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宿主RNA聚合酶对噬菌体SPP1体外转录的限制片段分析。

Restriction fragment analysis of bacteriophage SPP1 in vitro transcription by host RNA polymerase.

作者信息

Chenciner N, Milanesi G

出版信息

J Virol. 1978 Oct;28(1):95-105. doi: 10.1128/JVI.28.1.95-105.1978.

Abstract

In vitro transcription of SPP1 DNA occurred on only one of the two strands, the same which is predominantly transcribed in SPP1-infected cells. Transcripts were distributed in several size classes. Analysis of elongation kinetics and of size distribution, coupled with hybridization to DNA restriction fragments, showed that some regions of the template have more initiation sites than others; some have none. Some regions were transcribed directly, some were transcribed from initiation sites located in other regions, and one was never transcribed. Several transcription initiation sites on SPP1 DNA are located on EcoRI fragment 1; four to five others are distributed among other fragments. Cutting the DNA with EcoRI did not introduce artifactual initiation sites. In vitro transcription units can be localized and oriented with respect to the EcoRI restriction map of SPP1 DNA.

摘要

SPP1 DNA的体外转录仅发生在两条链中的一条上,这与在SPP1感染细胞中主要转录的链相同。转录本分布在几个大小类别中。对延伸动力学和大小分布的分析,以及与DNA限制片段的杂交表明,模板的某些区域比其他区域有更多的起始位点;有些区域没有起始位点。一些区域直接转录,一些区域从位于其他区域的起始位点转录,还有一个区域从未被转录。SPP1 DNA上的几个转录起始位点位于EcoRI片段1上;另外四到五个分布在其他片段中。用EcoRI切割DNA不会引入人为的起始位点。体外转录单位可以相对于SPP1 DNA的EcoRI限制图谱进行定位和定向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d209/354251/aff92024050c/jvirol00202-0107-a.jpg

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