Constraints on reinitiation of translation in mammals

被引:229
作者
Kozak, M [1 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Biochem, Piscataway, NJ 08854 USA
关键词
D O I
10.1093/nar/29.24.5226
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
The efficiency of reinitiation in mammalian translation systems depends in part on the size and arrangement of upstream open reading frames (upORFs). The gradual decrease in reinitiation as an upORF is lengthened, confirmed here using a variety of sequences, might reflect time-dependent loss of protein factors required for reinitiation. Consistent with the idea that the duration of elongation is what matters, reinitiation was nearly abolished when a pseudoknot that causes a pause in elongation was inserted into a short upORF. Control experiments showed that this transient pause in elongation had little effect on the final protein yield when the pseudoknot was moved from the upORF into the main ORF. Thus, the deleterious effect of slowing elongation is limited to the reinitiation mode. Another aspect of reinitiation investigated here is whether post-termination ribosomes can scan backwards to initiate at AUG codons positioned upstream from the terminator codon. Earlier studies that raised this possibility may have been complicated by the occurrence of leaky scanning along with reinitiation. Re-examination of the question, using constructs that preclude leaky scanning, shows barely detectable reinitiation from an AUG codon positioned 4 nt upstream from the terminator codon and no detectable reinitiation from an AUG codon positioned farther upstream. These experiments carried out with synthetic transcripts help to define the circumstances under which reinitiation may be expected to occur in the growing number of natural mRNAs that deviate from the simple first AUG rule.
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页码:5226 / 5232
页数:7
相关论文
共 55 条
[41]   Complex organisation of the 5′-end of the human glycine tRNA synthetase gene [J].
Mudge, SJ ;
Williams, JH ;
Eyre, HJ ;
Sutherland, GR ;
Cowan, PJ ;
Power, DA .
GENE, 1998, 209 (1-2) :45-50
[42]   Involvement of upstream open reading frames in regulation of rat V1b vasopressin receptor expression [J].
Nomura, A ;
Iwasaki, Y ;
Saito, M ;
Aoki, Y ;
Yamamori, E ;
Ozaki, N ;
Tachikawa, K ;
Mutsuga, N ;
Morishita, M ;
Yoshida, M ;
Asai, M ;
Oiso, Y ;
Saito, H .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 280 (05) :E780-E787
[43]   EFFECT OF UPSTREAM READING FRAMES ON TRANSLATION EFFICIENCY IN SIMIAN VIRUS-40 RECOMBINANTS [J].
PEABODY, DS ;
SUBRAMANI, S ;
BERG, P .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (07) :2704-2711
[44]   SYSTEMIC MOVEMENT OF AN RNA PLANT-VIRUS DETERMINED BY A POINT SUBSTITUTION IN A 5' LEADER SEQUENCE [J].
PETTY, ITD ;
EDWARDS, MC ;
JACKSON, AO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8894-8897
[45]   POSTTRANSCRIPTIONAL MESSENGER-RNA PROCESSING AS A MECHANISM FOR REGULATION OF HUMAN A(1) ADENOSINE RECEPTOR EXPRESSION [J].
REN, HZ ;
STILES, GL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) :4864-4866
[46]   Analysis of capsid formation of human polyomavirus JC (Tokyo-1 strain) by a eukaryotic expression system: Splicing of late RNAs, translation and nuclear transport of major capsid protein VPI, and capsid assembly [J].
Shishido-Hara, Y ;
Hara, Y ;
Larson, T ;
Yasui, K ;
Nagashima, K ;
Stoner, GL .
JOURNAL OF VIROLOGY, 2000, 74 (04) :1840-1853
[47]   RIBOSOMAL PAUSING DURING TRANSLATION OF AN RNA PSEUDOKNOT [J].
SOMOGYI, P ;
JENNER, AJ ;
BRIERLEY, I ;
INGLIS, SC .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (11) :6931-6940
[48]  
Steel LF, 1996, CELL GROWTH DIFFER, V7, P1415
[49]   INTRODUCTION OF HOMOLOGOUS DNA-SEQUENCES INTO MAMMALIAN-CELLS INDUCES MUTATIONS IN THE COGNATE GENE [J].
THOMAS, KR ;
CAPECCHI, MR .
NATURE, 1986, 324 (6092) :34-38
[50]  
Vega Laso Maria R., 1993, Journal of Biological Chemistry, V268, P6453