Lead-catalyzed cleavage of yeast tRNAPhe mutants. 1990

L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215.

Yeast tRNA(Phe) lacking modified nucleotides undergoes lead-catalyzed cleavage between nucleotides U17 and G18 at a rate very similar to that of its fully modified counterpart. The rates of cleavage for 28 tRNA(Phe) mutants were determined to define the structural requirements of this reaction. The cleavage rate was found to be very dependent on the identity and correct positioning of the two lead-coordinating pyrimidines defined by X-ray crystallography. Nucleotide changes that disrupted the tertiary interactions of tRNAPhe reduced the rate of cleavage even when they were distant from the lead binding pocket. However, nucleotide changes designed to maintain tertiary interactions showed normal rates of cleavage, thereby making the reaction of a useful probe for tRNA(Phe) structure. Certain mutants resulted in the enhancement of cleavage at a "cryptic" site at C48. The sequences of Escherichia coli tRNA(Phe) and yeast tRNA(Arg) were altered such that they acquired the ability to cleave at U17, confirming our understanding of the structural requirements for cleavage. This mutagenic analysis of the lead cleavage domain provides a useful guide for similar analysis of autocatalytic self-cleavage reactions.

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D007854 Lead A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D009690 Nucleic Acid Conformation The spatial arrangement of the atoms of a nucleic acid or polynucleotide that results in its characteristic 3-dimensional shape. DNA Conformation,RNA Conformation,Conformation, DNA,Conformation, Nucleic Acid,Conformation, RNA,Conformations, DNA,Conformations, Nucleic Acid,Conformations, RNA,DNA Conformations,Nucleic Acid Conformations,RNA Conformations
D009691 Nucleic Acid Denaturation Disruption of the secondary structure of nucleic acids by heat, extreme pH or chemical treatment. Double strand DNA is "melted" by dissociation of the non-covalent hydrogen bonds and hydrophobic interactions. Denatured DNA appears to be a single-stranded flexible structure. The effects of denaturation on RNA are similar though less pronounced and largely reversible. DNA Denaturation,DNA Melting,RNA Denaturation,Acid Denaturation, Nucleic,Denaturation, DNA,Denaturation, Nucleic Acid,Denaturation, RNA,Nucleic Acid Denaturations
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA
D001665 Binding Sites The parts of a macromolecule that directly participate in its specific combination with another molecule. Combining Site,Binding Site,Combining Sites,Site, Binding,Site, Combining,Sites, Binding,Sites, Combining
D012345 RNA, Transfer, Amino Acid-Specific A group of transfer RNAs which are specific for carrying each one of the 20 amino acids to the ribosome in preparation for protein synthesis. Amino Acid-Specific Transfer RNA,Amino Acid-Specific tRNA,Transfer RNA, Amino Acid-Specific,tRNA-Amino Acid,RNA, Transfer, Amino Acid Specific,tRNA (Amino Acid),Acid, tRNA-Amino,Acid-Specific tRNA, Amino,Amino Acid Specific Transfer RNA,Amino Acid Specific tRNA,Transfer RNA, Amino Acid Specific,tRNA Amino Acid,tRNA, Amino Acid-Specific
D012360 RNA, Transfer, Phe A transfer RNA which is specific for carrying phenylalanine to sites on the ribosomes in preparation for protein synthesis. Phenylalanine-Specific tRNA,Transfer RNA, Phe,tRNAPhe,tRNA(Phe),Phe Transfer RNA,Phenylalanine Specific tRNA,RNA, Phe Transfer,tRNA, Phenylalanine-Specific

Related Publications

L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
September 1993, Biochemistry and molecular biology international,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
September 2000, FEBS letters,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
August 1979, European journal of biochemistry,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
January 1984, Postepy biochemii,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
July 1973, European journal of biochemistry,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
November 1999, The Journal of biological chemistry,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
May 1982, Biochemical and biophysical research communications,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
September 1978, Journal of molecular biology,
L S Behlen, and J R Sampson, and A B DiRenzo, and O C Uhlenbeck
January 1976, Biochimie,
Copied contents to your clipboard!