Yoda K, Okazaki T
Nucleic Acids Res. 1983 Jun 11;11(11):3433-50. doi: 10.1093/nar/11.11.3433.
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.
果蝇早期胚胎的细胞质提取物支持DNA合成,该合成依赖于添加的单链DNA模板——φX174病毒DNA。早期反应中产生的产物DNA长度约为100至600个核苷酸,且与添加的模板互补。碱处理后,70%至80%的产物DNA链暴露5'-羟基末端,表明引物RNA在其5'-末端存在共价连接。用多核苷酸激酶和[γ-32P]ATP对产物DNA的5'-末端进行标记后发现,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的核苷酸序列主要为5'(p)ppApA(prN)4-5,其中通过鸟苷酸转移酶和[α-32P]GTP对帽结构的接受活性检测到三(或二)磷酸末端。这种引物RNA的结构与从果蝇早期胚胎细胞核中分离出的八核糖核苷酸引物的结构相当。