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在567肝癌细胞系和原代肝细胞培养物的细胞周期G1期早期,复制因子C的A1p145亚基的核募集情况。

Nuclear recruitment of A1p145 subunit of replication factor C in the early G1 phase of the cell cycle in Faza 567 hepatoma cell line and hepatocyte primary cultures.

作者信息

Levavasseur F, Burbelo P D, Cariou S, Liétard J, Yamada Y, Clément B

机构信息

Unité de Recherches Hépatologiques U 49 de l'INSERM, CHRU Pontchaillou, Rennes, France.

出版信息

FEBS Lett. 1995 Apr 17;363(1-2):132-6. doi: 10.1016/0014-5793(95)00305-s.

Abstract

Using a combination of immunoprecipitation and Western blotting with Faza 567 hepatoma cell extracts revealed that the large subunit of replication factor C (A1p145; mRFC140) was in a complex with proliferating cell nuclear antigen (PCNA). Western blotting showed that A1p145 was more abundant in nuclear extracts from butyrate-treated hepatoma cells which blocks the cells in the G1 phase of the cell cycle than from routinely cultured cells. Indirect immunoperoxidase analysis of G1 blocked Faza hepatoma cells localized A1p145 protein predominantly in the nucleoli. When hepatoma cells were stimulated to progress toward the S phase, A1p145 protein was then observed in both the cytoplasm and the nucleoplasm of these cells. Studies with early cultured normal hepatocytes which are progressing from G0 towards G1, also showed a nucleolus distribution for A1p145. This is the first demonstration in mammalian cells that the large subunit of replication factor C is associated with PCNA in the nucleus and that its distribution within cells changes during the cell cycle.

摘要

利用免疫沉淀和蛋白质印迹法相结合,对Faza 567肝癌细胞提取物进行分析,结果显示复制因子C的大亚基(A1p145;mRFC140)与增殖细胞核抗原(PCNA)形成复合物。蛋白质印迹法表明,与常规培养的细胞相比,在丁酸盐处理的肝癌细胞(其将细胞阻滞在细胞周期的G1期)的核提取物中,A1p145更为丰富。对处于G1期阻滞的Faza肝癌细胞进行间接免疫过氧化物酶分析,结果显示A1p145蛋白主要定位于核仁。当肝癌细胞被刺激进入S期时,在这些细胞的细胞质和核质中均观察到A1p145蛋白。对从G0期向G1期进展的早期培养正常肝细胞的研究也表明,A1p145呈核仁分布。这是在哺乳动物细胞中首次证明复制因子C的大亚基在细胞核中与PCNA相关,并且其在细胞内的分布在细胞周期中会发生变化。

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