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通过核延伸实验激活暂停的RNA聚合酶。

Activation of pausing RNA polymerases by nuclear run-on experiments.

作者信息

Eick D, Kohlhuber F, Wolf D A, Strobl L J

机构信息

Institut für Klinische Molekularbiologie und Tumorgenetik, Forschungszentrum für Umwelt und Gesundheit, Munich, Germany.

出版信息

Anal Biochem. 1994 May 1;218(2):347-51. doi: 10.1006/abio.1994.1190.

Abstract

The nuclear run-on transcription assay is the only approach to measure the transcriptional activity of a given gene in its genuine structural and regulatory cellular context. However, serious problems in the interpretation of results can arise from the artificial activation of paused RNA polymerases during the transcription reaction, leading to false results with regard to the level and mode of gene regulation in vivo. We have used the example of the human proto-oncogene c-myc, which has previously been reported to be regulated by premature termination of transcription, to describe the problems and pitfalls in the interpretation of nuclear run-on experiments. We show here that activation of paused, elongation-incompetent polymerases in nuclear run-on experiments produces a strong transcription signal on c-myc exon 1 in cells which do not express c-myc steady-state RNA.

摘要

核转录分析是在基因真正的结构和细胞调节背景下测量给定基因转录活性的唯一方法。然而,转录反应过程中暂停的RNA聚合酶的人工激活可能会导致结果解释出现严重问题,从而在体内基因调控水平和模式方面产生错误结果。我们以人类原癌基因c-myc为例(此前有报道称该基因受转录提前终止调控),来描述核转录实验结果解释中的问题和陷阱。我们在此表明,核转录实验中暂停的、无延伸能力的聚合酶的激活,在不表达c-myc稳态RNA的细胞中,会在c-myc外显子1上产生强烈的转录信号。

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