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编码一种假定蛋白激酶的人类癌基因的结构与转化潜能

Structure and transforming potential of the human cot oncogene encoding a putative protein kinase.

作者信息

Miyoshi J, Higashi T, Mukai H, Ohuchi T, Kakunaga T

机构信息

Department of Oncogene Research, Osaka University, Japan.

出版信息

Mol Cell Biol. 1991 Aug;11(8):4088-96. doi: 10.1128/mcb.11.8.4088-4096.1991.

Abstract

A new transforming gene has been molecularly cloned from hamster SHOK cells transformed with DNA extracted from a human thyroid carcinoma cell line and named the cot (cancer Osaka thyroid) oncogene. cDNA sequencing disclosed that this oncogene codes for a protein with 415 amino acid residues, and computer matching showed 42 to 48% similarity matches with serine protein kinases. Its gene product was identified as a 52-kDa protein by transcription and translation in vitro. Expression of cot cDNA under transcriptional control by a retroviral long terminal repeat induced morphological transformation of NIH 3T3 cells as well as SHOK cells. Protein kinase activity associated with constructed p60gag-cot was detected by immune complex kinase assay with anti-gag antiserum. The cot oncogene was overexpressed in transformed SHOK cells and found to have a rearranged 3' end in the last coding exon, which probably resulted in a deletion and an altered C' terminus in the transforming protein. This DNA rearrangement appeared to have occurred during transfection of the tumor DNA into hamster SHOK cells and not in the original thyroid tumor.

摘要

从用人类甲状腺癌细胞系提取的DNA转化的仓鼠SHOK细胞中分子克隆出一种新的转化基因,并将其命名为cot(大阪甲状腺癌)癌基因。cDNA测序表明,该癌基因编码一种含有415个氨基酸残基的蛋白质,计算机匹配显示与丝氨酸蛋白激酶有42%至48%的相似性匹配。通过体外转录和翻译,其基因产物被鉴定为一种52 kDa的蛋白质。在逆转录病毒长末端重复序列的转录控制下,cot cDNA的表达诱导了NIH 3T3细胞以及SHOK细胞的形态转化。用抗gag抗血清通过免疫复合物激酶测定法检测了与构建的p60gag-cot相关的蛋白激酶活性。cot癌基因在转化的SHOK细胞中过表达,并且发现在最后一个编码外显子中有一个重排的3'末端,这可能导致转化蛋白中出现缺失和改变的C'末端。这种DNA重排似乎发生在将肿瘤DNA转染到仓鼠SHOK细胞的过程中,而不是在原始甲状腺肿瘤中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c327/361219/a575fb1da17d/molcellb00032-0277-a.jpg

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