RNA ribozyme polymerases, dephosphorylases, restriction endoribo

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing compound containing saccharide radical

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4351723, 435193, 435194, 536 27, 935 3, 935 14, 502167, C12D 1934, C12N 1500, C12N 910, C12N 912, C07H 1512, B01J 3100

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049870718

ABSTRACT:
RNA enzymes or ribozymes can act as endoribonucleases, catalyzing the cleavage of RNA molecules with a sequence specificity of cleavage greater than that of known ribonucleases and approaching that of the DNA restriction endonucleases, thus serving as RNA sequence specific endoribonucleases. An example is a shortened form of the self-splicing ribosomal RNA intervening sequence of Tetrahymena (L-19 IVS RNA). Site-specific mutagenesis of the enzyme active site of the L-19 IVS RNA alters the substrate sequence specificity in a predictable manner, allowing a set of sequence-specific endoribonucleases to be synthesized. Varying conditions allow the ribozyme to act as a polymerase (nucleotidyltransferase), a dephosphorylase (acid phosphatase or phosphotransferase) or a sequence-specific endoribonuclease.

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The invention was made in part with government funds under Grant GM 28039 from the National Institutes of Health. Therefore, the U.S. Government has certain rights in the invention.

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