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噬菌体SP6特异性RNA聚合酶。II. SP6 DNA的图谱绘制及体外选择性转录

Bacteriophage SP6-specific RNA polymerase. II. Mapping of SP6 DNA and selective in vitro transcription.

作者信息

Kassavetis G A, Butler E T, Roulland D, Chamberlin M J

出版信息

J Biol Chem. 1982 May 25;257(10):5779-88.

PMID:6279614
Abstract

DNA from bacteriophage SP6 grown on Salmonella typhimurium LT2 is a linear duplex with a unique DNA sequence having a molecular weight of 2.9 x 10(6) (43.500 base pairs). Restriction endonuclease cleavage maps on SP6 DNA for Ava II, Kpn I, Bgl II, Eco RI, and HindIII have been determined. SP6 DNA is transcribed selectively in vitro by Escherichia coli RNA polymerase, predominantly from three strong promoter sites located near the left end of the standard physical map, reading rightward to a termination site near 6,000 base pairs. Transcription in vitro by purified SP6-specific RNA polymerase gives rise to at least 10 discrete RNA species, all of which are read rightward. Promoter sites for these species are located throughout the rightmost 90% of the SP6 DNA molecule, although precise mapping has not yet been carried out. The general form of the SP6 transcriptional map is similar to the T7- and T3-like phages, although no gross sequence homologies are evident from DNA-RNA hybridization experiments.

摘要

在鼠伤寒沙门氏菌LT2上生长的噬菌体SP6的DNA是一种线性双链体,具有独特的DNA序列,分子量为2.9×10⁶(43,500个碱基对)。已经确定了Ava II、Kpn I、Bgl II、Eco RI和HindIII在SP6 DNA上的限制性内切酶切割图谱。SP6 DNA在体外被大肠杆菌RNA聚合酶选择性转录,主要从标准物理图谱左端附近的三个强启动子位点开始,向右转录至6000个碱基对附近的终止位点。用纯化的SP6特异性RNA聚合酶在体外进行转录会产生至少10种不同的RNA种类,所有这些RNA都是向右转录的。这些种类的启动子位点位于SP6 DNA分子最右侧的90%区域内,尽管尚未进行精确的图谱绘制。尽管从DNA-RNA杂交实验中没有明显的总体序列同源性,但SP6转录图谱的一般形式与T7和T3样噬菌体相似。

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