CONFERENCES The international research workshop Kant’s Project of Perpetual Peace in the Context of Modern Politics (Kaliningrad, April 20—22, 2012) On April 20—22, 2012, international research workshop Kant’s Project of Per- petual Peace In the context of Modern Politics was held at the Immanuel Kant Baltic Federal University. It was organised by the Ka
Microbio.uab.eduThe Scientist - Antibiotic Corrects Genetic Glitch The Scientist 15:16, Apr. 16, 2001
Antibiotic Corrects Genetic Glitch
By Ricki Lewis
Antibiotics that enable ribosomes to "read through" premature stop codons (nonsense mutations), which truncate proteins, may kick-start a new approach to gene therapy. A team of researchers from the University of Alabama at Birmingham and from the Women's and Children's Hospital in South Australia applied a long-ago observation about the antibiotic gentamicin on ribosomes to correct the enzyme deficiency that causes Hurler syndrome, in cultured fibroblasts from patients.1 The antibiotic apparently enables ribosomes to zip past nonsense mutations,
in which a single base substitution converts an amino-acid encoding codon into a stop codon, shortening the
protein product. "It's been known since the early 1960s that aminoglycoside antibiotics bind the 16S bacterial
ribosomal RNA subunit, affecting translational fidelity, causing read-through of stop codons in bacteria. In
mammalian ribosomes, the region is similar but it has a lower binding affinity, and that's why these antibiotics kill
bacteria before they kill people. We show that the concentrations of antibiotic used clinically to kill bacteria are
tweaking mammalian ribosomes," explains David M.
Bedwell associate professor of microbiology at the
The symptoms of Hurler syndrome--mental retardation, dwarfism, hearing loss, enlarged liver and spleen, and cardiac and respiratory problems--stem from deficiency of alpha-L-iduronidase, which normally breaks down glycosaminoglycans (a type of mucopolysaccharide) in the lysosomes of fibroblasts and white blood cells. Just a modest boost in enzyme production can lessen the severity of symptoms, but attempts at enzyme replacement therapy have failed. The researchers focused on Hurler syndrome because nearly two-thirds of the known mutations are nonsense. However, the investigators and others have also used the antibiotic to suppress nonsense mutations in cells from patients with cystic fibrosis,4 and in mice with muscular dystrophy.5 "This approach has tremendous potential. Aminoglycosides are just one type of antibiotic, and it works," says Bedwell. PTC Therapeutics of South Plainfield, NJ, is one step ahead--they are using high throughput assays to discover variations on the gentamicin theme that do not bring the side effects of kidney and ear toxicity.
Bedwell likens this new use for an old drug to the Viagra saga, where "a funny side effect led to a huge new market. You have to keep your eyes open and if you know the molecular mechanism, you can zero in on a treatment." References
1. K. Keeling et al., "Gentamicin-mediated suppression of Hurler syndrome stop mutations leads to a partial restoration of a-L-iduronidase
activity and a reduction of lysosomal glycosaminoglycan accumulation,"
2. J. Davies et al., "Misreading of RNA codewords induced by aminoglycoside antibiotics," 3. E.M. Lederberg et al., "Interaction of streptomycin and a suppressor for galactose fermentation in E. coli K-12," Proceedings of the 4. M. Wilschanski et al., "A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations," American Journal of Respiratory Critical Care Medicine 5. E.R. Barton-Davis et al., "Aminoglycoside antibiotics restore dystrophin function to skeletal muscles of mdx mice," Journal of Clinical The Scientist 15:16, Apr. 16, 2001
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