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HeLa细胞、人正常成纤维细胞和诺维科夫肝癌细胞的U1、U2和U3小核RNA的核糖核酸酶T1指纹图谱比较。

Comparison of RNase T1 fingerprints of U1, U2, and U3 small nuclear RNA's of HeLa cells, human normal fibroblasts, and Novikoff hepatoma cells.

作者信息

Nohga K, Reddy R, Busch H

出版信息

Cancer Res. 1981 Jun;41(6):2215-20.

PMID:6165460
Abstract

To determine whether there are differences between the U1, U2, and U3 small nuclear RNA's of human cancer cells (HeLa cells) and human normal fibroblasts (IMR-90 cells), and between these uridine-rich small nuclear RNA's of human and Novikoff hepatoma cells, the cells were first incubated in Eagle's medium with [32P]Pi to label these RNA's uniformly. No differences were found between the RNase T1 fingerprints of the purified U1, U2, and U3 RNA's of HeLa cells and IMR-90 cells. The RNase T1 fingerprints of U1 RNA's from human tissues were very similar to that of the U1 RNA of Novikoff hepatoma cells. The RNase T1 fingerprints of U2 and U3 RNA's from human tissues had many similarities to those of Novikoff hepatoma cells, but a few differences were found, such as a point mutation of the U-U-Gp in the rat U2 RNA to A-U-Gp (U leads to A) in human U2 RNA. Unlike the three U3 RNA's of Novikoff hepatoma cells, U3 RNA from human tissues appears to be only one species. These results indicate that U1, U2, and U3 RNA's of human cancer cells are essentially the same as those of human normal cells. In addition, the uridine-rich small nuclear RNA's appear to be conserved through evolution.

摘要

为了确定人类癌细胞(HeLa细胞)与人类正常成纤维细胞(IMR-90细胞)的U1、U2和U3小核RNA之间,以及人类和诺维科夫肝癌细胞的这些富含尿苷的小核RNA之间是否存在差异,首先将细胞在含有[32P]Pi的伊格尔培养基中孵育,以均匀标记这些RNA。HeLa细胞和IMR-90细胞纯化后的U1、U2和U3 RNA的核糖核酸酶T1指纹图谱未发现差异。来自人类组织的U1 RNA的核糖核酸酶T1指纹图谱与诺维科夫肝癌细胞的U1 RNA非常相似。来自人类组织的U2和U3 RNA的核糖核酸酶T1指纹图谱与诺维科夫肝癌细胞的指纹图谱有许多相似之处,但也发现了一些差异,例如大鼠U2 RNA中的U-U-Gp点突变为人类U2 RNA中的A-U-Gp(U变为A)。与诺维科夫肝癌细胞的三种U3 RNA不同,来自人类组织的U3 RNA似乎只有一种。这些结果表明,人类癌细胞的U1、U2和U3 RNA与人类正常细胞的基本相同。此外,富含尿苷的小核RNA似乎在进化过程中是保守的。

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