An AUG initiation codon, not codon-anticodon complementarity, is required for the translation of unleadered mRNA in Escherichia coli

被引:62
作者
Van Etten, WJ [1 ]
Janssen, GR [1 ]
机构
[1] Miami Univ, Dept Microbiol, Oxford, OH 45056 USA
关键词
D O I
10.1046/j.1365-2958.1998.00744.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
We determined the in vivo translational efficiency of 'unleadered' lacZ compared with a conventionally leadered lacZ with and without a Shine-Dalgarno (SD) sequence in Escherichia coli and found that changing the SD sequence of leadered lacZ from the consensus 5'-AGGA-3' to 5'-UUUU-3' results in a 15-fold reduction in translational efficiency; however, removing the leader altogether results in only a twofold reduction. An increase in translation coincident with the removal of the leader lacking a SD sequence suggests the existence of stronger or novel translational signals within the coding sequence in the absence of the leader. We examined, therefore, a change in the translational signals provided by altering the AUG initiation codon to other naturally occurring initiation codons (GUG, UUG, CUG) in the presence and absence of a leader and find that mRNAs lacking leader sequences are dependent upon an AUG initiation codon, whereas leadered mRNAs are not. This suggests that mRNAs lacking leader sequences are either more dependent on perfect codon-anticodon complementarity or require an AUG initiation codon in a sequence-specific manner to form productive initiation complexes. A mutant initiator tRNA with compensating anticodon mutations restored expression of leadered, but not unleadered, mRNAs with UAG start codons, indicating that codon-anticodon complementarity was insufficient for the translation of mRNA lacking leader sequences. These data suggest that a cognate AUG initiation codon specifically serves as a stronger and different translational signal in the absence of an untranslated leader.
引用
收藏
页码:987 / 1001
页数:15
相关论文
共 54 条
[1]   UNUSUAL RIBOSOME BINDING-PROPERTIES OF MESSENGER-RNA ENCODING BACTERIOPHAGE-LAMBDA REPRESSOR [J].
BALAKIN, AG ;
SKRIPKIN, EA ;
SHATSKY, IN ;
BOGDANOV, AA .
NUCLEIC ACIDS RESEARCH, 1992, 20 (03) :563-571
[2]   THE MESSENGER-RNA FOR THE 23S RIBOSOMAL-RNA METHYLASE ENCODED BY THE ERME GENE OF SACCHAROPOLYSPORA-ERYTHRAEA IS TRANSLATED IN THE ABSENCE OF A CONVENTIONAL RIBOSOME-BINDING SITE [J].
BIBB, MJ ;
WHITE, J ;
WARD, JM ;
JANSSEN, GR .
MOLECULAR MICROBIOLOGY, 1994, 14 (03) :533-545
[3]   RIBOSOME-MESSENGER RECOGNITION - MESSENGER-RNA TARGET SITES FOR RIBOSOMAL-PROTEIN S1 [J].
BONI, IV ;
ISAEVA, DM ;
MUSYCHENKO, ML ;
TZAREVA, NV .
NUCLEIC ACIDS RESEARCH, 1991, 19 (01) :155-162
[4]   AN ARCHAEBACTERIAL RNA-POLYMERASE BINDING-SITE AND TRANSCRIPTION INITIATION OF THE HISA GENE IN METHANOCOCCUS-VANNIELII [J].
BROWN, JW ;
THOMM, M ;
BECKLER, GS ;
FREY, G ;
STETTER, KO ;
REEVE, JN .
NUCLEIC ACIDS RESEARCH, 1988, 16 (01) :135-150
[5]  
Childs J., 1985, SEQUENCE SPECIFICITY, P341
[6]   SITE-DIRECTED MUTAGENESIS OF VIRTUALLY ANY PLASMID BY ELIMINATING A UNIQUE SITE [J].
DENG, WP ;
NICKOLOFF, JA .
ANALYTICAL BIOCHEMISTRY, 1992, 200 (01) :81-88
[7]   POSTTRANSCRIPTIONAL REGULATORY MECHANISMS IN ESCHERICHIA-COLI [J].
GOLD, L .
ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 :199-233
[8]   INITIATION OF MESSENGER-RNA TRANSLATION IN PROKARYOTES [J].
GUALERZI, CO ;
PON, CL .
BIOCHEMISTRY, 1990, 29 (25) :5881-5889
[9]   DOMAINS OF INITIATOR TRANSFER-RNA AND INITIATION CODON CRUCIAL FOR INITIATOR TRANSFER-RNA SELECTION BY ESCHERICHIA-COLI IF3 [J].
HARTZ, D ;
BINKLEY, J ;
HOLLINGSWORTH, T ;
GOLD, L .
GENES & DEVELOPMENT, 1990, 4 (10) :1790-1800
[10]  
HOSHIKO S, 1988, GENE, V68, P285