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猴病毒40和多瘤病毒的大T抗原能有效地建立原代成纤维细胞。

Large T antigens of simian virus 40 and polyomavirus efficiently establish primary fibroblasts.

作者信息

Jat P S, Sharp P A

出版信息

J Virol. 1986 Sep;59(3):746-50. doi: 10.1128/JVI.59.3.746-750.1986.

Abstract

Recombinant retroviruses that transduce the simian virus 40 (SV40) large T antigen or the polyomavirus large T antigen as well as encoding resistance to antibiotic G418 were used to investigate whether these genes alone were sufficient for immortalization of primary cells. The results provided definitive evidence that either viral gene can efficiently establish primary fibroblasts. The capability of the SV40 large T antigen to establish primary fibroblasts was undiminished by a mutation that alters its binding to sequences within the origin of replication. Surprisingly, most of the primary cells established by the expression of the SV40 large T antigen did not have a transformed phenotype. This suggests that transformation by SV40 is not simply due to a high level of expression of the SV40 large T antigen and stabilization of cellular p53.

摘要

转导猿猴病毒40(SV40)大T抗原或多瘤病毒大T抗原并编码对抗生素G418抗性的重组逆转录病毒被用于研究这些基因单独是否足以使原代细胞永生化。结果提供了确凿证据,表明任一病毒基因都能有效地建立原代成纤维细胞。改变其与复制起点内序列结合的突变并未削弱SV40大T抗原建立原代成纤维细胞的能力。令人惊讶的是,通过SV40大T抗原表达建立的大多数原代细胞没有转化表型。这表明SV40介导的转化并非仅仅归因于SV40大T抗原的高水平表达和细胞p53的稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ecc/253254/17e5fe784036/jvirol00108-0224-a.jpg

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