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PMID: 10508413 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Minimum requirements for substrates of mammalian tRNA 3' processing endoribonuclease.

Biochemistry ·Vol. 38 ·No. 37 ·1999-09-14 ·Pages 12089-96

Nashimoto M, Tamura M, Kaspar RL

Abstract

Mammalian tRNA 3' processing endoribonuclease (3' tRNase) removes a 3' trailer after the discriminator nucleotide from precursor tRNA (pre-tRNA). To elucidate the minimum requirements for 3' tRNase substrates, we tested small pre-tRNA(Arg) substrates lacking the D and anticodon stem-loop domain for cleavage by purified pig 3' tRNase. A small pre-tRNA (R-ATW) composed of an acceptor stem, an extra loop, a T stem-loop domain, a discriminator nucleotide, and a 3' trailer was cleaved more efficiently than the full-length wild type. The catalytic efficiencies of three R-ATW derivatives, which were constructed to destroy the original T stem base pairs, were also higher than that of the full-length wild type. Pig 3' tRNase efficiently processed a "minihelix" (R-ATM5) that consists of a T stem-loop domain, an acceptor stem, a discriminator nucleotide, and a 3' trailer, while the enzyme never cleaved a "microhelix" that is composed of a T loop, an acceptor stem, a discriminator nucleotide, and a 3' trailer. Five R-ATM5 derivatives that have one to seven base substitutions in the T loop were all cleaved slightly more efficiently than the full-length wild type and slightly less efficiently than R-ATM5. A helix ("minihelixDelta1") one base pair smaller than minihelices was a good substrate, while small helices containing a continuous 10-base pair stem were poor substrates. The cleavage of these three small substrates occurred after the discriminator and one to three nucleotides downstream of the discriminator. From these results, we conclude that minimum substrates for efficient cleavage by mammalian 3' tRNase are minihelices or minihelicesDelta1, in which there seem to be no essential bases.

MeSH Terms
Animals Anticodon/genetics Base Pairing Conserved Sequence Endoribonucleases/metabolism Evolution, Molecular Hydrolysis Nucleic Acid Conformation RNA Precursors/genetics,metabolism RNA Processing, Post-Transcriptional/genetics RNA, Transfer, Arg/genetics,metabolism Substrate Specificity/genetics Swine
Chemicals
Anticodon RNA Precursors RNA, Transfer, Arg pre-tRNA(Arg) Endoribonucleases 3'-pre-tRNase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nashimoto M
Department of Chemistry and Biochemistry, Brigham Young University, Provo, Utah 84602, USA. mnashimoto@chemgate.byu.edu
Tamura M
Kaspar R L
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1999-09-14
Pages
12089-96
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM57644 · United States
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