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一种具有致癌潜力的新型假定酪氨酸激酶受体。

A novel putative tyrosine kinase receptor with oncogenic potential.

作者信息

Janssen J W, Schulz A S, Steenvoorden A C, Schmidberger M, Strehl S, Ambros P F, Bartram C R

机构信息

Department of Pediatrics II, University of Ulm, Germany.

出版信息

Oncogene. 1991 Nov;6(11):2113-20.

PMID:1834974
Abstract

We have detected transforming activity by a tumorigenicity assay using NIH3T3 cells transfected with DNA from a chronic myeloproliferative disorder patient. Here, we report the cDNA cloning of the corresponding oncogene, designated UFO, in allusion to the as yet unidentified function of its protein. Nucleotide sequence analysis of a 3116bp cDNA clone revealed a 2682-bp-long open reading frame capable of directing the synthesis of a 894 amino acid polypeptide. The predicted UFO protein exhibits characteristic features of a transmembrane receptor with associated tyrosine kinase activity. The UFO proto-oncogene maps to human chromosome 19q13.1 and is transcribed into two 5.0 kb and 3.2 kb mRNAs in human bone marrow and human tumor cell lines. The UFO locus is evolutionarily conserved between vertebrate species. A 4.0 kb mRNA of the murine UFO homolog is expressed in a variety of different mouse tissues. We thus have identified a novel element of the complex signaling network involved in the control of cell proliferation and differentiation.

摘要

我们通过致瘤性分析检测到了转化活性,该分析使用了用慢性骨髓增殖性疾病患者的DNA转染的NIH3T3细胞。在此,我们报告了相应致癌基因的cDNA克隆,因其蛋白质功能尚未明确,故命名为UFO。对一个3116bp cDNA克隆的核苷酸序列分析揭示了一个2682bp长的开放阅读框,能够指导合成一个894个氨基酸的多肽。预测的UFO蛋白具有跨膜受体的特征,并具有相关的酪氨酸激酶活性。UFO原癌基因定位于人类染色体19q13.1,在人类骨髓和人类肿瘤细胞系中转录为两种5.0kb和3.2kb的mRNA。UFO基因座在脊椎动物物种之间具有进化保守性。小鼠UFO同源物的一个4.0kb mRNA在多种不同的小鼠组织中表达。因此,我们鉴定出了参与细胞增殖和分化控制的复杂信号网络中的一个新元件。

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