the general population. To identify other contributors to autism, researchers are working toward a better understanding of neural development. And thanks to advances in induced pluripotent stem cell (iPSC) technology, scientists can now grow entire brain-like structures (organoids) derived from cells of patients with autism.
Last year, Yale University’s Flora Vaccarino and colleagues reprogrammed skin cells from boys with autism who also had large heads—a condition known as macrocephaly, a relatively common phenotype in autism patients—into iPSCs, then differentiated the cells into neurons. Under special culturing conditions, the cells developed into 3-D organoids—mini brains—that mimic forebrain development at about 10 to 16 weeks post-conception, says Vaccarino. The researchers also created organoids using the cells of the boys’ healthy fathers, and compared them to those structures derived from the boys’ cells. (See “Mini Brains Model Autism,” The Scientist, July 16, 2015.)
Vaccarino initially expected to study dozens of families before finding statistically significant results. But after just four father-son pairs, she had found that the boys’ cells grew significantly faster than their fathers’ cells, and that they overexpressed genes involved in brain cell proliferation, inhibitory neuron fate, and synapse assembly.8 These differences are likely not a result of macrocephaly, Vaccarino notes, as the fathers had large heads as well, and because the differences were directly correlated to the behavioral symptoms of the children. Vaccarino suggests that the neurological differences might thus be causally related to autism, but she cautions that more families are needed to draw definitive conclusions. Her team also plans to study cells from patients with autism and normal head sizes.
At the level of the whole organ, researchers have revealed a biological indicator of autism buried in the deepest folds of the brain. Researchers used to believe cortical folds in the brain are set before birth, but Christine Deruelle at the Institut de Neurosciences de la Timone in Marseille, France, and colleagues recently used MRI imaging to show that sulcal pits—the deepest part of each fold of the cerebral cortex—continue to deepen after birth, and that the number of sulcal pits increases when a child is about 2 years old, a common age of onset for autism. Comparing the brains of boys with autism, aged 2 to 10, with boys suffering from a development disorder or typically developing boys, the researchers found that certain sulcal pits were shallower among children with autism. In a small region of the brain involved in language and communication called Broca’s area, the sulcal pits in the autism patients appeared to be wasting away—although, paradoxically, the deeper the pit, the more impaired a child’s social communications skills were.9 “It’s like the maturation of this small part of the brain was disrupted,” says Deruelle.
Such retrospective studies cannot distinguish between causes and consequences of the disorder. Yet a prospective study that begins following children before they develop symptoms would require a prohibitively large number of participants to ensure that a sizable quantity of autism patients are enrolled, considering that only 1 in 45 to 68 children in the U.S. develops the disorder each year. That is, unless a scientist studies a population of children at higher risk for autism.
|WHAT'S IN A GENE?|
Many of the genes involved in autism affect chromatin structure, while others produce proteins involved in receptor-signaling pathways, synapse development,
axon targeting, and neuron motility.
|Functional category||Exemplar genes|
|Chromatin structure||CHD8, TBL1XR1|
|Signaling pathways||DYRK1A, SCN2A, PTEN, CTNND2, GRIN2B|
|Synapse development||RAS, SHANK2/3, RhoA/B, MAPK3, SynGAP1|
|Axon targeting||TBR1, NRXN1, NLGN3|
|Actin network||MYH11, FLNA, CYFIP1|
|Neuron motility||DCC, WNT|
Mustafa Sahin, a neurologist at Harvard Medical School and Boston Children’s Hospital, works with children suffering from a rare genetic disorder called tuberous sclerosis (TSC), characterized by the growth of benign tumors in the brain and other vital organs. Over the years, Sahin has found that about 50 percent of children with TSC develop autism. And because TSC is typically diagnosed in utero or as an early newborn, these kids constitute a population that researchers could follow to study the onset of autism, Sahin reasoned.
In an initial brain imaging study in 2013, his team found that the children with TSC who develop autism have less connectivity, and less-organized connectivity, in their brains.10 His team is now doing the prospective study he’s long hoped for—scanning the brains of 150 infants born with TSC and following them from birth to age 3 to try to determine why some develop autism and others don’t. He also plans to test therapies to see if it’s possible to prevent the development of autism in this highly susceptible population. In the first year of life, for example, TSC patients often develop epilepsy—another disorder marked by abnormalities in brain activity—so Sahin and colleagues will begin to treat the newborns with an epilepsy medication, and monitor how that affects the onset of autism.
“So far, studies done in humans have focused on relatively old individuals affected with autism, and they have not been that successful,” says Sahin. “Here, we have the capability of doing an intervention in children who don’t have autism yet, [to] see if we can prevent it.”
Prevention is a lofty goal when there are yet few treatments for autism. But as more details about the diverse disorder emerge, the potential for personalized treatments is gaining traction. Bernier and Eichler, for example, are planning a clinical trial of autism patients with a mutation in SCN2A, which encodes a sodium channel. They hope to test the effectiveness of a US Food and Drug Administration–approved medication that has successfully treated mice with sodium channel disruptions. Meanwhile, at Boston Children’s Hospital, Sahin is running a clinical trial studying biomarkers in children with autism and a PTEN mutation that disables a tumor suppressor in the body and has been linked to macrocephaly and language and social difficulties.
Bernier admits that a drug for one genetic subtype will likely be applicable to less than half of 1 percent of individuals with autism. But it’s something, he says. “If we can have a meaningful impact in a small group, that’s fine. Let’s just get started somewhere.”
And, perhaps, once a few treatments are discovered, autism research will once again follow in the footsteps of cancer research, where a drug approved for one cancer type subsequently proved beneficial in others, says Sahin. “We don’t have one form of autism we can treat yet, but hopefully one day soon we will have one or two forms. Then, we’ll see if others can benefit from those treatments.”
Megan Scudellari is a freelance science reporter in Boston, Massachusetts.