Aminoacyl esterase activity of the Tetrahymena ribozyme

Science. 1992 Jun 5;256(5062):1420-4. doi: 10.1126/science.1604316.

Abstract

Several classes of ribozymes (catalytic RNA's) catalyze reactions at phosphorus centers, but apparently no reaction at a carbon center has been demonstrated. The active site of the Tetrahymena ribozyme was engineered to bind an oligonucleotide derived from the 3' end of N-formyl-methionyl-tRNA(fMet). This ribozyme catalyzes the hydrolysis of the aminoacyl ester bond to a modest extent, 5 to 15 times greater than the uncatalyzed rate. Catalysis involves binding of the oligonucleotide to the internal guide sequence of the ribozyme and requires Mg2+ and sequence elements of the catalytic core. The ability of RNA to catalyze reactions with aminoacyl esters expands the catalytic versatility of RNA and suggests that the first aminoacyl tRNA synthetase could have been an RNA molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Binding Sites
  • Carboxylic Ester Hydrolases / metabolism*
  • Kinetics
  • Models, Structural
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • Oligoribonucleotides
  • RNA, Catalytic / genetics
  • RNA, Catalytic / metabolism*
  • RNA, Transfer, Amino Acyl / metabolism
  • RNA, Transfer, Met*
  • Substrate Specificity
  • Tetrahymena / enzymology*

Substances

  • Oligoribonucleotides
  • RNA, Catalytic
  • RNA, Transfer, Amino Acyl
  • RNA, Transfer, Met
  • tRNA, formylmethionine-
  • Carboxylic Ester Hydrolases