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Novel Gene Mutation Causes Huntington's-Like Symptoms, Providing Window Into How Brain Cells Die

Date:
October 21, 2002
Source:
Johns Hopkins Medical Institutions
Summary:
Researchers at Johns Hopkins have discovered a gene mutation that causes a condition apparently identical to Huntington's Disease, helping to explain why some people with the disorder do not have the mutation found in most cases. The finding may help reveal why some diseases, like Huntington's, Alzheimer's and Parkinson's, destroy some brain cells while sparing others.

"This is a rare version of an already rare disorder, but the mutation that causes it may not only help us better understand Huntington's Disease, but could boost our understanding of many other neurodegenerative disorders . . ." –Russell L. Margolis, M.D. Researchers at Johns Hopkins have discovered a gene mutation that causes a condition apparently identical to Huntington's Disease, helping to explain why some people with the disorder do not have the mutation found in most cases. The finding may help reveal why some diseases, like Huntington's, Alzheimer's and Parkinson's, destroy some brain cells while sparing others.

"For all practical purposes this is Huntington's Disease, yet it's caused by a different mutation on a completely different chromosome," said Russell L. Margolis, M.D., associate professor of Psychiatry at Hopkins and director of the Laboratory of Genetic Neurobiology.

The new mutation is in a gene called junctophilin-3 on chromosome 16, and the disorder it causes is called Huntington's Disease-like 2 (HDL2). The mutation that causes most Huntington's Disease cases is called huntingtin, and is found on chromosome 4, according to Margolis.

The scientists don't know how the new mutation affects the gene's function, but they do know that it leads to a pattern of brain cell death identical to Huntington's Disease: the same types of nerve cells are destroyed, the same regions of the brain, called the basal ganglia and the caudate nucleus, are targeted, and one side of the brain is affected more than the other. People with HDL2 also have the same types of changes in emotions, thinking, and decline in motor skills as those with Huntington's Disease. Like Huntington's, HDL2 occurs in mid-adult life and leads to death in about 10 to 20 years.

The type of mutation in the two genes is also similar. Both are repeat expansions, where a small segment of DNA, in this case three consecutive base-pairs, is repeated numerous times within the normal DNA chain. In HDL2, the more expanded repeats, or triplets, the mutation has, the earlier the age of onset of the disease.

So far, HDL2 has been diagnosed in 14 different families, most of African descent with a particularly high number of cases deriving from South Africa. Almost all of those with the disease have psychiatric symptoms, such as depression and personality changes, as a result of brain cell death.

"Knowing why some brain cells die and not others is crucial to figuring out how to intervene and stop or reverse the course of these diseases," said Margolis. "This is a rare version of an already rare disorder, but the mutation that causes it may not only help us better understand Huntington's Disease, but could boost our understanding of many other neurodegenerative disorders because we can now compare two different pathways leading to similar patterns of brain disease."

Margolis and his team will describe their findings in two presentations at the American Society for Human Genetics 2002 annual meeting in Baltimore, Md.

References:

Huntington's disease-like 2 (HDL2): Frequency, genotype-phenotype relationships, and neuropathological characterization. Thursday, October 17, 4:30-6:30 PM. Authors: R.L. Margolis, J. Troncoso, S.E. Holmes, E. O'Hearn, A. Rosenblatt, C. Callahan, J. Hwang, D. Rodnicki, C.A. Ross, A. Krauss, W. Seltzer.

Huntington's disease-like 2 (HDL2): Preliminary exploration of pathogenesis. Saturday, October 19, 10:45 AM - 12:45 PM. Authors: D. Rudnicki, E. O'Hearn, S.E. Holmes, A. Sawa, Z. Kaminsky, J. Kleiderlein, J. Troncoso, C.A. Ross, H. Takeshima, T.H. Moran, R.L. Margolis.


Story Source:

The above story is based on materials provided by Johns Hopkins Medical Institutions. Note: Materials may be edited for content and length.


Cite This Page:

Johns Hopkins Medical Institutions. "Novel Gene Mutation Causes Huntington's-Like Symptoms, Providing Window Into How Brain Cells Die." ScienceDaily. ScienceDaily, 21 October 2002. <www.sciencedaily.com/releases/2002/10/021021052011.htm>.
Johns Hopkins Medical Institutions. (2002, October 21). Novel Gene Mutation Causes Huntington's-Like Symptoms, Providing Window Into How Brain Cells Die. ScienceDaily. Retrieved July 28, 2014 from www.sciencedaily.com/releases/2002/10/021021052011.htm
Johns Hopkins Medical Institutions. "Novel Gene Mutation Causes Huntington's-Like Symptoms, Providing Window Into How Brain Cells Die." ScienceDaily. www.sciencedaily.com/releases/2002/10/021021052011.htm (accessed July 28, 2014).

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