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大肠杆菌乳糖阻遏蛋白mRNA的5′末端核苷酸序列:翻译起始和重新起始位点的特征

5'-Terminal nucleotide sequence of Escherichia coli lactose repressor mRNA: features of translational initiation and reinitiation sites.

作者信息

Steege D A

出版信息

Proc Natl Acad Sci U S A. 1977 Oct;74(10):4163-7. doi: 10.1073/pnas.74.10.4163.

Abstract

In a sequence of 214 nucleotides at the 5' terminus of the I gene mRNA, which codes for the lactose repressor protein of Escherichia coli, (i) an untranslated leader sequence of 28 residues precedes the repressor coding region; (ii) a GUG initiates synthesis of the wild-type repressor; (iii) GUG and AUG are the functional initiators for the synthesis of restart polypeptides activated by early I gene amber mutations, confirming previous assignments for these residues based on protein sequencing data; and (iv) sequences complementary to 16S ribosomal RNA provide stronger potential mRNA.16S rRNA interaction at the wild-type initiation site than at the restart sites. When I mRNA is used to direct the formation of initiation complexes in vitro, ribosomes bind only to the wild-type initiator region.A striking feature of the I mRNA sequence is the presence of a number of in-phase GUGs that have not been observed to serve as initiation signals in vivo in the nonsense mutant strains examined. The selective use of potential initiator triplets in the I mRNA leads to the following conclusions. First, when presented with several neighboring initiator triplets at the wild-type initiator region, ribosomes select the one preceded by the strongest appropriately positioned complementarity to the 16S 3' end. Second, ribosomes do not restart after termination simply by moving to the next available initiator codon. Third, the formation of stable secondary structures predicted for the untranslated I mRNA beyond chain-terminating nonsense mutations may prevent ribosome access to some potential reinitiation sites.

摘要

在编码大肠杆菌乳糖阻遏蛋白的I基因mRNA的5'末端的214个核苷酸序列中,(i)在阻遏蛋白编码区之前有一个28个残基的非翻译前导序列;(ii)一个GUG起始野生型阻遏蛋白的合成;(iii)GUG和AUG是由早期I基因琥珀突变激活的重新起始多肽合成的功能性起始密码子,这证实了基于蛋白质测序数据对这些残基的先前归属;(iv)与16S核糖体RNA互补的序列在野生型起始位点比在重新起始位点提供更强的潜在mRNA-16S rRNA相互作用。当I mRNA用于体外指导起始复合物的形成时,核糖体仅结合到野生型起始区域。I mRNA序列的一个显著特征是存在许多同相位的GUG,在所检测的无义突变菌株中,尚未观察到它们在体内作为起始信号。I mRNA中潜在起始三联体的选择性使用导致以下结论。首先,当在野生型起始区域出现几个相邻的起始三联体时,核糖体选择与16S 3'末端具有最强适当定位互补性的那个三联体之前的三联体。其次,核糖体在终止后不会简单地通过移动到下一个可用的起始密码子来重新起始。第三,预测在链终止无义突变之后的未翻译I mRNA形成的稳定二级结构可能会阻止核糖体接近一些潜在的重新起始位点。

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