首页> 美国卫生研究院文献>Nucleic Acids Research >Primer RNA for DNA synthesis on single-stranded DNA template in a cell free system from Drosophila melanogaster embryos.
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Primer RNA for DNA synthesis on single-stranded DNA template in a cell free system from Drosophila melanogaster embryos.

机译:用于从果蝇胚胎无细胞系统中的单链DNA模板上进行DNA合成的引物RNA。

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摘要

A cytoplasmic extract of Drosophila melanogaster early embryos supported DNA synthesis which was dependent on an added single stranded DNA template, phi X174 viral DNA. The product DNA made during early reaction was about 100 to 600 nucleotides in length and complementary to the added template. After alkali treatment, 70 to 80 per cent of the product DNA chains exposed 5'-hydroxyl ends, suggesting covalent linkage of primer RNA at their 5'-ends. Post-labeling of 5'-ends of the product DNA with polynucleotide kinase and [gamma-32P]ATP revealed that oligoribonucleotides, mainly hexa- and heptanucleotides, were covalently linked to the 5'-ends of the majority of the DNA chains. The nucleotide sequence of the linked RNA was mainly 5'(p)ppApA(prN)4-5, where tri- (or di-) phosphate terminus was detected by the acceptor activity for the cap structure with guanylyltransferase and [alpha-32P]GTP. The structure of this primer RNA was comparable to that of the octaribonucleotide primer isolated from the nuclei of Drosophila early embryos.
机译:果蝇早期胚胎的细胞质提取物支持DNA合成,DNA合成依赖于添加的单链DNA模板phi X174病毒DNA。在早期反应过程中产生的产物DNA长度约为100至600个核苷酸,并与所添加的模板互补。碱处理后,70%至80%的产品DNA链暴露5'-羟基末端,表明引物RNA在其5'-末端共价连接。用多核苷酸激酶和[γ-32P] ATP对产物DNA的5'末端进行后标记显示,寡核糖核苷酸(主要是六核苷酸和七核苷酸)与大多数DNA链的5'末端共价连接。连接的RNA的核苷酸序列主要是5'(p)ppApA(prN)4-5,其中通过鸟苷基转移酶和[alpha-32P]通过帽结构的受体活性检测到磷酸三(或二)磷酸末端。 GTP。该引物RNA的结构与从果蝇早期胚胎的核中分离的八核糖核苷酸引物的结构相当。

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