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转录方向在体外系统中会影响λ噬菌体的复制模式。

Direction of transcription affects the replication mode of lambda in an in vitro system.

作者信息

Kouhara H, Tsurimoto T, Matsubara K

机构信息

Institute for Molecular and Cellular Biology, Osaka University Yamada-oka, Japan.

出版信息

Mol Gen Genet. 1987 Jul;208(3):428-35. doi: 10.1007/BF00328134.

Abstract

A set of artificial circular plasmids, named plasmoids, was constructed. They are about 1 kb in size and consist of a 178 bp lambda dv minimal DNA replication origin (ori) which has four direct repeats and the A + T-rich region conferring polarity to the ori fragment, a 775 bp DNA segment that codes for the CAT amino acid sequence and the 99 bp lac promoter (plac). They carry no other functional genes or genetic sites. The constructions involved various combinations of relative orientations of these components. These molecules do not replicate in vivo because they lack genes coding for initiation proteins, but they do replicate in an in vitro system (Fuller et al. 1981), and can be used for studies of interactions between transcription and replication. In these plasmids, major transcription starts from the strong plac, and some weak unscheduled transcription starts from several other initiation sites. The major RNA synthesis was found to interfere with the unscheduled RNA synthesis, which was occurring on the opposite strand. The most active replication took place when the major RNA synthesis went through the lambda origin region in the direction which occurs naturally in the lambda genome. Under these conditions, DNA synthesis going against such transcription was less than that going along with the major transcription. When RNA synthesis through the lambda origin region was in the opposite direction, DNA synthesis in the same direction was about half of that observed in the above case, whereas that going against transcription was very weak.

摘要

构建了一组人工环状质粒,命名为类质粒。它们大小约为1 kb,由一个178 bp的λdv最小DNA复制起点(ori)组成,该起点有四个直接重复序列以及赋予ori片段极性的富含A + T的区域,一个编码CAT氨基酸序列的775 bp DNA片段和99 bp的乳糖启动子(plac)。它们不携带其他功能基因或遗传位点。构建过程涉及这些组件相对方向的各种组合。这些分子在体内不复制,因为它们缺乏编码起始蛋白的基因,但它们在体外系统中可以复制(富勒等人,1981年),可用于研究转录与复制之间的相互作用。在这些质粒中,主要转录从强plac开始,一些弱的非计划转录从其他几个起始位点开始。发现主要RNA合成会干扰在相反链上发生的非计划RNA合成。当主要RNA合成以在λ基因组中自然发生的方向穿过λ起点区域时,发生最活跃的复制。在这些条件下,与这种转录相反方向的DNA合成少于与主要转录同向的DNA合成。当通过λ起点区域的RNA合成方向相反时,相同方向的DNA合成约为上述情况的一半,而与转录相反方向的DNA合成非常弱。

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