Publication Type |
Journal Article |
School or College |
College of Science |
Department |
Human Genetics |
Creator |
Gesteland, Raymond F.; Atkins, John F.; Wills, Norma M. |
Other Author |
Fayet, G.; Peden J. |
Title |
Upstream stimulators for recoding |
Date |
1995 |
Description |
Recent progress in elucidation of 5' stimulatory elements for translational recoding is reviewed. A 5' Shine-Dalgarno sequence increases both +l and ? I frameshift efficiency in several genes; examples cited include the E. coli prfB gene encoding release factor 2 and the thuiX gene encoding the y and t subunits of DNA polymerase III holoenzyme. The spacing between the Shine-Dalgarno sequence and the shift site is critical in both the +l and ? 1 frameshift cassettes; however, the optimal spacing is quite different in the two cases. A frameshift in a mammalian chromosomal gene, ornithine decarboxylase antizyme, has recently been reported; 5' sequences have been shown to be vital for this frameshift event. Escherichia coli bacteriophage T4 gene 60 encodes a subunit of its type II DNA topoisomerase. The mature gene 60 mRNA contains an internal 50 nucleotide region that appears to be bypassed during translation. A 16 amino acid domain of the nascent peptide is necessary for this bypass to occur. |
Type |
Text |
Publisher |
National Research Council Canada Research Press |
First Page |
1123 |
Last Page |
1129 |
Subject |
Recoding; Frameshifting; Peptide factor; Stimulatory elements |
Subject MESH |
Frameshift Mutation; Genetics |
Language |
eng |
Bibliographic Citation |
Larsen, B., Peden, J., Matsufuji, S., Matsufuji, T., Brady, K., Maldonado, R., Wills, N.M., Fayet, O., Atkins, J.F., and Gesteland, R.F. 1995. Upstream stimulators for recoding. Biochem. Cell Biol. 73:1123-1129 |
Rights Management |
© National Research Council Canada Research Press |
Format Medium |
application/pdf |
Identifier |
ir-main,3723 |
ARK |
ark:/87278/s6t44bhq |
Setname |
ir_uspace |
ID |
704971 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6t44bhq |