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1
Genetic analysis of the basis of translation in the -1 frame of an unusual non-ORF sequence isolated from phage display.对从噬菌体展示中分离出的一条异常非开放阅读框序列的-1 读框内翻译基础的遗传分析。
Gene Expr. 2002;10(3):109-14.
2
Efficiencies of translation in three reading frames of unusual non-ORF sequences isolated from phage display.从噬菌体展示中分离出的异常非开放阅读框序列在三个阅读框中的翻译效率。
FASEB J. 2000 Mar;14(3):603-11. doi: 10.1096/fasebj.14.3.603.
3
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5
CCC CGA is a weak translational recoding site in Escherichia coli.CCC CGA是大肠杆菌中的一个弱翻译重编码位点。
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6
[Possibility of using fusion proteins for detection of nonsense mutations and frame-shift mutations in BRCA1 gene].[利用融合蛋白检测BRCA1基因无义突变和移码突变的可能性]
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7
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9
Genetic analysis of transfer-related regions of the vancomycin resistance Enterococcus conjugative plasmid pHTbeta: identification of oriT and a putative relaxase gene.耐万古霉素肠球菌接合质粒pHTbeta转移相关区域的遗传分析:oriT和一个假定松弛酶基因的鉴定
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10
The translation of an antiapoptotic protein HIAP2 is regulated by an upstream open reading frame.抗凋亡蛋白HIAP2的翻译受上游开放阅读框调控。
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本文引用的文献

1
Efficiencies of translation in three reading frames of unusual non-ORF sequences isolated from phage display.从噬菌体展示中分离出的异常非开放阅读框序列在三个阅读框中的翻译效率。
FASEB J. 2000 Mar;14(3):603-11. doi: 10.1096/fasebj.14.3.603.
2
Unexpected frameshifts from gene to expressed protein in a phage-displayed peptide library.噬菌体展示肽库中从基因到表达蛋白的意外移码突变。
Proc Natl Acad Sci U S A. 1998 Sep 15;95(19):11146-51. doi: 10.1073/pnas.95.19.11146.
3
Identification of an allosteric binding site on the transcription factor p53 using a phage-displayed peptide library.利用噬菌体展示肽库鉴定转录因子p53上的变构结合位点。
Oncogene. 1998 Apr 16;16(15):1993-9. doi: 10.1038/sj.onc.1201717.
4
Recoding: dynamic reprogramming of translation.重新编码:翻译的动态重编程。
Annu Rev Biochem. 1996;65:741-68. doi: 10.1146/annurev.bi.65.070196.003521.
5
Quantitative analysis of ribosome binding sites in E.coli.大肠杆菌中核糖体结合位点的定量分析。
Nucleic Acids Res. 1994 Apr 11;22(7):1287-95. doi: 10.1093/nar/22.7.1287.
6
Translational reinitiation in the rIIB cistron of bacteriophage T4.噬菌体T4的rIIB顺反子中的翻译重新起始
J Mol Biol. 1981 Jul 5;149(3):433-49. doi: 10.1016/0022-2836(81)90480-0.
7
Translational interference at overlapping reading frames in prokaryotic messenger RNA.原核生物信使核糖核酸中重叠阅读框处的翻译干扰
Gene. 1985;37(1-3):171-9. doi: 10.1016/0378-1119(85)90270-7.
8
Use of tRNA suppressors to probe regulation of Escherichia coli release factor 2.利用tRNA抑制子探究大肠杆菌释放因子2的调控机制。
J Mol Biol. 1988 Sep 5;203(1):75-83. doi: 10.1016/0022-2836(88)90092-7.
9
Errors and alternatives in reading the universal genetic code.通用遗传密码解读中的错误与变体
Microbiol Rev. 1989 Sep;53(3):273-98. doi: 10.1128/mr.53.3.273-298.1989.
10
Translational reinitiation in the presence and absence of a Shine and Dalgarno sequence.存在和不存在夏因-达尔加诺序列时的翻译重新起始
Nucleic Acids Res. 1989 Jul 25;17(14):5501-7. doi: 10.1093/nar/17.14.5501.

对从噬菌体展示中分离出的一条异常非开放阅读框序列的-1 读框内翻译基础的遗传分析。

Genetic analysis of the basis of translation in the -1 frame of an unusual non-ORF sequence isolated from phage display.

作者信息

Zemsky Jennifer, Mandecki Wlodek, Goldman Emanuel

机构信息

Department of Microbiology & Molecular Genetics, New Jersey Medical School, University of Medicine & Dentistry of New Jersey, Newark 07103, USA.

出版信息

Gene Expr. 2002;10(3):109-14.

PMID:12064573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5977510/
Abstract

An unusual peptide-encoding sequence, called H10, and several derivatives of this sequence were previously isolated from a random peptide library screened by phage display during drug discovery protocols. The H10 family of sequences had the unusual property of being expressed despite the absence of an open reading frame. When these sequences were fused to a reporter lacZ gene in all three frames, beta-galactosidase was expressed not only from the parental non-open reading frame, consistent with the original isolations, but also from the frame -1 to the parental. This unexpected translation in a second reading frame could result from either a recoding event or from an internal translation initiation event. In order to elucidate which type of event, a genetic approach was selected to eliminate a potential downstream initiator site within the H10 sequence. This report provides strong evidence that translation in the -1 frame in this family of sequences is indeed originating from a downstream translation initiation event. Unexpectedly, the mutation eliminating the downstream initiation event in the -1 frame simultaneously elevated expression in the original non-open reading frame.

摘要

一种名为H10的不寻常的肽编码序列及其该序列的几种衍生物,先前是在药物发现方案中通过噬菌体展示筛选的随机肽库中分离得到的。H10序列家族具有一种不寻常的特性,即尽管没有开放阅读框也能表达。当这些序列在所有三个阅读框中与报告基因lacZ融合时,β-半乳糖苷酶不仅从亲本非开放阅读框中表达,这与最初的分离结果一致,而且还从亲本的-1阅读框中表达。在第二个阅读框中的这种意外翻译可能是由重编码事件或内部翻译起始事件引起的。为了阐明是哪种类型的事件,选择了一种遗传学方法来消除H10序列内潜在的下游起始位点。本报告提供了有力证据,证明该序列家族中-1阅读框的翻译确实源自下游翻译起始事件。出乎意料的是,消除-1阅读框中下游起始事件的突变同时提高了原始非开放阅读框中的表达。