70S-scanning initiation is a novel and frequent initiation mode of ribosomal translation in bacteria

被引:73
|
作者
Yamamoto, Hiroshi [1 ,2 ]
Wittek, Daniela [1 ]
Gupta, Romi [1 ]
Qin, Bo [1 ,2 ]
Ueda, Takuya [3 ]
Krause, Roland [1 ,4 ]
Yamamoto, Kaori [1 ,2 ]
Albrecht, Renate [1 ,2 ]
Pech, Markus [1 ,5 ]
Nierhaus, Knud H. [1 ,2 ]
机构
[1] Max Planck Inst Mol Genet, Abt Vingron, Ihnestr 73, D-14195 Berlin, Germany
[2] Charite, Inst Med Phys & Biophys, D-10117 Berlin, Germany
[3] Univ Tokyo, Grad Sch Frontier Sci, Dept Med Genome Sci, Kashiwa, Chiba 2778562, Japan
[4] Univ Luxembourg, Luxembourg Ctr Syst Biomed, Campus Belval, L-4362 Esch Belval, Luxembourg
[5] Univ Munich, Dept Biochem, Gene Ctr, D-81377 Munich, Germany
关键词
protein synthesis; ribosomal functions; translational initiation; 30S-binding initiation; 70S-scanning initiation; LEADERLESS MESSENGER-RNAS; AMINOACYL-TRANSFER-RNA; ESCHERICHIA-COLI; PROTEIN-SYNTHESIS; 70S RIBOSOMES; EF-G; FACTOR IF-3; FACTOR IF3; P-SITE; SUBUNIT;
D O I
10.1073/pnas.1524554113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
According to the standard model of bacterial translation initiation, the small ribosomal 30S subunit binds to the initiation site of an mRNA with the help of three initiation factors (IF1-IF3). Here, we describe a novel type of initiation termed "70S-scanning initiation," where the 70S ribosome does not necessarily dissociate after translation of a cistron, but rather scans to the initiation site of the downstream cistron. We detailed the mechanism of 70S-scanning initiation by designing unique monocistronic and polycistronic mRNAs harboring translation reporters, and by reconstituting systems to characterize each distinct mode of initiation. Results show that 70S scanning is triggered by fMet-tRNA and does not require energy; the Shine-Dalgarno sequence is an essential recognition element of the initiation site. IF1 and IF3 requirements for the various initiation modes were assessed by the formation of productive initiation complexes leading to synthesis of active proteins. IF3 is essential and IF1 is highly stimulating for the 70S-scanning mode. The task of IF1 appears to be the prevention of untimely interference by ternary aminoacyl (aa)-tRNA center dot elongation factor thermo unstable (EF-Tu)center dot GTP complexes. Evidence indicates that at least 50% of bacterial initiation events use the 70S-scanning mode, underscoring the relative importance of this translation initiation mechanism.
引用
收藏
页码:E1180 / E1189
页数:10
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