|
Originally published In Press as doi:10.1074/jbc.M212890200 on March 13, 2003
J. Biol. Chem., Vol. 278, Issue 20, 17672-17679, May 16, 2003
Common Location of Determinants in Initiator Transfer RNAs for
Initiator-Elongator Discrimination in Bacteria and in Eukaryotes*
Alexei
Stortchevoi,
Umesh
Varshney , and
Uttam L.
RajBhandary§
From the Department of Biology, Massachusetts Institute of
Technology, Cambridge, Massachusetts 02139
Initiator tRNAs are used exclusively for
initiation of protein synthesis and not for elongation. We show that
both Escherichia coli and eukaryotic initiator tRNAs have
negative determinants, at the same positions, that block their activity
in elongation. The primary negative determinant in E. coli
initiator tRNA is the C1xA72 mismatch at the end of the acceptor stem.
The primary negative determinant in eukaryotic initiator tRNAs is
located in the T C stem, whereas a secondary negative determinant is
the A1:U72 base pair at the end of the acceptor stem. Here we show that
E. coli initiator tRNA also has a secondary negative
determinant for elongation and that it is the U50·G64 wobble base
pair, located at the same position in the T C stem as the primary
negative determinant in eukaryotic initiator tRNAs. Mutation of the
U50·G64 wobble base pair to C50:G64 or U50:A64 base pairs increases
the in vivo amber suppressor activity of initiator tRNA
mutants that have changes in the acceptor stem and in the anticodon
sequence necessary for amber suppressor activity. Binding assays of the
mutant aminoacyl-tRNAs carrying the C50 and A64 changes to the
elongation factor EF-Tu·GTP show marginally higher affinity of the
C50 and A64 mutant tRNAs and increased stability of the
EF-Tu·GTP· aminoacyl-tRNA ternary complexes. Other results show a
large effect of the amino acid attached to a tRNA, glutamine
versus methionine, on the binding affinity toward
EF-Tu·GTP and on the stability of the EF-Tu·GTP·aminoacyl-tRNA ternary complex.
*
This work was supported by Grant R37GM17151 from the
National Institutes of Health.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
Present address: Dept. of Microbiology and Cell Biology, Indian
Institute of Science, Bangalore 560012, India.
§
To whom correspondence should be addressed: Dept. of Biology, Rm.
68-671, Massachusetts Institute of Technology, Cambridge, MA 02139. Tel.: 617-253-4702; Fax: 617-252-1556; E-mail:
bhandary@mit.edu.
Copyright © 2003 by The American Society for Biochemistry and Molecular Biology, Inc.

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
H. Roy and M. Ibba
RNA-dependent lipid remodeling by bacterial multiple peptide resistance factors
PNAS,
March 25, 2008;
105(12):
4667 - 4672.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Ibba and D. Soll
Aminoacyl-tRNAs: setting the limits of the genetic code
Genes & Dev.,
April 1, 2004;
18(7):
731 - 738.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
N. Hino, T. Suzuki, T. Yasukawa, K. Seio, K. Watanabe, and T. Ueda
The pathogenic A4269G mutation in human mitochondrial tRNAIle alters the T-stem structure and decreases the binding affinity for elongation factor Tu
Genes Cells,
March 1, 2004;
9(3):
243 - 252.
[Abstract]
[Full Text]
[PDF]
|
 |
|
Copyright © 2003 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|