Hartz D, McPheeters D S, Gold L
Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, 80309-0347.
J Mol Biol. 1991 Mar 5;218(1):83-97. doi: 10.1016/0022-2836(91)90875-7.
We have studied the classic initiation elements of mRNA sequence and structure to better understand their influence on translation initiation rates in Escherichia coli. Changes introduced in the initiation codon, the Shine and Dalgarno sequence, the spacing between those two elements, and in the secondary structures within initiation domains each change the rate of 30 S ternary complex formation. We measured these differences using extension inhibition analysis, a technique we have called "toeprinting". The rate of 30 S initiation complex formation in the absence of initiation factors agrees well with in vivo translation rates in some instances, although in others a regulatory role of initiation factors in 30 S complex formation is likely. Nucleotides 5' to the Shine and Dalgarno domain facilitate ternary complex formation.
我们研究了mRNA序列和结构的经典起始元件,以更好地理解它们对大肠杆菌翻译起始速率的影响。起始密码子、Shine和Dalgarno序列、这两个元件之间的间距以及起始结构域内二级结构的变化,均会改变30S三元复合物的形成速率。我们使用延伸抑制分析(一种我们称为“足迹法”的技术)来测量这些差异。在某些情况下,缺乏起始因子时30S起始复合物的形成速率与体内翻译速率非常吻合,尽管在其他情况下,起始因子在30S复合物形成中可能具有调节作用。Shine和Dalgarno结构域5'端的核苷酸促进三元复合物的形成。