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多瘤病毒中T抗原的N端氨基酸序列对蛋白激酶活性和细胞转化很重要。

N-terminal amino acid sequences of the polyoma middle-size T antigen are important for protein kinase activity and cell transformation.

作者信息

Templeton D, Eckhart W

出版信息

Mol Cell Biol. 1984 May;4(5):817-21. doi: 10.1128/mcb.4.5.817-821.1984.

Abstract

We constructed deletion mutations which removed N-terminal coding sequences of various lengths from a cloned polyoma middle-size T antigen (MT antigen) gene. We introduced the MT antigen genes into a simian virus 40 expression vector so that they were expressed at high levels under the control of the simian virus 40 late promoter in COS-1 cells. The deletion mutant genes synthesized truncated MT antigens whose size was consistent with the deletion of either 70 or 106 amino acids from N termini, owing to initiation of translation at internal methionine codons in the MT antigen-coding region. The truncated MT antigens were found in cell membrane fractions but failed to show MT antigen-associated protein kinase activity. The cloned deletion mutant DNAs failed to transform rat F2408 or mouse NIH 3T3 cells. Therefore, N-terminal amino acid sequences of the polyoma MT antigen, as well as C-terminal sequences, are important for protein kinase activity and cell transformation.

摘要

我们构建了缺失突变体,从克隆的多瘤病毒中号T抗原(MT抗原)基因去除了不同长度的N端编码序列。我们将MT抗原基因导入猿猴病毒40表达载体,使其在COS-1细胞中猿猴病毒40晚期启动子的控制下高水平表达。由于在MT抗原编码区内部甲硫氨酸密码子处起始翻译,缺失突变体基因合成了截短的MT抗原,其大小与从N端缺失70或106个氨基酸一致。截短的MT抗原存在于细胞膜组分中,但未显示出与MT抗原相关的蛋白激酶活性。克隆的缺失突变体DNA未能转化大鼠F2408或小鼠NIH 3T3细胞。因此,多瘤病毒MT抗原的N端氨基酸序列以及C端序列对于蛋白激酶活性和细胞转化都很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf8/368818/d1359ada002f/molcellb00147-0009-a.jpg

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