GEN Exclusives

More »

GEN News Highlights

More »
Dec 7, 2012

Novel Genetic Pathway May Underlie Neurodevelopmental Disorders

  • Scientists at the Douglas Mental Health University Institute report the discovery of a new genetic process that they say might one day provide a novel target for the treatment of neurodevelopmental disorders, such as intellectual disability and autism.

    The research study, which appears in the December issue of the American Journal of Human Genetics, was led by Carl Ernst, Ph.D., a Douglas Institute researcher and an assistant professor in McGill University’s department of psychiatry. He and his colleagues found that genetic mutations that negatively affect brain development can occur in a gene family of previously unknown function in the human genome.

    According to the World Health Organization, neurodevelopmental disorders affect one in six children in industrialized countries. Impairing the growth and development of the brain or central nervous system, neurodevelopmental disorders encompass a broad range of conditions, including developmental delay, autism spectrum disorders, and cerebral palsy. People with neurodevelopmental disorders can experience difficulties with language, speech, learning, behavior, motor skills, and memory.

    Mutations in genes are thought to underlie many neurodevelopmental disorders, but all genes important for brain development found to date are in a single pathway. Prior to the current study, all genetic mutations important for neurodevelopmental disorders occurred in genes that make protein.

    The work of the Ernst team identified an important shortcut in the process of making functional molecules for brain development. By sequencing the genomes of 200 people with neurodevelopmental disorders and chromosomal abnormalities, and comparing the results to more than 15,000 control samples, the researchers made a surprising discovery: some individuals had mutations in a gene that did not make protein.

    "Our discovery tells us that mutations in genes that code only for RNA and do not make protein can have a functional impact and lead to neurodevelopmental abnormalities," says Dr. Ernst. "In previous studies of brain development, RNA was just considered a middle player, one that only served as a template for the production of proteins."

    By opening up a new area of study involving RNA, the Ernst group aims to advance understanding of the underlying causes of neurodevelopmental disorders. "We hope to shine a new light on how the brain develops," he says.


Add a comment

  • You must be signed in to perform this action.
    Click here to Login or Register for free.
    You will be taken back to your selected item after Login/Registration.

Related content

Jobs

GEN Jobs powered by HireLifeScience.com connects you directly to employers in pharma, biotech, and the life sciences. View 40 to 50 fresh job postings daily or search for employment opportunities including those in R&D, clinical research, QA/QC, biomanufacturing, and regulatory affairs.
 Searching...
More »

GEN Poll

More » Poll Results »

Connectomics Advocacy

How might connectomics maintain lasting support?