THE IMMEDIATE DOWNSTREAM CODON STRONGLY INFLUENCES THE EFFICIENCY OF UTILIZATION OF EUKARYOTIC TRANSLATION INITIATION CODONS

被引:102
作者
GRUNERT, S [1 ]
JACKSON, RJ [1 ]
机构
[1] UNIV CAMBRIDGE,DEPT BIOCHEM,CAMBRIDGE CB2 1QW,ENGLAND
基金
英国惠康基金;
关键词
INITIATION CODON CONTEXT; NON-AUG INITIATION CODONS; SCANNING RIBOSOME MODEL; TRANSLATION INITIATION;
D O I
10.1002/j.1460-2075.1994.tb06669.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nucleotide substitutions were introduced into the initiation site of an influenza virus NS cDNA derivative at the +4, +5 and +6 positions (where the A of the AUG codon is defined as +1), in the background of either AUG or CUG as the initiation codon. Capped transcripts of these constructs were translated in rabbit reticulocyte lysate under conditions where the selection of initiation sites conformed to the scanning ribosome model. With CUG as the initiation codon, the efficiency of initiation was as strongly influenced by the nature of the residue in the +5 position as at +4, whilst the influence of the +6 position was smaller, The residues favourable to initiation were as follows: at +4, only G was stimulatory; at +5, A was strongly stimulatory acid C fairly beneficial; and at +6, only U exerted any positive influence. The positive influence of the favourable residues (or the negative influence of unfavourable residues) at each position appeared to be additive. With AUG as the initiation codon, the pattern of response to mutations in the +4 and +5 positions was qualitatively similar, but the quantitative effects were smaller. Thus the optimum downstream context for initiation is A/CUGGAU.
引用
收藏
页码:3618 / 3630
页数:13
相关论文
共 33 条
[1]   SUBCELLULAR FATE OF THE INT-2 ONCOPROTEIN IS DETERMINED BY CHOICE OF INITIATION CODON [J].
ACLAND, P ;
DIXON, M ;
PETERS, G ;
DICKSON, C .
NATURE, 1990, 343 (6259) :662-665
[2]   INVIVO HALF-LIFE OF A PROTEIN IS A FUNCTION OF ITS AMINO-TERMINAL RESIDUE [J].
BACHMAIR, A ;
FINLEY, D ;
VARSHAVSKY, A .
SCIENCE, 1986, 234 (4773) :179-186
[3]   DIRECT MAPPING OF ADENO-ASSOCIATED VIRUS CAPSID PROTEIN-B AND PROTEIN-C - A POSSIBLE ACG INITIATION CODON [J].
BECERRA, SP ;
ROSE, JA ;
HARDY, M ;
BAROUDY, BM ;
ANDERSON, CW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (23) :7919-7923
[4]  
BOCK R, 1994, EMBO J, V13, P3608
[5]   THE PARAINFLUENZA VIRUS TYPE-1 P/C GENE USES A VERY EFFICIENT GUG CODON TO START ITS C'-PROTEIN [J].
BOECK, R ;
CURRAN, J ;
MATSUOKA, Y ;
COMPANS, R ;
KOLAKOFSKY, D .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1765-1768
[6]   EUKARYOTIC START AND STOP TRANSLATION SITES [J].
CAVENER, DR ;
RAY, SC .
NUCLEIC ACIDS RESEARCH, 1991, 19 (12) :3185-3192
[7]  
CIGAN AM, 1987, GENE, V59, P1
[8]   RIBOSOMAL INITIATION FROM AN ACG CODON IN THE SENDAI VIRUS P/C MESSENGER-RNA [J].
CURRAN, J ;
KOLAKOFSKY, D .
EMBO JOURNAL, 1988, 7 (01) :245-251
[9]   EFFICIENT INITIATION OF MAMMALIAN MESSENGER-RNA TRANSLATION AT A CUG CODON [J].
DASSO, MC ;
JACKSON, RJ .
NUCLEIC ACIDS RESEARCH, 1989, 17 (16) :6485-6497
[10]   ON THE FIDELITY OF MESSENGER-RNA TRANSLATION IN THE NUCLEASE-TREATED RABBIT RETICULOCYTE LYSATE SYSTEM [J].
DASSO, MC ;
JACKSON, RJ .
NUCLEIC ACIDS RESEARCH, 1989, 17 (08) :3129-3144