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多瘤病毒大T抗原通过保守区域2中的序列与“pRb相关”蛋白p130结合。

Polyomavirus large T-antigen binds the "pRb related' protein p130 through sequences in conserved region 2.

作者信息

Desjardins P, Pilon A A, Hassell J A, Mes-Masson A M

机构信息

Institute for Molecular Biology and Biotechnology, McMaster University, Hamilton, Ontario, Canada.

出版信息

Virus Res. 1997 Jan;47(1):85-90. doi: 10.1016/s0168-1702(96)01404-9.

Abstract

The transforming potential of DNA tumor viruses derives mainly from the ability of their encoded oncogene products to interact with cellular proteins. Many of these viral oncoproteins share regions of sequence similarity, designated conserved region 1 and 2, which have been implicated in complex formation with pRb, the product of the retinoblastoma tumor suppressor gene, and related p107 and p130 species. It has now been shown that the EIA protein of adenovirus is able to bind to all three pRb-related proteins through sequences in conserved region 1 and 2. We have shown previously that polyomavirus large T-antigen also interacts with pRb and p107 in vitro. The pRb and p107 binding domains reside between residues 141, 158 which include conserved region 2. In the present study, we demonstrate that polyomavirus large T-antigen also interacted with p130 in vitro through the same sequences in conserved region 2.

摘要

DNA肿瘤病毒的转化潜能主要源于其编码的癌基因产物与细胞蛋白相互作用的能力。这些病毒癌蛋白中有许多具有序列相似区域,称为保守区域1和2,它们与视网膜母细胞瘤肿瘤抑制基因的产物pRb以及相关的p107和p130蛋白形成复合物有关。现已表明,腺病毒的EIA蛋白能够通过保守区域1和2中的序列与所有三种pRb相关蛋白结合。我们之前已经表明,多瘤病毒大T抗原在体外也与pRb和p107相互作用。pRb和p107结合域位于第141至158位氨基酸残基之间,其中包括保守区域2。在本研究中,我们证明多瘤病毒大T抗原在体外也通过保守区域2中的相同序列与p130相互作用。

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