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Critical role of one gene to our brain development

Date:
March 14, 2014
Source:
University of Adelaide
Summary:
A gene linked to intellectual disability is critical to the earliest stages of the development of human brains, new research has confirmed. An international research team explains in a new paper how mutations in USP9X are associated with intellectual disability. These mutations, which can be inherited from one generation to the next, have been shown to cause disruptions to normal brain cell functioning.

Research from the University of Adelaide has confirmed that a gene linked to intellectual disability is critical to the earliest stages of the development of human brains.

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Known as USP9X, the gene has been investigated by Adelaide researchers for more than a decade, but in recent years scientists have begun to understand its particular importance to brain development.

In a new paper published online in the American Journal of Human Genetics, an international research team led by the University of Adelaide's Robinson Research Institute explains how mutations in USP9X are associated with intellectual disability. These mutations, which can be inherited from one generation to the next, have been shown to cause disruptions to normal brain cell functioning.

Speaking during Brain Awareness Week, senior co-author Dr Lachlan Jolly from the University of Adelaide's Neurogenetics Research Program says the USP9X gene has shed new light on the mysteries of brain development and disability.

Dr Jolly says the base framework for the brain's complex network of cells begins to form at the embryo stage.

"Not surprisingly, disorders that cause changes to this network of cells, such as intellectual disabilities, epilepsy and autism, are hard to understand, and treat," Dr Jolly says.

"By looking at patients with severe learning and memory problems, we discovered a gene -- called USP9X -- that is involved in creating this base network of nerve cells. USP9X controls both the initial generation of the nerve cells from stem cells, and also their ability to connect with one another and form the proper networks," he says.

"This work is critical to understanding how the brain develops, and how it is altered in individuals with brain disorders.

"We hope that by learning more about genes such as USP9X, we will create new opportunities to understand brain disorders at a much deeper level than currently known, which could lead to future treatment opportunities."


Story Source:

The above story is based on materials provided by University of Adelaide. Note: Materials may be edited for content and length.


Journal Reference:

  1. ClaireC. Homan, Raman Kumar, LamSon Nguyen, Eric Haan, F.Lucy Raymond, Fatima Abidi, Martine Raynaud, Charles E. Schwartz, StephenA. Wood, Jozef Gecz, LachlanA. Jolly. Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth. The American Journal of Human Genetics, 2014; 94 (3): 470 DOI: 10.1016/j.ajhg.2014.02.004

Cite This Page:

University of Adelaide. "Critical role of one gene to our brain development." ScienceDaily. ScienceDaily, 14 March 2014. <www.sciencedaily.com/releases/2014/03/140314095056.htm>.
University of Adelaide. (2014, March 14). Critical role of one gene to our brain development. ScienceDaily. Retrieved November 22, 2014 from www.sciencedaily.com/releases/2014/03/140314095056.htm
University of Adelaide. "Critical role of one gene to our brain development." ScienceDaily. www.sciencedaily.com/releases/2014/03/140314095056.htm (accessed November 22, 2014).

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