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来自正常和多瘤病毒转化的BHK-21/C13细胞的脱氧核糖核酸依赖性核糖核酸聚合酶

Deoxyribonucleic acid-dependent ribonucleic acid polymerases from normal and polyoma-transformed BHK-21/C13 cells.

作者信息

Cooper R J, Keir H M

出版信息

Biochem J. 1975 Mar;145(3):509-16. doi: 10.1042/bj1450509.

Abstract

DNA-dependent RNA polymerase (EC 2.7.7.6) ACTIVITIES FROM NORMAL BHK-21/C13 cells and from BHK-21/C13 cells transformed by polyoma virus (PYY cells) were solubilized and fractionated on columns of DEAE-Sephadex. Various properties of the A and B enzymes from the two types of cell were compared. 1. The yields of polymerase relative to the DNA content of the nuclear preparations are similar for both cell types. 2. The ionic-strength optima of polymerases A and B are 12.5 mM and 100mM with respect to (NH4)2SO4 for both cell types. 3. The Mn2+/Mg2+ activity ratio (measured at the respective optimum for each cation) for polymerase A from BHK-21/C13 cells was 1.48 and for the polymerase A from PYY cells was 0.55. The corresponding ratios for polymerase B were 10.11 for BHK-21/C13 cells and 22.75 for PYY cells. 4. Minor differences in the ability of the A polymerases to transcribe native and denatured DNA templates were observed; such differences were not apparent when the B polymerases were compared. 5. All the polymerases were inhibited completely by actinomycin D and by rifampicin AF/013, but not markedly so by rifampicin. Alpha-amanitin inhibited polymerase B but not polymerase A.

摘要

从正常的BHK - 21/C13细胞以及被多瘤病毒转化的BHK - 21/C13细胞(PYY细胞)中提取依赖DNA的RNA聚合酶(EC 2.7.7.6)活性,并使其溶解,然后在二乙氨基乙基葡聚糖(DEAE - Sephadex)柱上进行分级分离。比较了这两种细胞中A和B两种酶的各种特性。1. 相对于核制剂的DNA含量,两种细胞类型的聚合酶产量相似。2. 两种细胞类型中,聚合酶A和B的离子强度最佳值(相对于硫酸铵)分别为12.5 mM和100 mM。3. BHK - 21/C13细胞的聚合酶A的Mn2+/Mg2+活性比(在每种阳离子各自的最佳条件下测量)为1.48,PYY细胞的聚合酶A的该比值为0.55。BHK - 21/C13细胞的聚合酶B的相应比值为10.11,PYY细胞的为22.75。4. 观察到A聚合酶转录天然和变性DNA模板的能力存在细微差异;比较B聚合酶时,这种差异不明显。5. 所有聚合酶都被放线菌素D和利福平AF/013完全抑制,但未被利福平显著抑制。α - 鹅膏蕈碱抑制聚合酶B,但不抑制聚合酶A。

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本文引用的文献

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Ribosomal RNA synthesis and RNA polymerase.核糖体RNA合成与RNA聚合酶。
Nature. 1970 Dec 5;228(5275):993-5. doi: 10.1038/228993a0.

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