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结核放线菌素类抗生素对粗糙脉孢菌VS核酶切割的增强作用。

Enhancement of Neurospora VS ribozyme cleavage by tuberactinomycin antibiotics.

作者信息

Olive J E, De Abreu D M, Rastogi T, Andersen A A, Mittermaier A K, Beattie T L, Collins R A

机构信息

Canadian Institute for Advanced Research Program in Evolutionary Biology, Department of Molecular and Medical Genetics, University of Toronto, Ontario.

出版信息

EMBO J. 1995 Jul 3;14(13):3247-51. doi: 10.1002/j.1460-2075.1995.tb07327.x.

DOI:10.1002/j.1460-2075.1995.tb07327.x
PMID:7621836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC394386/
Abstract

Several examples of inhibition of the function of a ribozyme or RNA-protein complex have shown that certain antibiotics can interact specifically with RNA. There are, however, few examples of antibiotics that have a positive, rather than a negative, effect on the function of an RNA. We have found that micromolar concentrations of viomycin, a basic, cyclic peptide antibiotic of the tuberactinomycin group, enhance the cleavage of a ribozyme derived from Neurospora VS RNA. Viomycin decreases by an order of magnitude the concentration of magnesium required for cleavage. It also stimulates an otherwise insignificant transcleavage reaction by enhancing interactions between RNA molecules. The ability of viomycin to enhance some RNA-mediated reactions but inhibit others, including translation and Group I intron splicing, demonstrates the potential for natural selection by small molecules during evolution in the 'RNA world' and may have broader implications with respect to ribozyme expression and activity in contemporary cells.

摘要

对核酶或RNA - 蛋白质复合物功能抑制的几个例子表明,某些抗生素可以与RNA特异性相互作用。然而,对抗生素对RNA功能有积极而非消极影响的例子却很少。我们发现,微摩尔浓度的紫霉素(一种属于结核放线菌素组的碱性环状肽抗生素)能增强源自粗糙脉孢菌VS RNA的核酶的切割作用。紫霉素使切割所需的镁离子浓度降低了一个数量级。它还通过增强RNA分子之间的相互作用来刺激原本不显著的反式切割反应。紫霉素增强一些RNA介导的反应但抑制其他反应(包括翻译和I组内含子剪接)的能力,证明了在“RNA世界”进化过程中小分子进行自然选择的潜力,并且可能对当代细胞中核酶的表达和活性具有更广泛的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/0f0dbc70cd13/emboj00037-0292-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/1a2d3fafb9bb/emboj00037-0290-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/aba4c75c3393/emboj00037-0291-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/0f0dbc70cd13/emboj00037-0292-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/1a2d3fafb9bb/emboj00037-0290-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/aba4c75c3393/emboj00037-0291-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbfd/394386/0f0dbc70cd13/emboj00037-0292-a.jpg

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本文引用的文献

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Footprinting the sites of interaction of antibiotics with catalytic group I intron RNA.确定抗生素与I类催化内含子RNA相互作用位点
Science. 1993 Jun 4;260(5113):1500-3. doi: 10.1126/science.8502993.
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Splice-site selection and decoding: are they related?剪接位点选择与解码:它们相关吗?
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Orig Life Evol Biosph. 1999 Aug;29(4):391-404. doi: 10.1023/a:1006572028643.
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Self-cleavage activity of the genomic HDV ribozyme in the presence of various divalent metal ions.基因组丁型肝炎病毒核酶在各种二价金属离子存在下的自我切割活性。
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Optimization of an anti-HIV hairpin ribozyme by in vitro selection.通过体外筛选优化抗HIV发夹状核酶
J Biol Chem. 1993 Nov 25;268(33):24515-8.
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An RNA chaperone activity of non-specific RNA binding proteins in hammerhead ribozyme catalysis.锤头状核酶催化中非特异性RNA结合蛋白的RNA伴侣活性。
EMBO J. 1994 Jun 15;13(12):2913-24. doi: 10.1002/j.1460-2075.1994.tb06586.x.
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Facilitation of hammerhead ribozyme catalysis by the nucleocapsid protein of HIV-1 and the heterogeneous nuclear ribonucleoprotein A1.
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