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编码转化相关蛋白p53的全长小鼠cDNA序列的克隆及表达分析

Cloning and expression analysis of full length mouse cDNA sequences encoding the transformation associated protein p53.

作者信息

Jenkins J R, Rudge K, Redmond S, Wade-Evans A

出版信息

Nucleic Acids Res. 1984 Jul 25;12(14):5609-26. doi: 10.1093/nar/12.14.5609.

Abstract

We have cloned and sequenced overlapping cDNA fragments which together encode the entire mouse protein p53. Using these cDNA's we have reconstructed the full length coding region for the protein, and have analysed its coding potential by expression in vitro, both as a full length sequence and as a subfragment contained in a fusion protein. The predicted amino acid sequence contains no obvious homologies to any known oncogenes but includes a possible tyrosine kinase acceptor site.

摘要

我们已经克隆并测序了重叠的cDNA片段,这些片段共同编码整个小鼠p53蛋白。利用这些cDNA,我们重建了该蛋白的全长编码区,并通过体外表达对其编码潜能进行了分析,包括全长序列以及融合蛋白中包含的一个亚片段。预测的氨基酸序列与任何已知的癌基因均无明显同源性,但包含一个可能的酪氨酸激酶受体位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d590/320018/a4d04aeeefec/nar00332-0079-a.jpg

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