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线粒体DNA充当杆状病毒RNA聚合酶的潜在启动子。

Mitochondrial DNA acts as potential promoter of the baculovirus RNA polymerase.

作者信息

Mans R M, Knebel-Mörsdorf D

机构信息

Institute of Genetics, University of Cologne, Germany.

出版信息

Biol Chem. 1999 May;380(5):579-83. doi: 10.1515/BC.1999.073.

Abstract

We have examined whether mitochondrial DNA could act as target of the RNA polymerase encoded by the baculovirus Autographa californica multicapsid nuclear polyhedrosis virus, because the baculovirus late promoters and the control region of host mitochondrial DNA show a high degree of sequence similarity. In vitro transcription using mitochondrial DNA from Spodoptera frugiperda cells and nuclear extracts prepared from baculovirus infected cells demonstrates that mitochondrial DNA is recognized by the viral RNA polymerase. Transcriptional initiation occurs at TAAG sequences, although not all of the six TAAG motifs present in the mitochondrial DNA fragment are recognized. The TAAG motif in the control region served as weak transcriptional start site, but some of the TAAG motifs in the coding sequences of the adjacent tRNA and rRNA genes are recognized efficiently. The sequences flanking the TAAG motifs used as transcriptional start sites have a lower helix stability than the flanking sequences of the nonfunctional TAAG motifs. These results support the view that helix stability rather than sequence specificity is an important factor for recognition of TAAG motifs by the viral RNA polymerase.

摘要

我们研究了线粒体DNA是否可作为苜蓿银纹夜蛾多粒包埋核型多角体病毒编码的RNA聚合酶的作用靶点,因为杆状病毒晚期启动子与宿主线粒体DNA的控制区显示出高度的序列相似性。使用草地贪夜蛾细胞的线粒体DNA和杆状病毒感染细胞制备的核提取物进行体外转录,结果表明线粒体DNA可被病毒RNA聚合酶识别。转录起始于TAAG序列,尽管线粒体DNA片段中存在的六个TAAG基序并非全部被识别。控制区中的TAAG基序作为较弱的转录起始位点,但相邻tRNA和rRNA基因编码序列中的一些TAAG基序能被有效识别。用作转录起始位点的TAAG基序两侧的序列,其螺旋稳定性低于无功能TAAG基序两侧的序列。这些结果支持了这样一种观点,即螺旋稳定性而非序列特异性是病毒RNA聚合酶识别TAAG基序的重要因素。

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