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Two new genes linked to intellectual disability discovered

Date:
March 31, 2014
Source:
Centre for Addiction and Mental Health
Summary:
Two new genes linked to intellectual disability have been discovered, according to two research studies. About one per cent of children worldwide are affected by non-syndromic (i.e., the absence of any other clinical features) intellectual disability, a condition characterized by an impaired capacity to learn and process new or complex information, leading to decreased cognitive functioning and social adjustment. Although trauma, infection and external damage to the unborn fetus can lead to an intellectual disability, genetic defects are a principal cause.

Researchers at the Centre for Addiction and Mental Health have discovered two new genes linked to intellectual disability, according to two research studies published concurrently this month in the journals Human Genetics and Human Molecular Genetics.

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"Both studies give clues to the different pathways involved in normal neurodevelopment," says CAMH Senior Scientist Dr. John Vincent, who heads the MiND (Molecular Neuropsychiatry and Development) Laboratory in the Campbell Family Mental Health Research Institute at CAMH. "We are building up a body of knowledge that is informing us which kinds of genes are important to, and involved in, intellectual disabilities."

In the first study, Dr. Vincent and his team used microarray genotyping to map the genes of a large Pakistani family which had intermarriage. Five members of the youngest generation were affected with mild to moderate intellectual disability. Dr. Vincent identified a truncation in the FBXO31 gene, which plays a role in the way that proteins are processed during development of neurons, particularly in the cerebellar cortex.

In the second study, using the same techniques, Dr. Vincent and his team analyzed the genes of two families with intermarriage, one Austrian and one Pakistani, and identified a disruption in the METTL23 gene linked to mild recessive intellectual disability. The METTL23 gene is involved in methylation -- a process important to brain development and function.

About one per cent of children worldwide are affected by non-syndromic (i.e., the absence of any other clinical features) intellectual disability, a condition characterized by an impaired capacity to learn and process new or complex information, leading to decreased cognitive functioning and social adjustment. Although trauma, infection and external damage to the unborn fetus can lead to an intellectual disability, genetic defects are a principal cause.

These studies were part of an ongoing study of affected families in Pakistan, where the cultural tradition of large families and consanguineous (inter-) marriages among first cousins increases the likelihood of inherited intellectual disability in offspring.

"Although it is easier to find and track genes in consanguineous families, these genes are certainly not limited to them," Dr. Vincent points out. A recent study estimated that 13󈞄 per cent of intellectual disability cases among individuals of European descent are caused when an individual inherits two recessive genes, meaning that results of this study are very relevant to populations such as Canada.

This type of autosomal recessive gene mutation haas traditionally been more difficult to trace, resulting in a paucity of research in this area. Parents of affected children show no symptoms, and the child must inherit one defective copy of the gene from each parent, so that only one in four offspring are likely to be affected. Smaller families, therefore, show a decreased frequency and are less amenable to this kind of study.

Dr. Vincent is currently engaged in a study that will screen Canadian populations of autism and intellectual disability for autosomal recessive gene mutations. Results will be available later this year.

A total of 42 genes linked to non-syndromic recessive forms of intellectual disability have now been identified; estimates suggest that up to 2,500 genes might be linked with intellectual disability, the majority being recessive.


Story Source:

The above story is based on materials provided by Centre for Addiction and Mental Health. Note: Materials may be edited for content and length.


Journal References:

  1. Asif Mir, Kumudesh Sritharan, Kirti Mittal, Nasim Vasli, Carolina Araujo, Talal Jamil, Muhammad Arshad Rafiq, Zubair Anwar, Anna Mikhailov, Sobiah Rauf, Huda Mahmood, Abdul Shakoor, Sabir Ali, Joyce So, Farooq Naeem, Muhammad Ayub, John B. Vincent. Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family. Human Genetics, 2014; DOI: 10.1007/s00439-014-1438-0
  2. M. Bernkopf, G. Webersinke, C. Tongsook, C. N. Koyani, M. Arshad, M. Ayaz, D. Muller, C. Enzinger, M. Aslam, F. Naeem, K. Schmidt, K. Gruber, M. R. Speicher, E. Malle, P. Macheroux, M. Ayub, J. B. Vincent, C. Windpassinger, H.-C. Duba. Disruption of the Methyltransferase-Like 23 Gene METTL23 Causes Mild Autosomal Recessive Intellectual Disability. Human Molecular Genetics, 2014; DOI: 10.1093/hmg/ddu115

Cite This Page:

Centre for Addiction and Mental Health. "Two new genes linked to intellectual disability discovered." ScienceDaily. ScienceDaily, 31 March 2014. <www.sciencedaily.com/releases/2014/03/140331114332.htm>.
Centre for Addiction and Mental Health. (2014, March 31). Two new genes linked to intellectual disability discovered. ScienceDaily. Retrieved October 25, 2014 from www.sciencedaily.com/releases/2014/03/140331114332.htm
Centre for Addiction and Mental Health. "Two new genes linked to intellectual disability discovered." ScienceDaily. www.sciencedaily.com/releases/2014/03/140331114332.htm (accessed October 25, 2014).

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