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通过基因打靶使小鼠N-ras基因失活。

Inactivation of the murine N-ras gene by gene targeting.

作者信息

Cases S, Dautry F

机构信息

Laboratoire d'Oncologie Moléculaire, CNRS UA 1158, Institut Gustave Roussy, Villejuif, France.

出版信息

Oncogene. 1992 Dec;7(12):2525-8.

PMID:1461656
Abstract

The mammalian ras genes have been implicated in the genesis of a wide variety of tumors. Although it is likely that they play an essential role in signal transduction, their specific function is still unknown. To initiate a genetic analysis of the ras genes in mammals we inactivated the N-ras gene in murine embryonic stem cells by gene targeting. The frequency of integration at the N-ras locus of our targeting vector being low (of the order of 1/5000 transfectants), we used a positive/negative selection followed by an analysis of individual colonies in order to minimize the in vitro manipulation of the embryonic stem cells. Using this approach, we isolated two clones of ES cells with one inactivated N-ras allele. These cells have no distinctive phenotype either in vitro or in vivo in chimeric mice.

摘要

哺乳动物的ras基因与多种肿瘤的发生有关。尽管它们可能在信号转导中起关键作用,但其具体功能仍不清楚。为了对哺乳动物的ras基因进行遗传分析,我们通过基因打靶使小鼠胚胎干细胞中的N-ras基因失活。由于我们的打靶载体在N-ras位点的整合频率较低(约为1/5000转染子),我们采用了正负筛选法,随后对单个菌落进行分析,以尽量减少对胚胎干细胞的体外操作。通过这种方法,我们分离出了两个ES细胞克隆,其中一个N-ras等位基因失活。这些细胞在体外或嵌合小鼠体内均无明显表型。

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