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An aging protein?


The same protein that, when defective, causes a premature-aging disease may also play a role in normal aging.

Children with Hutchinson Gilford Progeria progeria

Disorder with characteristics of premature aging. Affected persons have thin skin, go bald or gray early, and develop diseases of aging decades earlier than normal individuals.
 Syndrome (HGPS HGPS Hutchinson-Gilford Progeria Syndrome
HGPS Hemingford Grey Preservation Society (UK) 
) have maladies of aging, such as baldness and arthritis.

Yet "it hasn't been clear at the molecular level that this ...has anything to do with aging," says Tom Misteli of the National Cancer Institute (NCI See Liberate. ) in Bethesda, Md.

Misteli and his NCI coworker co·work·er or co-work·er  
n.
One who works with another; a fellow worker.
 Paola Scaffidi examined skin cells taken from HGPS patients and elderly people and found the samples to have similar defects.

Studies have identified a mutant version of the protein lamin A Lamin A is one of the intermediate filament proteins that weave together to form a shell called the nuclear lamina which lines the inner surface of the nucleus of every eukaryotic cell.  as the cause for HGPS. To see whether the defects in elderly patients' cells could be attributable to abnormal lamin A, the scientists applied a genetic technique that mends the defective protein. When the elderly patients' cells later divided, their offspring cells looked and behaved like cells taken from younger people, the researchers report in an upcoming Science.

Misteli and Scaffidi speculate that with age, cells might less successfully counter damage from this protein. Misteli says that it's too early to speculate about a treatment for human aging. "This is far from a miracle cure for anything,' he says.
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Article Details
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Title Annotation:BIOMEDICINE
Author:Brownlee, Christen
Publication:Science News
Article Type:Brief article
Date:May 13, 2006
Words:198
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