Siegel R L, Kalf G F
J Biol Chem. 1982 Feb 25;257(4):1785-90.
DNA synthesis in vitro was studied in rat giant trophoblast nuclei from parietal yolk sacs at Day 13 of development. These nuclei synthesize DNA by a series of endoreduplications in the absence of mitosis. Although the nuclei contain DNA polymerase alpha and beta activities, polymerase alpha activity is not expressed since DNA synthesis is insensitive to aphidicolin. In contrast, N-ethylmaleimide and the DNA polymerase beta inhibitors, 50 mM potassium phosphate, and 2',3'-dideoxythymidine triphosphate inhibit DNA synthesis in isolated nuclei to a degree identical with that seen with partially purified trophoblast DNA polymerase beta, suggesting that polymerase beta is the major polymerase activity in Day 13 trophoblast nuclei. DNA synthesis by these nuclei is dependent on ATP and inhibited by novobiocin and has been shown to be replicative rather than repair-type synthesis, since the newly synthesized DNA is contiguous with DNA replicated in vivo in the presence of a bromodeoxyuridine density label. The results suggest that DNA endoreduplication in these nuclei is being carried out by DNA polymerase beta.
在发育第13天,对来自壁内卵黄囊的大鼠巨大滋养层细胞核的体外DNA合成进行了研究。这些细胞核在无有丝分裂的情况下通过一系列核内复制来合成DNA。尽管细胞核含有DNA聚合酶α和β活性,但由于DNA合成对阿非迪霉素不敏感,聚合酶α活性未表达。相反,N-乙基马来酰亚胺以及DNA聚合酶β抑制剂50 mM磷酸钾和2',3'-双脱氧胸苷三磷酸对分离细胞核中的DNA合成的抑制程度与部分纯化的滋养层DNA聚合酶β相同,这表明聚合酶β是第13天滋养层细胞核中的主要聚合酶活性。这些细胞核的DNA合成依赖于ATP,并受到新生霉素的抑制,且已被证明是复制性而非修复型合成,因为新合成的DNA与在存在溴脱氧尿苷密度标记的情况下体内复制的DNA是连续的。结果表明,这些细胞核中的DNA核内复制是由DNA聚合酶β进行的。