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腺病毒E1A蛋白抑制p53介导的转录激活。

Adenovirus E1A proteins inhibit activation of transcription by p53.

作者信息

Steegenga W T, van Laar T, Riteco N, Mandarino A, Shvarts A, van der Eb A J, Jochemsen A G

机构信息

Laboratory of Molecular Carcinogenesis, Sylvius Laboratories, Leiden University, The Netherlands.

出版信息

Mol Cell Biol. 1996 May;16(5):2101-9. doi: 10.1128/MCB.16.5.2101.

Abstract

p53 stimulates the transcription of a number of genes, such as MDM2, Waf1, and GADD45. We and others have shown previously that this activity of p53 can be inhibited by adenovirus type 2 or 12 large E1B proteins. Here we show that the adenovirus E1A proteins also can repress the stimulation of transcription by p53, both in transient transfections and in stably transfected cell lines. The inhibition by E1A occurs without a significant effect on the DNA-binding capacity of p53. Furthermore, the activity of a fusion protein containing the N-terminal part of p53 linked to the GAL4 DNA-binding domain can be suppressed by E1A. This indicates that E1A affects the transcription activation domain of p53, although tryptic phosphopeptide mapping revealed that the level of phosphorylation of this domain does not change significantly in E1A-expressing cell lines. Gel filtration studies, however, showed p53 to be present in complexes of increased molecular weight as a result of E1A expression. Apparently, E1A can cause increased homo- or hetero-oligomerization of p53, which might result in the inactivation of the transcription activation domain of p53. Additionally, we found that transfectants stably expressing E1A have lost the ability to arrest in G1 after DNA damage, indicating that E1A can abolish the normal biological function of p53.

摘要

p53可刺激多种基因的转录,如MDM2、Waf1和GADD45。我们及其他人之前已表明,p53的这种活性可被2型或12型腺病毒的大E1B蛋白抑制。在此我们表明,腺病毒E1A蛋白在瞬时转染和稳定转染的细胞系中也能抑制p53对转录的刺激作用。E1A的抑制作用对p53的DNA结合能力无显著影响。此外,包含与GAL4 DNA结合结构域相连的p53 N端部分的融合蛋白的活性也可被E1A抑制。这表明E1A影响p53的转录激活结构域,尽管胰蛋白酶磷酸肽图谱分析显示,在表达E1A的细胞系中该结构域的磷酸化水平没有显著变化。然而,凝胶过滤研究表明,由于E1A的表达,p53以分子量增加的复合物形式存在。显然,E1A可导致p53的同源或异源寡聚化增加,这可能导致p53转录激活结构域失活。此外,我们发现稳定表达E1A的转染子在DNA损伤后失去了在G1期停滞的能力,这表明E1A可消除p53的正常生物学功能。

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