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卤虫的DNA依赖性RNA聚合酶:发育中幼虫的聚合酶活性降低及聚合酶II分子数量减少

DNA-dependent RNA polymerases from Artemia salina: decreasing polymerase activities and number of polymerase II molecules in developing larvae.

作者信息

Bagshaw J C, Bernstein R S, Bond B H

出版信息

Differentiation. 1978 Jan 13;10(1):13-21. doi: 10.1111/j.1432-0436.1978.tb00940.x.

Abstract

Embryos and larvae of the brine shrimp, Artemia salina, provide a useful biological system for biochemical studies of animal development. Dormant encysted embryos can be cultured readily in the laboratory to provide large quantities of free-swimming nauplius larvae. The rate of synthesis of all classes of RNA in swimming larvae declines markedly between 24 and 72 h after immersion of dormant embryos in sea water. Nuclei were isolated from 24-72 h larvae and RNA polymerase activity was measured under conditions in which the nuclei remained intact. Total RNA polymerase activity of isolated nuclei decreased in parallel with RNA synthesis in vivo. RNA polymerases were solubilized from nuclei and fractionated by chromatography on DEAE-cellulose. The levels of both RNA polymerases I and II also decreased in parallel with RNA synthesis in vivo. The specific activity of highly purified RNA polymerase II was determined by comparison of enzyme activity with the mass of RNA polymerase II subunits displayed on SDS gels. The specific activities of RNA polymerase II preparations from 24 and 72 h larvae were identical. The number of polymerase II molecules was estimated from the mass of the subunits. The number of molecules per nucleus declined from 20,000 at 24 h to 3500 at 72 h.

摘要

卤虫(Artemia salina)的胚胎和幼虫为动物发育的生化研究提供了一个有用的生物系统。休眠的包囊胚胎可以在实验室中轻松培养,以提供大量自由游动的无节幼虫。将休眠胚胎浸入海水中24至72小时后,游动幼虫中各类RNA的合成速率显著下降。从24至72小时的幼虫中分离出细胞核,并在细胞核保持完整的条件下测量RNA聚合酶活性。分离细胞核的总RNA聚合酶活性与体内RNA合成平行下降。RNA聚合酶从细胞核中溶解出来,并通过DEAE-纤维素柱层析进行分级分离。RNA聚合酶I和II的水平也与体内RNA合成平行下降。通过将酶活性与SDS凝胶上显示的RNA聚合酶II亚基质量进行比较,测定了高度纯化的RNA聚合酶II的比活性。来自24小时和72小时幼虫的RNA聚合酶II制剂的比活性相同。从亚基质量估计聚合酶II分子的数量。每个细胞核中的分子数量从24小时时的20,000个下降到72小时时的3500个。

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