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2
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Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.通过在大肠杆菌中进行DNA融合和克隆分析基因控制信号。
J Mol Biol. 1980 Apr;138(2):179-207. doi: 10.1016/0022-2836(80)90283-1.
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New M13 vectors for cloning.用于克隆的新型M13载体。
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3
Mechanism of insertion and cointegration mediated by IS1 and Tn3.由IS1和Tn3介导的插入和共整合机制。
Cold Spring Harb Symp Quant Biol. 1981;45 Pt 1:283-95. doi: 10.1101/sqb.1981.045.01.041.
4
On the role of IS1 in the formation of hybrids between the bacteriophage P1 and the R plasmid NR1.关于IS1在噬菌体P1与R质粒NR1之间杂种形成中的作用。
Mol Gen Genet. 1980 Jan;177(2):261-70. doi: 10.1007/BF00267437.
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Plasmids containing insertion elements are potential transposons.含有插入元件的质粒是潜在的转座子。
Proc Natl Acad Sci U S A. 1980 Feb;77(2):750-4. doi: 10.1073/pnas.77.2.750.
6
Electroblotting onto activated glass. High efficiency preparation of proteins from analytical sodium dodecyl sulfate-polyacrylamide gels for direct sequence analysis.电转印至活化玻璃上。从分析型十二烷基硫酸钠-聚丙烯酰胺凝胶中高效制备蛋白质用于直接序列分析。
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Rapid and efficient site-specific mutagenesis without phenotypic selection.无需表型选择的快速高效位点特异性诱变。
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Production of single-stranded plasmid DNA.单链质粒DNA的制备。
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Two efficient ribosomal frameshifting events are required for synthesis of mouse mammary tumor virus gag-related polyproteins.合成小鼠乳腺肿瘤病毒gag相关多聚蛋白需要两个有效的核糖体移码事件。
Proc Natl Acad Sci U S A. 1987 Jun;84(12):4298-302. doi: 10.1073/pnas.84.12.4298.
10
Complete nucleotide sequence of a milk-transmitted mouse mammary tumor virus: two frameshift suppression events are required for translation of gag and pol.一种经乳汁传播的小鼠乳腺肿瘤病毒的完整核苷酸序列:gag和pol的翻译需要两个移码抑制事件。
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确定插入序列IS 1编码的转座酶产生所需的翻译移码位点。

Identification of the site of translational frameshifting required for production of the transposase encoded by insertion sequence IS 1.

作者信息

Sekine Y, Nagasawa H, Ohtsubo E

机构信息

Institute of Applied Microbiology, University of Tokyo, Japan.

出版信息

Mol Gen Genet. 1992 Nov;235(2-3):317-24. doi: 10.1007/BF00279376.

DOI:10.1007/BF00279376
PMID:1334529
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7088211/
Abstract

Previous genetic analyses indicated that translational frameshifting in the--1 direction occurs within the run of six adenines in the sequence 5'-TTAAAAAACTC-3' at nucleotide positions 305-315 in IS 1, where the two out-of-phase reading frames insA and B'-insB overlap, to produce transposase with a polypeptide segment Leu-Lys-Lys-Leu at residues 84-87. IS 1 mutants with a 1 bp insertion, which encode mutant transposases with an amino acid substitution within the polypeptide segment at residues 84-87, did not efficiently mediate cointegration, except for an IS 1 mutant which encodes a mutant transposase with a Leu-Arg-Lys-Leu segment instead of Leu-Lys-Lys-Leu. An IS 1 mutant with the DNA segment 5'-CTTAAAAACTC-3' at positions 305-315 carrying the termination codon TAA in the B'-insB reading frame could still mediate cointegration, indicating that codon AAA for Lys corresponding to second, third and fourth positions in the run of adenines is the site of frameshifting. The beta-galactosidase activity specified by several IS 1-lacZ fusion plasmids, in which B'-insB is in-frame with lacZ, showed that the region 292-377 is sufficient for frameshifting. The protein produced by frameshifting from the IS 1-lacZ plasmid in fact contained the polypeptide segment Leu-Lys-Lys-Leu encoded by the DNA segment 5'-TTAAAAAACTC-3', indicating that--1 frameshifting does occur within the run of adenines.

摘要

先前的基因分析表明,在插入序列1(IS 1)中核苷酸位置305 - 315处的5'-TTAAAAAACTC-3'序列的六个腺嘌呤连续排列区域内,会发生-1方向的翻译移码,其中两个不同相位的阅读框insA和B'-insB在此处重叠,从而产生在84 - 87位残基处带有Leu-Lys-Lys-Leu多肽片段的转座酶。具有1 bp插入的IS 1突变体,其编码在84 - 87位残基的多肽片段内有氨基酸替代的突变转座酶,除了一个编码具有Leu-Arg-Lys-Leu片段而非Leu-Lys-Lys-Leu的突变转座酶的IS 1突变体外,均不能有效地介导共整合。在305 - 315位带有DNA片段5'-CTTAAAAACTC-3'且在B'-insB阅读框中带有终止密码子TAA的IS 1突变体仍能介导共整合,这表明与腺嘌呤连续排列中第二、第三和第四位置相对应的赖氨酸密码子AAA是移码位点。几个IS 1-lacZ融合质粒所指定的β-半乳糖苷酶活性(其中B'-insB与lacZ读码框一致)表明,292 - 377区域足以发生移码。实际上,由IS 1-lacZ质粒移码产生的蛋白质包含由DNA片段5'-TTAAAAAACTC-3'编码的Leu-Lys-Lys-Leu多肽片段,这表明在腺嘌呤连续排列区域内确实发生了-1移码。