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噬菌体T7基因4蛋白合成RNA引物的模板识别序列。

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

作者信息

Tabor S, Richardson C C

出版信息

Proc Natl Acad Sci U S A. 1981 Jan;78(1):205-9. doi: 10.1073/pnas.78.1.205.

Abstract

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.

摘要

噬菌体T7的基因4蛋白可识别单链DNA上的特定序列,然后催化合成与模板互补的四核糖核苷酸引物。以φX174 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个主要位点起始DNA合成。对新合成DNA 5'末端的DNA序列分析表明,基因4蛋白的主要识别序列为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蛋白也可在3'-C-T-G-G-AC-5'和3'-C-T-G-T-N-5'序列处合成引物,尽管这些位点的使用频率不到主要位点的10%。对引物位点利用情况的比较表明,基因4蛋白随机结合到单链DNA上,然后沿着DNA以相对于DNA链从5'到3'的单向方向移位,以寻找识别序列。文中提出了基因4蛋白在滞后链合成起始及在复制起点处DNA复制起始中作用的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb05/319020/ab668dc6f4c1/pnas00652-0229-a.jpg

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