Nucleic Acids Research Advance Access published online on October 16, 2008
Nucleic Acids Research, doi:10.1093/nar/gkn703
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Synthesis and investigation of the 5-formylcytidine modified, anticodon stem and loop of the human mitochondrial tRNAMet
1Department of Chemistry, 2Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC 27695 and 3Dharmacon, 2650 Crescent Drive #100, Lafayette, CO 80026, USA
*To whom correspondence should be addressed. Tel: +1 919 515 6188; Fax: +1 919 515 2047; Email: Paul_Agris{at}ncsu.edu
Correspondence may also be addressed to Alexander Deiters. Tel: +1 919 513 2958; Fax: +1 919 515 5079; Email: Alex_Deiters{at}ncsu.edu
Received July 29, 2008. Revised September 28, 2008. Accepted September 29, 2008.
Human mitochondrial methionine transfer RNA (hmtRNA
) has a unique post-transcriptional modification, 5-formylcytidine, at the wobble position-34 (f5C34). The role of this modification in (hmtRNA
) for the decoding of AUA, as well as AUG, in both the peptidyl- and aminoacyl-sites of the ribosome in either chain initiation or chain elongation is still unknown. We report the first synthesis and analyses of the tRNA's anticodon stem and loop domain containing the 5-formylcytidine modification. The modification contributes to the tRNA's anticodon domain structure, thermodynamic properties and its ability to bind codons AUA and AUG in translational initiation and elongation.
The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.
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