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大鼠核糖体RNA基因可利用灵长类动物的RNA聚合酶I转录机制:rDNA转录中缺乏绝对的物种特异性。

Rat ribosomal RNA gene can utilize primate RNA polymerase I transcription machinery: lack of absolute species specificity in rDNA transcription.

作者信息

Ghosh A K, Niu H, Jacob S T

机构信息

Department of Pharmacology and Molecular Biology, Chicago Medical School, Illinois 60064, USA.

出版信息

Biochem Biophys Res Commun. 1996 Aug 23;225(3):890-5. doi: 10.1006/bbrc.1996.1268.

Abstract

The transcriptional activity of rodent ribosomal RNA gene (rDNA) in the primate cell was examined in the light of reported species specificity of eukaryotic ribosomal RNA synthesis. The present study showed that rat rDNA can be transcribed in HeLa nuclear extract whereas mouse rDNA was not transcribed in the heterologous extract. Rat and mouse rDNA transcription factors were interchangeable with respect to efficiency and accuracy of transcription. The initiation of rat ribosomal gene transcription by RNA polymerase I occurred at the +1 site in the heterologous extract. Initiation of transcription at the correct site also occurred in vivo following transfection of cloned rat rDNA into the primate (COS-7) cells. These data indicate that rat ribosomal RNA gene can be expressed in the primate system in vitro and in vivo. The absolute lack of species specificity in rDNA transcription has been discussed based on the present data and other reports.

摘要

鉴于已报道的真核生物核糖体RNA合成的物种特异性,对灵长类细胞中啮齿动物核糖体RNA基因(rDNA)的转录活性进行了研究。本研究表明,大鼠rDNA可在HeLa细胞核提取物中进行转录,而小鼠rDNA在异源提取物中则不转录。大鼠和小鼠rDNA转录因子在转录效率和准确性方面是可互换的。RNA聚合酶I对大鼠核糖体基因转录的起始发生在异源提取物中的 +1 位点。将克隆的大鼠rDNA转染到灵长类(COS - 7)细胞后,在体内也会在正确位点发生转录起始。这些数据表明,大鼠核糖体RNA基因可在灵长类系统中进行体外和体内表达。基于本研究数据和其他报道,对rDNA转录中绝对缺乏物种特异性进行了讨论。

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