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海拉细胞脱氧核糖核酸依赖性RNA聚合酶:Ⅲ类酶的功能与特性

HeLa cell deoxyribonucleic acid dependent RNA polymerases: function and properties of the class III enzymes.

作者信息

Weil P A, Blatti S P

出版信息

Biochemistry. 1976 Apr 6;15(7):1500-9. doi: 10.1021/bi00652a022.

Abstract

The class III DNA dependent RNA polymerases (nucleoside triphosphate:RNA nucleotidyltransferase EC 2.7.7.6 from HeLa cells have been solubilized and characterized as to function and properties. Two chromatographically distinct forms of enzyme III, designated polymerases IIIA and IIIB, can be resolved when cell extracts are chromatographed on DEAE-Sephadex columns. Enzymes IIIA and IIIB exhibit nearly identical catalytic properties such as divalent cation stimulation, broad biphasic ammonium sulfate optima, and characteristic alpha-amanitin sensitivities which clearly distinguish them from the homologous enzymes, forms I and II. Polymerases IIIA and IIIB are both primarily localized in the nucleus (greater than 60%). The most notable characteristic of the class III enzymes is a unique sensitivity to inhibition by alpha-amanitin (50% inhibition at 15 mug/ml). HeLa cell enzyme I is not inhibited by the mushroom toxin even at very high concentrations (greater than 400 mug/ml), while HeLa cell polymerase II is inhibited by very low concentrations of amanitin (50% inhibition at 0.003 mug/ml). The three major classes of enzyme (I, II, III) exhibit characteristic sensitivities to alpha-amanitin whether assayed in nuclei, crude homogenates, or in a chromatographically purified state. Using a nuclear in vitro RNA synthesizing system to investigate the alpha-amanitin sensitivities of the synthesis of tRNA precursor (4.5S pre-tRNA) and 5S ribosomal RNA, it was found that the synthesis of these RNA species was inhibited 50% at 15 mug/ml of alpha-amanitin. The alpha-amanitin inhibition curves for the synthesis of pre-tRNA-5S ribosomal RNA in nuclei and the alpha-amanitin titration curves for the partially purified class III enzymes (IIIA and IIIB) are identical. These data, therefore, show that the in vivo functional role of the class III RNA polymerases (IIIA-IIIB) is the transcription of the genes coding for transfer RNA and 5S ribosomal RNA.

摘要

III类DNA依赖性RNA聚合酶(来自HeLa细胞的核苷三磷酸:RNA核苷酸转移酶EC 2.7.7.6)已被溶解,并对其功能和性质进行了表征。当细胞提取物在DEAE-葡聚糖凝胶柱上进行层析时,可以分离出两种色谱上不同的酶III形式,分别称为聚合酶IIIA和IIIB。酶IIIA和IIIB表现出几乎相同的催化特性,如二价阳离子刺激、宽双相硫酸铵最适浓度以及特征性的α-鹅膏蕈碱敏感性,这使它们与同源酶I和II明显区分开来。聚合酶IIIA和IIIB主要都定位于细胞核(大于60%)。III类酶最显著的特征是对α-鹅膏蕈碱抑制具有独特的敏感性(在15微克/毫升时50%抑制)。HeLa细胞酶I即使在非常高的浓度(大于400微克/毫升)下也不会被这种蘑菇毒素抑制,而HeLa细胞聚合酶II则被非常低浓度的鹅膏蕈碱抑制(在0.003微克/毫升时50%抑制)。这三类主要的酶(I、II、III),无论在细胞核、粗匀浆中还是在色谱纯化状态下进行检测,都表现出对α-鹅膏蕈碱的特征性敏感性。使用细胞核体外RNA合成系统来研究tRNA前体(4.5S前体tRNA)和5S核糖体RNA合成的α-鹅膏蕈碱敏感性,发现这些RNA种类的合成在15微克/毫升的α-鹅膏蕈碱时被抑制50%。细胞核中前体tRNA - 5S核糖体RNA合成的α-鹅膏蕈碱抑制曲线与部分纯化的III类酶(IIIA和IIIB)的α-鹅膏蕈碱滴定曲线相同。因此,这些数据表明III类RNA聚合酶(IIIA - IIIB)在体内的功能作用是转录编码转移RNA和5S核糖体RNA的基因。

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