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在大肠杆菌释放因子2表达过程中真核生物核糖体的移码现象。

Frameshifting by eukaryotic ribosomes during expression of Escherichia coli release factor 2.

作者信息

Donly B C, Tate W P

机构信息

Department of Biochemistry, University of Otago, Dunedin, New Zealand.

出版信息

Proc Biol Sci. 1991 Jun 22;244(1311):207-10. doi: 10.1098/rspb.1991.0072.

DOI:10.1098/rspb.1991.0072
PMID:1679939
Abstract

Normal translation of the gene for E. coli release factor 2 (RF-2) is characterized by a +1 frameshift event that occurs with 30-50% efficiency. Frameshifting on synthetic RF-2 mRNA by eukaryotic ribosomes has also been observed, even though they lack the capability to interact with the frameshift signal in the same manner as prokaryotic ribosomes. We have mutagenized the sequence of the RF-2 gene to eliminate the need for a frameshift, thereby allowing frameshifting efficiency to be measured by direct comparison of RF-2 production from the mutant with production from the wild-type. Measurements using this approach confirm that frameshifting by rabbit reticulocyte lysate ribosomes occurs at the frameshift region, but with a limited efficiency of approximately 0.4%.

摘要

大肠杆菌释放因子2(RF - 2)基因的正常翻译特征是发生+1移码事件,其效率为30 - 50%。即使真核核糖体缺乏与原核核糖体以相同方式与移码信号相互作用的能力,但在合成的RF - 2 mRNA上也观察到了真核核糖体的移码现象。我们对RF - 2基因序列进行了诱变,以消除移码的必要性,从而通过直接比较突变体与野生型的RF - 2产量来测量移码效率。使用这种方法进行的测量证实,兔网织红细胞裂解物核糖体的移码发生在移码区域,但效率有限,约为0.4%。

相似文献

1
Frameshifting by eukaryotic ribosomes during expression of Escherichia coli release factor 2.在大肠杆菌释放因子2表达过程中真核生物核糖体的移码现象。
Proc Biol Sci. 1991 Jun 22;244(1311):207-10. doi: 10.1098/rspb.1991.0072.
2
Frameshifting at the internal stop codon within the mRNA for bacterial release factor-2 on eukaryotic ribosomes.真核生物核糖体上细菌释放因子-2的信使核糖核酸(mRNA)内的内部终止密码子处的移码。
Biochim Biophys Acta. 1990 Aug 27;1050(1-3):283-7. doi: 10.1016/0167-4781(90)90182-2.
3
Frameshifting in the synthesis of Escherichia coli polypeptide chain release factor two on eukaryotic ribosomes.大肠杆菌多肽链释放因子2在真核核糖体上合成时的移码现象。
Eur J Biochem. 1989 Dec 22;186(3):515-21. doi: 10.1111/j.1432-1033.1989.tb15237.x.
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Maintaining the ribosomal reading frame: the influence of the E site during translational regulation of release factor 2.维持核糖体阅读框:E位点在释放因子2翻译调控过程中的影响
Cell. 2004 Jul 9;118(1):45-55. doi: 10.1016/j.cell.2004.06.012.
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Frameshift autoregulation in the gene for Escherichia coli release factor 2: partly functional mutants result in frameshift enhancement.大肠杆菌释放因子2基因中的移码自调控:部分功能性突变体导致移码增强。
Nucleic Acids Res. 1990 Nov 25;18(22):6517-22. doi: 10.1093/nar/18.22.6517.
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Competition between frameshifting, termination and suppression at the frameshift site in the Escherichia coli release factor-2 mRNA.大肠杆菌释放因子-2 mRNA移码位点处移码、终止和抑制之间的竞争。
Nucleic Acids Res. 1993 Nov 11;21(22):5074-8. doi: 10.1093/nar/21.22.5074.
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Increased ribosomal accuracy increases a programmed translational frameshift in Escherichia coli.核糖体准确性的提高会增加大肠杆菌中一种程序性翻译移码。
Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2315-9. doi: 10.1073/pnas.90.6.2315.
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Genetic analysis of the E site during RF2 programmed frameshifting.在RF2介导的程序性移码过程中E位点的遗传分析。
RNA. 2007 Sep;13(9):1483-91. doi: 10.1261/rna.638707. Epub 2007 Jul 27.
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A ribosomal frameshifting error during translation of the argI mRNA of Escherichia coli.大肠杆菌argI信使核糖核酸(mRNA)翻译过程中的核糖体移码错误。
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rRNA-mRNA base pairing stimulates a programmed -1 ribosomal frameshift.核糖体RNA-信使核糖核酸碱基配对刺激程序性-1核糖体移码。
J Bacteriol. 1994 Nov;176(22):6842-51. doi: 10.1128/jb.176.22.6842-6851.1994.

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