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Synthesis and maturation of ribosomal ribonucleic acids in isolated HeLa cell nuclei. A tracer study on the topology of the 45S precursor of ribosomal ribonucleic acids

机译:分离的HeLa细胞核中核糖体核糖核酸的合成和成熟。核糖体核糖核酸45S前体拓扑的示踪研究

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摘要

The synthesis and processing of RNA by isolated HeLa cell nuclei was studied at low ionic strength in the presence of α-amanitin. The RNA polymerase reaction, with endogenous template and enzyme, rapidly reaches a plateau dependent on the amount of nuclei. Evidence is presented that incorporation of [3H]UMP proceeds only in growing RNA chains, whereas initiation of new RNA chains is arrested. The product formed contains all the main components of the 45S pre-rRNA (precursor of rRNA) maturation pathway (45S, 32S and 20S pre-rRNA; 28S and 18S rRNA). Most of the labelled material is in the mature rRNA components and their immediate precursors, even at very short times of incubation (2min). Small, but definite, 5S and 4S RNA peaks are also observed. At shorter incubation times a substantial amount of [3H]UMP is incorporated into RNA molecules in the 24S and 10–16S zones. This RNA material is considered to represent the non-conserved segments of 45S pre-rRNA in the process of nucleolytic degradation. A model for the tracer study of the topology of 45S pre-rRNA, on arrest of rRNA initiation, is discussed. The experimental evidence obtained supports the following structure of 45S pre-rRNA: 5′-end–28S rRNA unit–18S rRNA unit–nonconserved segment–3′-end.
机译:在存在α-amanitin的情况下,以低离子强度研究了分离的HeLa细胞核对RNA的合成和加工。带有内源模板和酶的RNA聚合酶反应迅速达到稳定水平,具体取决于细胞核的数量。有证据表明,[3H] UMP的掺入仅在生长的RNA链中进行,而新RNA链的起始被阻止。形成的产物包含45S pre-rRNA(rRNA的前体)成熟途径的所有主要成分(45S,32S和20S pre-rRNA; 28S和18S rRNA)。即使在很短的孵育时间(2分钟)中,大多数标记的材料都位于成熟的rRNA成分及其直接前体中。还观察到了很小但确定的5S和4S RNA峰。在较短的孵育时间中,大量的[3H] UMP被掺入24S和10-16S区的RNA分子中。这种RNA物质被认为代表了核酸降解过程中45S pre-rRNA的非保守片段。讨论了一种用于追踪45S pre-rRNA拓扑的示踪剂研究模型,该模型可阻止rRNA起始。获得的实验证据支持45S pre-rRNA的以下结构:5'-末端–28S rRNA单位–18S rRNA单位-非保守区段–3'-末端。

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