NARSAD Investigator Defines New Genetic Variations in Autism

Printer-friendly versionPrinter-friendly version
DNA sequence
DNA sequence
Catalina Betancur, M.D., Ph.D., NARSAD 2010 Independent Investigator applies neuroscience, genetic and clinical training to identify role of rare genetic variations in Autism

NARSAD Independent Investigator Dr. Catalina Betancur has succeeded in finding powerful but uncommon "one-hit" genetic errors in a growing number of autism patients who have taken part in studies in which she is involved.

As a result, Betancur has enjoyed what for a research scientist is perhaps the rarest of satisfactions: with the help of clinical geneticists, she has shared precise knowledge of disease causation in specific cases with families of affected individuals. "We've had this opportunity several times, and it is really wonderful - this is information that can truly be life-changing for a family."

Betancur participates in two important autism projects in France, where she is an Investigator at INSERM, the French equivalent of America's National Institutes of Health. At her lab in Paris, she has access to patients enrolled in the Paris Autism Research International Study (PARIS) and participates in the multinational Autism Genome Project (AGP), a large-scale study involving thousands of autism patients, their relatives and healthy controls.

Her goal is to learn how very rare genetic variations perturb the biology of the developing brain to cause the wide range of symptoms - from severe and debilitating to comparatively mild - seen across autism spectrum disorders, or ASDs.

Betancur not only scrutinized DNA samples of people with ASDs; she also makes a point of examining carefully the clinical information about the individuals she studies. She begins from clinical signs and works her way back toward the genetic mutations that are the root cause. She's well-suited for this task, having been trained in clinical medicine and neuroscience and genetics. Betancur, whose father is a neurologist, remembers "always wanting to be a doctor, like him," but being interested also in "the question of how the brain works." After earning a M.D. in her native Colombia, she pursued a Ph.D. in neuroscience in France, and then began to study autism.

"We find many rare variations in patients with ASDs. But we don't know at the beginning if they're important - if they occur in a place in the genome where they might give rise to pathology." An extraordinary process of winnowing ensues, involving high-tech genome sequencing, clinical work-ups of patients, family interviews and neurobiology studies. "When we find a candidate genome variation, we do experiments to determine if this area contains a gene of importance in brain development."

Knowing genes and pathways involved in ASDs is the starting point for development of future therapies. It is also a basis for the genetic counseling that Betancur and colleagues have seen change lives. If a rare variant found to cause autism is de novo - if it occurred spontaneously in the fertilized egg at the time of conception - then by definition, the parents are not carriers, nor are any other relatives. If a variant is inherited, then it has precise implications for parents, siblings, even cousins. "This is information that helps everyone make reproductive decisions. And being able to help families is what makes me absolutely passionate about the work I'm pursuing with my new NARSAD grant," Betancur says.

Article comments

My brother adopted a little girl who is autistic. He has since learned that her older brother and younger sister are also autistic. The older brother is also cruel/violent. The parents reason for giving up their newborn little girl (my niece), was due to the brother. They were afraid he would harm the baby. The mother later had another little girl with a different husband, and she kept that baby (even though the son lived in the same house). It was an open adoption, so my niece has contact with the siblings. My niece told me her sister and brother have autism like her. My niece said she doesn't like her brother and is afraid of him. She states he is mean, no one can control him and she is glad he doesn't know where she lives. Since one child was born away from the family and has problems I think genetic counseling could help couples like them make informed choices.

Add new comment

comments

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.

Please note that researchers cannot give specific recommendations or advice about treatment; diagnosis and treatment are complex and highly individualized processes that require comprehensive face-to- face assessment. Please visit our "Ask an Expert" section to see a list of Q & A with NARSAD Grantees.
By submitting this form, you accept the Mollom privacy policy.