Jenkins T M, Saxena J K, Kumar A, Wilson S H, Ackerman E J
Genetics and Biochemistry Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.
Science. 1992 Oct 16;258(5081):475-8. doi: 10.1126/science.1411545.
The identities of the DNA polymerases required for conversion of single-strand (ss) M13 DNA to double-strand (ds) M13 DNA were examined both in injected Xenopus laevis oocytes and in an oocyte nuclear extract. Inhibitors and antibodies specific to DNA polymerases alpha and beta were used. In nuclear extracts, inhibition by the antibody to polymerase beta could be reversed by purified polymerase beta. The polymerase beta inhibitors, dideoxythymidine triphosphate (ddTTP) and dideoxycytidine triphosphate (ddCTP), also blocked DNA synthesis and indicated that polymerase beta is involved in the conversion of ssDNA to dsDNA. These results also may have particular significance for emerging evidence of an ssDNA replication mode in eukaryotic cells.
在注射了非洲爪蟾卵母细胞和卵母细胞核提取物中,研究了将单链(ss)M13 DNA转化为双链(ds)M13 DNA所需的DNA聚合酶的特性。使用了对DNA聚合酶α和β特异的抑制剂和抗体。在核提取物中,针对聚合酶β的抗体的抑制作用可被纯化的聚合酶β逆转。聚合酶β抑制剂双脱氧胸苷三磷酸(ddTTP)和双脱氧胞苷三磷酸(ddCTP)也阻断了DNA合成,表明聚合酶β参与了ssDNA到dsDNA的转化。这些结果对于真核细胞中ssDNA复制模式的新证据可能也具有特殊意义。