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首页> 外文期刊>Virology >Adenovirus E4 34k and E4 11k inhibit double strand break repair and are physically associated with the cellular DNA-dependent protein kinase.
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Adenovirus E4 34k and E4 11k inhibit double strand break repair and are physically associated with the cellular DNA-dependent protein kinase.

机译:腺病毒E4 34k和E4 11k抑制双链断裂修复,并与细胞DNA依赖性蛋白激酶物理相关。

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摘要

The adenovirus oncoproteins E4 34k and E4 11k, the products of E4 open reading frames 6 and 3, respectively, individually prevent the formation of concatemers of the linear viral genome in infected cells. We show here that genome concatenation in E4 mutant-infected cells requires the cellular DNA-dependent protein kinase (DNA PK) and that E4 34k inhibits V(D)J recombination, a normal cellular process that is also dependent on DNA PK. We further show that both E4 34k and E4 11k coimmunoprecipitate with DNA PK. These observations indicate that E4 products block formation of concatemers of the viral genome by inhibiting DNA PK-dependent double strand break repair and suggest that they act by forming a physical complex with DNA PK. DNA PK also participates in activation of p53 DNA-binding activity by DNA damage. By inhibiting DNA PK function, E4 products may block p53 activation in response to the products of viral DNA replication and thus provide a new mechanism to prevent apoptosis of infected cells. Copyright 1999 Academic Press.
机译:E4开放阅读框6和3的产物腺病毒癌蛋白E4 34k和E4 11k分别阻止了线性病毒基因组连接体在感染细胞中的形成。我们在这里显示,E4突变感染的细胞中的基因组串联需要细胞DNA依赖性蛋白激酶(DNA PK),而E4 34k抑制V(D)J重组,这也是一种正常的细胞过程,也依赖于DNA PK。我们进一步表明,E4 34k和E4 11k都与DNA PK共免疫沉淀。这些观察结果表明,E4产物通过抑制DNA PK依赖性双链断裂修复来阻断病毒基因组串联体的形成,并表明它们通过与DNA PK形成物理复合物起作用。 DNA PK还通过DNA损伤参与激活p53 DNA结合活性。通过抑制DNA PK功能,E4产物可响应病毒DNA复制产物而阻断p53激活,从而提供了一种防止感染细胞凋亡的新机制。版权所有1999,学术出版社。

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