Autism genetics expert Ivan Iossifov breaks down recent research that sheds light on how unaffected parents can pass autism onto their child.
Parents with no history of autism in their families have a child who is diagnosed with the disorder. It鈥檚 a common and upsetting story.A quick Google search for 鈥渁utism causes鈥 is all it takes to learn that scientists believe the disorder has a strong genetic component. So if there鈥檚 no genetic history in the family, where does a child鈥檚 autism come from?
A key fact has come to light within the last couple of years: many autism-causing genetic mutations are 鈥渟pontaneous.鈥 They occur in the affected child, but in neither parent. Mutations in this category 鈥渁re not directly inherited from the parents,鈥 explains Assistant Professor Ivan Iossifov, one of several CSHL scientists who has pioneered the study of the role of spontaneous mutations in autism causation.
A child鈥檚 genome is a patchwork stitched together from the genetic 鈥渃loth鈥 contained in the mother鈥檚 egg and father鈥檚 sperm. In theory, that means that children are cut from exactly the same cloth as their parents. But in reality, there are virtually always small 鈥渇actory defects鈥 in that cloth鈥攎utations that spontaneously arise during the sperm or egg鈥檚 creation.
Spontaneous mutations cause as much as half of all autism in situations in which only one child in the family has autism. This and other analysis comes from a study Iossifov published in 2015. He and his team looked at about 2,500 families with a single affected child and investigated the causal link to spontaneous mutations.
Professor Michael Wigler explains the genetic factors at play in his 鈥渦nified theory of autism”
As Iossifov says, all of us have such mutations, and usually they have no effect at all. Humans normally have two copies of every gene, even though only one working copy typically necessary for proper functioning.
鈥淲e have two copies of most genes for a reason鈥攊t鈥檚 kind of a buffer,鈥 says Iossifov.
This buffer protects us from spontaneous mutations in many of our genes. Iossifov and CSHL collaborator Michael Wigler theorize, however, that autism 鈥渞isk genes鈥 are particularly vulnerable to mutations. One reason is that for such genes, a person must have two working copies to function normally. As a result, a spontaneous mutation in one of these autism risk genes tends to have devastating effects.
Other major potential explanations for sporadic autism are also actively being studied, Iossifov notes, including other genetic causes and the role of factors in a child鈥檚 environment.
Read this next: What do autism “risk genes” do?
Note: For the sake of simplicity, this article uses the term 鈥榓utism鈥 to refer to all autism spectrum disorders (ASDs). You can find out more about the distinction between autism and ASD here.