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Template recognition sequence for RNA primer synthesis by gene 4 protein of bacteriophage T7.

机译:T7基因4蛋白合成RNA引物的模板识别序列。

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摘要

The gene 4 protein of bacteriophage T7 recognizes specific sequences on single-stranded DNA and then catalyzes the synthesis of tetraribonucleotide primers complementary to the template. With phi X174 DNA as a template, the gene 4 protein enables T7 DNA polymerase (deoxynucleosidetriphosphate:DNA deoxynucleotidyltransferase, EC 2.7.7.7) to initiate DNA synthesis at 13 major sites. DNA sequence analysis of the 5' termini of the newly synthesized DNA shows the predominant recognition sequences for the gene 4 protein to be 3'-C-T-G-G-G-5' or 3'-C-T-G-G-T-5'; the products of synthesis at these sites are RNA primers having the sequences pppA-C-C-C or pppA-C-C-A. The gene 4 protein can also synthesize primers at the sequences 3'-C-T-G-G-AC-5' and 3'-C-T-G-T-N-5', although these sites are used less than 10% as frequently as the predominant sites. Comparison of the utilization of primer sites suggests that the gene 4 protein binds randomly to single-stranded DNA and then translocates along the DNA in a unidirectional 5'-to-3' direction with regard to the DNA strand in search of recognition sequences. Models are presented for the role of the gene 4 protein in the initiation of lagging-strand synthesis and in the initiation of DNA replication at the origin.
机译:T7噬菌体的基因4蛋白识别单链DNA上的特定序列,然后催化与模板互补的四核糖核苷酸引物的合成。以phi X174 DNA为模板,基因4蛋白可使T7 DNA聚合酶(脱氧核苷三磷酸:DNA脱氧核苷酸转移酶,EC 2.7.7.7)在13个主要位点启动DNA合成。对新合成的DNA的5'末端的DNA序列分析表明,基因4蛋白的主要识别序列是3'-C-T-G-G-G-5'或3'-C-T-G-G-T-5'。在这些位点的合成产物是具有序列pppA-C-C-C或pppA-C-C-A的RNA引物。基因4蛋白还可以合成序列3'-C-T-G-G-AC-5'和3'-C-T-G-T-N-5'的引物,尽管这些位点的使用频率少于主要位点的10%。引物位点利用的比较表明,基因4蛋白随机结合到单链DNA,然后沿着DNA相对于DNA链以单向5'到3'方向移位,以寻找识别序列。提出了关于基因4蛋白在滞后链合成的起始和起始DNA复制中的作用的模型。

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