Title |
Readthrough of dystrophin stop codon mutations induced by aminoglycosides
|
---|---|
Published in |
Annals of Neurology, January 2004
|
DOI | 10.1002/ana.20052 |
Pubmed ID | |
Authors |
Michael T. Howard, Christine B. Anderson, Uwe Fass, Shikha Khatri, Raymond F. Gesteland, John F. Atkins, Kevin M. Flanigan |
Abstract |
We report the translational readthrough levels induced by the aminoglycosides gentamicin, amikacin, tobramycin, and paromomycin for eight premature stop codon mutations identified in Duchenne's and Becker's muscular dystrophy patients. In a transient transfection reporter assay, aminoglycoside treatment results show that one stop codon mutation is suppressed significantly better (up to 10% stop codon readthrough) than the others; five show lower but statistically significant suppression (< 2% stop codon readthrough); and two appear refractory to aminoglycoside treatment. Readthrough levels do not substantially vary between different sources of gentamicin, and, for this set of mutations, the efficiency of termination at the premature stop codon mutation does not appear to correlate with disease severity. |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 2 | 2% |
Israel | 1 | 1% |
Netherlands | 1 | 1% |
Unknown | 77 | 95% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 20 | 25% |
Researcher | 14 | 17% |
Student > Master | 10 | 12% |
Student > Bachelor | 8 | 10% |
Professor | 7 | 9% |
Other | 13 | 16% |
Unknown | 9 | 11% |
Readers by discipline | Count | As % |
---|---|---|
Agricultural and Biological Sciences | 34 | 42% |
Biochemistry, Genetics and Molecular Biology | 14 | 17% |
Chemistry | 9 | 11% |
Medicine and Dentistry | 6 | 7% |
Social Sciences | 2 | 2% |
Other | 6 | 7% |
Unknown | 10 | 12% |