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Mol Cell Biol, March 1998, p. 1459-1466, Vol. 18, No. 3
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Initiator-Elongator Discrimination in Vertebrate
tRNAs for Protein Synthesis
Harold J.
Drabkin,
Melanie
Estrella, and
Uttam L.
Rajbhandary*
Department of Biology, Massachusetts
Institute of Technology, Cambridge, Massachusetts 02139
Received 24 October 1997/Returned for modification 5 December
1997/Accepted 12 December 1997
Initiator tRNAs are used exclusively for initiation of protein
synthesis and not for the elongation step. We show, in vivo and in
vitro, that the primary sequence feature that prevents the human
initiator tRNA from acting in the elongation step is the nature of base
pairs 50:64 and 51:63 in the T
C stem of the initiator tRNA. Various
considerations suggest that this is due to sequence-dependent
perturbation of the sugar phosphate backbone in the T
C stem of
initiator tRNA, which most likely blocks binding of the elongation
factor to the tRNA. Because the sequences of all vertebrate initiator
tRNAs are identical, our findings with the human initiator
tRNA are likely to be valid for all vertebrate systems. We have
developed reporter systems that can be used to monitor, in mammalian
cells, the activity in elongation of mutant human initiator tRNAs
carrying anticodon sequence mutations from CAU to CCU (the C35 mutant)
or to CUA (the U35A36 mutant). Combination of the anticodon sequence
mutation with mutations in base pairs 50:64 and 51:63 yielded tRNAs
that act as elongators in mammalian cells. Further mutation of the
A1:U72 base pair, which is conserved in virtually all eukaryotic
initiator tRNAs, to G1:C72 in the C35 mutant background yielded tRNAs
that were even more active in elongation. In addition, in a rabbit
reticulocyte in vitro protein-synthesizing system, a tRNA carrying the
T
C stem and the A1:U72-to-G1:C72 mutations was almost as active in
elongation as the elongator methionine tRNA. The
combination of mutant initiator tRNA with the CCU anticodon and the
reporter system developed here provides the first example of missense
suppression in mammalian cells.
*
Corresponding author. Mailing address: Department of
Biology, 68-671A, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139. Phone: (617) 253-4702. Fax:
(617) 252-1556. E-mail: bhandary{at}wccf.mit.edu.
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