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The gene identified by Rothman and UCSB postdoctoral researchers Tim Bloss and Eric Witze is called ICD-1 (inhibitor of cell death gene 1). It prevents normal cells from committing suicide.
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Read More »It is possible that such alternative routes are also used when cells inappropriately die in degenerative diseases. The researchers discovered that the protein coded by the ICD-1 gene normally hangs out in a compartment within the cell called the mitochondrion. "That was a gratifying discovery: the ICD-1 protein works in the organelle that is pivotal for the programmed suicide of cells," said Bloss. "Within the mitochondria, ICD-1 may keep the instruments of death that are loaded up in that organelle safely stowed away." The ICD-1 gene was discovered by studying a tiny roundworm called C. elegans. This worm was in the international spotlight last fall when the Nobel Prize in physiology or medicine was awarded to three scientists who pioneered its use for understanding normal development and programmed cell death in particular. The ICD-1 gene found in this animal is very closely related to a gene in humans, raising the possibility that its function may be altered in human degenerative diseases or cancer. "Hyperactivation of the human ICD-1 gene might well lead to tumor formation," notes Bloss, who was supported in part by a post-doctoral research fellowship from the Cancer Center of Santa Barbara. The findings have also allowed Rothman's team to discover other genes that act similarly to keep a check on the suicide of normal cells. Discovery of such genes could lead pharmaceutical companies to develop drugs for the treatment of cancer and degenerative diseases. The personal side of neurodegenerative diseases does not escape Rothman, who lost a family member to ALS a few years ago. "Our human state, including our ability to move, to feel emotion, and to be self-aware, all require an exquisitely honed nervous system," he said. "Progressive loss of our nerve cells chips away at who we are as humans."
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