Suppr超能文献

猿猴病毒40 tsA突变体大T抗原在tsA N型和A型转化体中的表型特异性磷酸化。

Phenotype-specific phosphorylation of simian virus 40 tsA mutant large T antigens in tsA N-type and A-type transformants.

作者信息

Knippschild U, Kiefer J, Patschinsky T, Deppert W

机构信息

Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie, Universität Hamburg, Federal Republic of Germany.

出版信息

J Virol. 1991 Aug;65(8):4414-23. doi: 10.1128/JVI.65.8.4414-4423.1991.

Abstract

To identify molecular differences between simian virus 40 (SV40) tsA58 mutant large tumor antigen (large T) in cells of tsA58 N-type transformants [FR(tsA58)A cells], which revert to the normal phenotype after the cells are shifted to the nonpermissive growth temperature, and mutant large T in tsA58 A-type transformants [FR(tsA58)57 cells], which maintain their transformed phenotype after the temperature shift, we asked whether the biological activity of these mutant large T antigens at the nonpermissive growth temperature might correlate with phosphorylation at specific sites. At the permissive growth temperature, the phosphorylation patterns of the mutant large T proteins in FR(tsA58)A (N-type) cells and in FR(tsA58)57 (A-type) cells were largely indistinguishable from that of wild-type large T in FR(wt648) cells. After a shift to the nonpermissive growth temperature, no significant changes in the phosphorylation patterns of wild-type large T in FR(wt648) or of mutant large T in FR(tsA58)57 (A-type) cells were observed. In contrast, the phosphorylation pattern of mutant large T in FR(tsA58)A (N-type) cells changed in a characteristic manner, leading to an apparent underphosphorylation at specific sites. Phosphorylation of the cellular protein p53 was analyzed in parallel. Characteristic differences in the phosphorylation pattern of p53 were observed when cells of N-type and A-type transformants were kept at 39 degrees C as opposed to 32 degrees C. However, these differences did not relate to the different phenotypes of FR(tsA58)A (N-type) and FR(tsA58)57 (A-type) cells at the nonpermissive growth temperature. Our results, therefore, suggest that phosphorylation of large T at specific sites correlates with the transforming activity of tsA mutant large T in SV40 N-type and A-type transformants. This conclusion was substantiated by demonstrating that the biological properties as well as the phosphorylation patterns of SV40 tsA28 mutant large T in cells of SV40 tsA28 N-type and A-type transformants were similar to those in FR(tsA58)A (N-type) and in FR(tsA58)57 (A-type) cells, respectively. The phenotype-specific phosphorylation of tsA mutant large T in tsA A-type transformants probably is a cellular process induced during establishment of SV40 tsA A-type transformants, since tsA28 A-type transformant cells could be obtained by a large-T-dependent in vitro progression of cells of the tsA28 N-type transformant tsA28.3 (M. Osborn and K. Weber, J. Virol. 15:636-644, 1975).

摘要

为了鉴别猿猴病毒40(SV40)tsA58突变型大T抗原在tsA58 N型转化细胞[FR(tsA58)A细胞]中的分子差异,这些细胞在转移到非允许生长温度后会恢复到正常表型,以及tsA58 A型转化细胞[FR(tsA58)57细胞]中的突变型大T抗原的差异,这些细胞在温度转移后仍保持其转化表型,我们探究了这些突变型大T抗原在非允许生长温度下的生物学活性是否可能与特定位点的磷酸化相关。在允许生长温度下,FR(tsA58)A(N型)细胞和FR(tsA58)57(A 型)细胞中突变型大T蛋白的磷酸化模式与FR(wt648)细胞中野生型大T的磷酸化模式基本无法区分。转移到非允许生长温度后,未观察到FR(wt648)中野生型大T或FR(tsA58)57(A 型)细胞中突变型大T的磷酸化模式有显著变化。相比之下,FR(tsA58)A(N型)细胞中突变型大T的磷酸化模式以一种特征性方式发生变化,导致特定位点明显磷酸化不足。同时对细胞蛋白p53的磷酸化进行了分析。当N型和A型转化细胞在39℃而非32℃下培养时,观察到p53磷酸化模式存在特征性差异。然而,这些差异与FR(tsA58)A(N型)和FR(tsA58)57(A 型)细胞在非允许生长温度下的不同表型无关。因此,我们的结果表明,特定位点的大T磷酸化与SV40 N型和A型转化细胞中tsA突变型大T的转化活性相关。通过证明SV40 tsA28 N型和A型转化细胞中SV40 tsA28突变型大T的生物学特性以及磷酸化模式分别与FR(tsA58)A(N型)和FR(tsA58)57(A 型)细胞中的相似,这一结论得到了证实。tsA A型转化细胞中tsA突变型大T的表型特异性磷酸化可能是SV40 tsA A型转化细胞建立过程中诱导的细胞过程,因为tsA28 A型转化细胞可以通过tsA28 N型转化细胞tsA28.3的大T依赖性体外进展获得(M.奥斯本和K.韦伯,《病毒学杂志》15:636 - 644,1975)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad06/248881/795b1a08cc00/jvirol00051-0456-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验