首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Nucleotide sequence of the primary origin of bacteriophage T7 DNA replication: relationship to adjacent genes and regulatory elements.
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Nucleotide sequence of the primary origin of bacteriophage T7 DNA replication: relationship to adjacent genes and regulatory elements.

机译:T7 DNA噬菌体复制的主要起点的核苷酸序列:与相邻基因和调控元件的关系。

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摘要

The 682-base-pair nucleotide sequence between positions 14.45 and 16.15 on the bacteriophage T7 DNA molecule has been determined. We can identify not only the sequence of the primary origin of DNA replication but also the termination of gene 1, all of genes 1.1 and 1.2, the start of gene 1.3, and a number of regulatory sequences. The endpoints of four deletion mutations that extend into this region have been determined. These mutations are inferred to have arisen by recombination between short homologous sequences, three of which ar T7 RNA polymerase promoters. The base changes of four point mutations in gene 1.2 have been identified. The sequence essential for initiation at the primary origin is located between the left endpoints of the two deletions D2 and D303. Sequence analysis of these mutants assigns the primary origin to a 129-base-pair segment between positions 14.73 and 15.05. This intergenic segment is A+T-rich (75%) and contains a single T7 gene 4 protein recognition site; it is preceded by two tandem T7 RNA polymerase promoters. A model for initiation of T7 DNA replication is presented.
机译:已经确定了噬菌体T7 DNA分子上14.45和16.15位之间的682个碱基对的核苷酸序列。我们不仅可以识别DNA复制的主要来源的序列,还可以识别基因1,所有基因1.1和1.2的终止,基因1.3的起始以及许多调控序列。已经确定了延伸到该区域的四个缺失突变的终点。推测这些突变是由于短同源序列之间的重组引起的,其中三个同源序列是T7 RNA聚合酶启动子。已经确定了基因1.2中四个点突变的碱基变化。在主要起始点起始所必需的序列位于两个缺失D2和D303的左端点之间。这些突变体的序列分析将主要来源指定为位置14.73和15.05之间的129个碱基对片段。这个基因间片段富含A + T(75%),并包含单个T7基因4蛋白识别位点;它之前有两个串联的T7 RNA聚合酶启动子。提出了启动T7 DNA复制的模型。

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