Initiation of translation in prokaryotes and eukaryotes

被引:1122
作者
Kozak, M [1 ]
机构
[1] Univ Med & Dent New Jersey, Dept Biochem, Piscataway, NJ 08854 USA
关键词
messenger RNA; protein synthesis; ribosome; scanning model; translation initiation factors;
D O I
10.1016/S0378-1119(99)00210-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mechanisms whereby ribosomes engage a messenger RNA and select the start site for translation differ between prokaryotes and eukaryotes. Initiation sites in polycistronic prokaryotic mRNAs are usually selected via base pairing with ribosomal RNA. That straightforward mechanism is made complicated and interesting by cis- and trans-acting elements employed to regulate translation. Initiation sites in eukaryotic mRNAs are reached via a scanning mechanism which predicts that translation should start at the AUG codon nearest the 5' end of the mRNA. Interest has focused on mechanisms that occasionally allow escape from this first AUG rule. With natural mRNAs, three escape mechanisms - context-dependent leaky scanning, reinitiation; and possibly direct internal initiation - allow access to AUG codons which, although not first, are still close to the 5' end of the mRNA. This constraint on the initiation step of translation in eukaryotes dictates the location of transcriptional promoters and may have contributed to the evolution of splicing. The binding of Met-tRNA to ribosomes is mediated by a GTP-binding protein in both prokaryotes and eukaryotes, but the more complex structure of the eukaryotic factor (eIF-2) and its association with other proteins underlie some aspects of initiation unique to eukaryotes. Modulation of GTP hydrolysis by eIF-2 is important during the scanning phase of initiation, while modulating the release of GDP from eIF-2 is a key mechanism for regulating translation in eukaryotes. Our understanding of how some other protein factors participate in the initiation phase of translation is in flux. Genetic tests suggest that some proteins conventionally counted as eukaryotic initiation factors may not be required for translation, while other tests have uncovered interesting new candidates. Some popular ideas about the initiation pathway are predicated on static interactions between isolated factors and mRNA, The need for functional testing of these complexes is discussed. Interspersed with these theoretical topics are some practical points concerning the interpretation of cDNA sequences and the use of in vitro translation systems. Some human diseases resulting from defects in the initiation step of translation are also discussed. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 208
页数:22
相关论文
共 260 条
[41]   TRANSFER RNA(IMET) FUNCTIONS IN DIRECTING THE SCANNING RIBOSOME TO THE START SITE OF TRANSLATION [J].
CIGAN, AM ;
FENG, L ;
DONAHUE, TF .
SCIENCE, 1988, 242 (4875) :93-97
[42]   MUTATIONAL ANALYSIS OF THE HIS4 TRANSLATIONAL INITIATOR REGION IN SACCHAROMYCES-CEREVISIAE [J].
CIGAN, AM ;
PABICH, EK ;
DONAHUE, TF .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (07) :2964-2975
[43]   PHOSPHORYLATION INHIBITS GUANINE-NUCLEOTIDE EXCHANGE ON EUKARYOTIC INITIATION FACTOR-II [J].
CLEMENS, MJ ;
PAIN, VM ;
WONG, ST ;
HENSHAW, EC .
NATURE, 1982, 296 (5852) :93-95
[44]   The double-stranded RNA-dependent protein kinase PKR: Structure and function [J].
Clemens, MJ ;
Elia, A .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1997, 17 (09) :503-524
[45]   Molecular cloning, chromosomal mapping, and characterization of the mouse UDP-galactose:ceramide galactosyltransferase gene [J].
Coetzee, T ;
Li, X ;
Fujita, N ;
Marcus, J ;
Suzuki, K ;
Francke, U ;
Popko, B .
GENOMICS, 1996, 35 (01) :215-222
[46]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[47]   mRNA stabilization by poly(A) binding protein is independent of poly(A) and requires translation [J].
Coller, JM ;
Gray, NK ;
Wickens, MP .
GENES & DEVELOPMENT, 1998, 12 (20) :3226-3235
[48]   Indirect regulation of translational termination efficiency at highly expressed genes and recoding sites by the factor recycling function of Escherichia coli release factor RF3 [J].
Crawford, DJG ;
Ito, K ;
Nakamura, Y ;
Tate, WP .
EMBO JOURNAL, 1999, 18 (03) :727-732
[49]   MOLECULAR AND FUNCTIONAL-ANALYSIS OF A LYMPHOCYTE CHEMOATTRACTANT FACTOR - ASSOCIATION OF BIOLOGIC FUNCTION WITH CD4 EXPRESSION [J].
CRUIKSHANK, WW ;
CENTER, DM ;
NISAR, N ;
WU, MN ;
NATKE, B ;
THEODORE, AC ;
KORNFELD, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) :5109-5113
[50]  
Cuddihy AR, 1999, MOL CELL BIOL, V19, P2475