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利用未受精海胆卵的内质网 - DNA - 聚合酶复合物进行体外DNA合成。

DNA synthesis in vitro with an endoplasmic-reticulum-DNA-polymerase complex from unfertilized sea urchin eggs.

作者信息

Shioda M

出版信息

Eur J Biochem. 1986 Nov 3;160(3):571-8. doi: 10.1111/j.1432-1033.1986.tb10076.x.

Abstract

An endoplasmic-reticulum-DNA-polymerase complex was prepared from unfertilized sea urchin eggs and its DNA-synthesizing activity was examined using single-stranded DNA of bacteriophage fd as a template. The complex catalyzed the ribonucleotide-dependent DNA synthesis which required dNTPs, NTPs, Mg2+ and single-stranded DNA. The DNA synthesis was sensitive to aphidicolin and N-ethylmaleimide but was resistant to 2',3'-dideoxyribosylthymine 5'-triphosphate (ddTTP) and alpha-amanitin, suggesting the involvement of DNA polymerase alpha. In parallel with the DNA synthesis, a small amount of RNA was synthesized in the presence of 100 micrograms/ml alpha-amanitin. The Km value of ribonucleotides for the RNA synthesis coincided with that for the DNA synthesis, suggesting a correlation between the DNA and RNA syntheses. Labelling of the products with [gamma-32P]ATP followed by DNA digestion with pancreatic DNase I revealed the attachment of an oligoribonucleotide (7-11 bases in length) at the 5' ends of the DNA products. These observations suggest that in DNA synthesis, primer RNA synthesis occurs first, followed by DNA chain elongation. During 1-90-min incubation, the amount of the DNA synthesized increased but the length was not significantly increased. Over 80% of the number of synthesized DNA molecules comprised a single population of short DNA fragments (60-200 bases, on average 120 bases in length) and the number of fragments increased, depending on the incubation time. However, DNA fragments of various sizes (about 100-6000 bases) were synthesized with DNA polymerase alpha solubilized from the endoplasmic-reticulum-DNA-polymerase complex. All this evidence suggests that in vitro, the complex preferentially synthesizes a particular size of short DNA fragments. The significance of the fragments is discussed.

摘要

从未受精的海胆卵中制备了一种内质网 - DNA聚合酶复合物,并以噬菌体fd的单链DNA为模板检测了其DNA合成活性。该复合物催化了依赖核糖核苷酸的DNA合成,这需要脱氧核苷三磷酸(dNTPs)、核苷三磷酸(NTPs)、Mg2+和单链DNA。DNA合成对阿非迪霉素和N - 乙基马来酰胺敏感,但对2',3'-二脱氧核糖基胸腺嘧啶5'-三磷酸(ddTTP)和α - 鹅膏蕈碱有抗性,提示有DNA聚合酶α参与。与DNA合成同时,在存在100微克/毫升α - 鹅膏蕈碱的情况下合成了少量RNA。RNA合成中核糖核苷酸的Km值与DNA合成中的Km值一致,提示DNA和RNA合成之间存在相关性。用[γ - 32P]ATP对产物进行标记,随后用胰DNA酶I消化DNA,结果显示在DNA产物的5'端连接了一个寡核糖核苷酸(长度为7 - 11个碱基)。这些观察结果提示,在DNA合成中,首先发生引物RNA合成,随后是DNA链延伸。在1 - 90分钟的孵育过程中,合成的DNA量增加,但长度没有显著增加。超过80%的合成DNA分子数量由单一群体的短DNA片段组成(平均长度为120个碱基,长度在60 - 200个碱基之间),并且片段数量根据孵育时间而增加。然而,用从内质网 - DNA聚合酶复合物中溶解的DNA聚合酶α合成了各种大小(约100 - 6000个碱基)的DNA片段。所有这些证据表明,在体外,该复合物优先合成特定大小的短DNA片段。讨论了这些片段的意义。

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