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Jackson Laboratory Researchers Identify Neuromuscular Degeneration Gene

Date:
December 23, 1998
Source:
The Jackson Laboratory
Summary:
Scientists at The Jackson Laboratory have cloned the gene for the mouse mutation known as neuromuscular degeneration, or nmd, an advance that promises to boost research into such devastating neurological diseases in humans as amyotrophic lateral sclerosis and spinal muscular atrophy.

Bar Harbor -- Scientists at The Jackson Laboratory have cloned the gene for the mouse mutation known as neuromuscular degeneration, or nmd, an advance that promises to boost research into such devastating neurological diseases in humans as amyotrophic lateral sclerosis and spinal muscular atrophy.

The results are published in a research paper, "Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele," in the December 1998 issue of the scientific journal Neuron. The Jackson Laboratory team was led by Dr. Gregory A. Cox, Dr. Wayne N. Frankel and Connie L. Mahaffey.

"There are no effective treatments for these diseases, and the underlying causes of neurodegeneration remain obscure," said Dr. Cox, a Research Scientist in Dr. Frankel's group. "Mouse models of human disease like nmd provide unique tools for both gene discovery and analysis of underlying disease mechanisms. Our findings provide a new tool for understanding the complex process of motor neuron death."

In another significant finding, the researchers report that severity of the nmd's disease traits is suppressed by a modifier gene mapped to a locus (Mnm) on mouse Chromosome 13. The existence of such modifier genes has long been suspected in human ALS and SMA because of observed heterogeneity in age of onset and/or severity of symptoms.

The nmd mouse was originally discovered at The Jackson Laboratory and reported in Mammalian Genome (March 1995) by researchers Susan A. Cook and Drs. Kenneth R. Johnson, Roderick T. Bronson, and Muriel T. Davisson. The mutation causes severe muscle atrophy due to progressive degeneration of spinal motor neurons, which control the movement of voluntary muscles. The mice exhibit progressive paralysis that initially begins with the hindlimbs. Variable forelimb paralysis occurs in later stages of the disease, with life expectancy rarely exceeding four weeks.

Similar motor neuron degeneration is implicated in amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA). ALS, or "Lou GehrigΉs Disease," is a fatal neurological disorder that attacks motor cells in the spinal cord and brain. The disease affects up to 30,000 people in the United States. About 5-10% of ALS cases are classified as familial and are suspected of having a genetic defect in a specific chromosome.

Spinal muscular atrophy, also characterized by degeneration of motor cells in the spinal cord and brain, is the second most common neuromuscular disorder of childhood, after Duchenne Muscular Dystrophy. SMA has three major childhood forms classified by age of onset. Most forms are genetic, and at least one gene involved in SMA has been identified on human chromosome 5q.

The Neuron paper reports that the defective gene (designated Smbp2) in the neuromuscular disease mice encodes a DNA-binding protein (SMBP2, or immunoglobulin S-mu binding protein-2) on chromosome 19. The new findings are the first indication of an essential role for the protein in motor neuron function and survival, although different laboratories have previously identified other roles for SMBP2.

Proteins in the family to which SMBP2 belongs (known as the DNA helicase/ATPase family), are known to be involved in many cellular activities, including DNA replication, repair, and recombination. The gene encoding SMBP2 is widely expressed, with high levels in brain, heart, kidney, spleen, and testes, and lower levels in pancreas, liver, lung, and salivary gland.

"The selective degeneration of motor neurons in this model and the dramatic effect that the single Mnm modifier gene has on the onset and progression of disease in the nmd mouse suggest that targets for intervention in motor neuron disease exist that can be manipulated to alter disease progression," Dr. Cox said.

The research at The Jackson Laboratory was supported in part by grants to Dr. Cox from the National Institutes of Health and the Amyotrophic Lateral Sclerosis Association, and to Dr. Frankel from the National Institutes of Health and the Klingenstein Fellowship in the Neurosciences.

*******************

The Jackson Laboratory, founded in 1929, is a world leader in mammalian genetics research. With more than 850 employees, the nonprofit, independent facility has a three-fold mission: to conduct basic genetic and biomedical research, train present and future scientists, and provide genetic resources to researchers worldwide.


Story Source:

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


Cite This Page:

The Jackson Laboratory. "Jackson Laboratory Researchers Identify Neuromuscular Degeneration Gene." ScienceDaily. ScienceDaily, 23 December 1998. <www.sciencedaily.com/releases/1998/12/981223081401.htm>.
The Jackson Laboratory. (1998, December 23). Jackson Laboratory Researchers Identify Neuromuscular Degeneration Gene. ScienceDaily. Retrieved September 17, 2014 from www.sciencedaily.com/releases/1998/12/981223081401.htm
The Jackson Laboratory. "Jackson Laboratory Researchers Identify Neuromuscular Degeneration Gene." ScienceDaily. www.sciencedaily.com/releases/1998/12/981223081401.htm (accessed September 17, 2014).

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