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Common Variation in a Gene Could Cause Structural Alterations in the Brain

by Savitha C Muppala on  August 20, 2009 at 11:36 PM Research News   - G J E 4
 Common Variation in a Gene Could Cause Structural Alterations in the Brain
Variations in a gene known to cause Retts Syndrome, autism, and mental retardation is also said to be behind the differences in brain structure in both healthy individuals and patients with neurological and psychiatric disorders, says a report.
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"We studied not only the gene itself - a gene called MECP2, which is known to have a big effect on brain development - but also the regions surrounding the gene, sometimes known as junk DNA," said principle investigator Dr. Anders M. Dale, professor of Neurosciences and Radiology at the University of California, San Diego School of Medicine.

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"Looking at this 'bigger window' of genetic data, we discovered that common variations in the MECP2 region result in changes to brain structure, even in healthy individuals," Dale added.

The international team of researchers behind the study say that the link between genetics and brain structure is a hotly debated area of research.

They highlight the fact that past studies investigating the link between gene variations and human brain structure have not used the types of refined brain measurements provided by the structural MRI scans and software developed at UC San Diego, or the and full genetic coverage included in the PNAS study.

Led by Ole A. Andreassen at Ullelval University Hospital and Institute of Psychiatry in Oslo, Norway, the research team provided data on one cohort - a sample from the Thematic Organized Psychosis (TOP) research group.

The data was compared to a sample from the Alzheimer's Disease Neuroimaging Initiative (ADNI), the largest Alzheimer's disease study ever funded by the National Institutes of Health, in studies conducted at UC San Diego.

The researchers looked at 289 healthy and psychotic subjects from the TOP study, and 655 healthy and demented patients, largely with Alzheimer's disease, from the ADNI study.

"The most statistically significant association between the two groups involved a minor allele of a single polymorphism, an inherited genetic variation that is found in more than one percent of the population. This variation resulted in structural brain changes, such as reduced surface area in the brain's cortex, the area that plays a key role in memory, attention, perceptual awareness, thought and language," said co-author Dr. Nicholas J. Schork, of the Scripps Translational Science Institute.

Although expressed in all cells, the researchers say that the MECP2 gene is developmentally regulated and exists in two different genetic transcripts within the brain's neuronal cells.

According to them, changes in brain structure caused by this gene are specific to males, since the variation is found on the X chromosome, but the functional, cognitive consequences aren't yet known.

Dale says that the fact that broader, common variations in the area surrounding the MECP2 gene also resulted in changes to the brain structure suggests that this gene may be a promising candidate gene for further study.

"Since each individual genetic mutation causes only small changes, the so-called 'junk DNA' may be where the action is," he said.

He says that these regions may not change the gene or the protein it encodes, but change the regulation of the gene.

A research article describing the study has been published in the early online edition of the Proceedings of the National Academy of Sciences.

Source: ANI
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