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细胞剪接和转录调节蛋白p32抑制腺病毒主要晚期转录并导致RNA聚合酶II的过度磷酸化。

Cellular splicing and transcription regulatory protein p32 represses adenovirus major late transcription and causes hyperphosphorylation of RNA polymerase II.

作者信息

Ohrmalm Christina, Akusjärvi Göran

机构信息

Department of Medical Biochemistry and Microbiology, Uppsala Biomedical Center, Husargatan 3, S-751 23 Uppsala, Sweden.

出版信息

J Virol. 2006 May;80(10):5010-20. doi: 10.1128/JVI.80.10.5010-5020.2006.

Abstract

The cellular protein p32 is a multifunctional protein, which has been shown to interact with a large number of cellular and viral proteins and to regulate several important activities like transcription and RNA splicing. We have previously shown that p32 regulates RNA splicing by binding and inhibiting the essential SR protein ASF/SF2. To determine whether p32 also functions as a regulator of splicing in virus-infected cells, we constructed a recombinant adenovirus expressing p32 under the transcriptional control of an inducible promoter. Much to our surprise the results showed that p32 overexpression effectively blocked mRNA and protein expression from the adenovirus major late transcription unit (MLTU). Interestingly, the p32-mediated inhibition of MLTU transcription was accompanied by an approximately 4.5-fold increase in Ser 5 phosphorylation and an approximately 2-fold increase in Ser 2 phosphorylation of the carboxy-terminal domain (CTD). Further, in p32-overexpressing cells the efficiency of RNA polymerase elongation was reduced approximately twofold, resulting in a decrease in the number of polymerase molecules that reached the end of the major late L1 transcription unit. We further show that p32 stimulates CTD phosphorylation in vitro. The inhibitory effect of p32 on MLTU transcription appears to require the CAAT box element in the major late promoter, suggesting that p32 may become tethered to the MLTU via an interaction with the CAAT box binding transcription factor.

摘要

细胞蛋白p32是一种多功能蛋白,已被证明可与大量细胞和病毒蛋白相互作用,并调节转录和RNA剪接等多种重要活动。我们之前已经表明,p32通过结合并抑制必需的SR蛋白ASF/SF2来调节RNA剪接。为了确定p32在病毒感染细胞中是否也作为剪接调节因子发挥作用,我们构建了一种重组腺病毒,该腺病毒在可诱导启动子的转录控制下表达p32。令我们惊讶的是,结果表明p32的过表达有效地阻断了腺病毒主要晚期转录单位(MLTU)的mRNA和蛋白质表达。有趣的是,p32介导的对MLTU转录的抑制伴随着羧基末端结构域(CTD)的丝氨酸5磷酸化增加约4.5倍和丝氨酸2磷酸化增加约2倍。此外,在过表达p32的细胞中,RNA聚合酶延伸效率降低了约两倍,导致到达主要晚期L1转录单位末端的聚合酶分子数量减少。我们进一步表明,p32在体外刺激CTD磷酸化。p32对MLTU转录的抑制作用似乎需要主要晚期启动子中的CAAT盒元件,这表明p32可能通过与CAAT盒结合转录因子的相互作用与MLTU相连。

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本文引用的文献

1
Preparation of soluble extracts from adenovirus-infected cells for studies of RNA splicing.
Methods Mol Med. 2007;131:33-46. doi: 10.1007/978-1-59745-277-9_3.
2
Binary AdEasy vector systems designed for Tet-ON or Tet-OFF regulated control of transgene expression.
Virus Res. 2006 Jan;115(1):16-23. doi: 10.1016/j.virusres.2005.07.001. Epub 2005 Aug 15.
4
Identification and characterization of the promoter for the gene encoding human tripeptidyl-peptidase II.
Gene. 2005 Jan 31;345(2):249-57. doi: 10.1016/j.gene.2004.11.042. Epub 2005 Jan 5.
5
6
BRCA1 can modulate RNA polymerase II carboxy-terminal domain phosphorylation levels.
Mol Cell Biol. 2004 Aug;24(16):6947-56. doi: 10.1128/MCB.24.16.6947-6956.2004.
9
Coordination of transcription, RNA processing, and surveillance by P-TEFb kinase on heat shock genes.
Mol Cell. 2004 Jan 16;13(1):55-65. doi: 10.1016/s1097-2765(03)00526-4.
10
Pin1 modulates the structure and function of human RNA polymerase II.
Genes Dev. 2003 Nov 15;17(22):2765-76. doi: 10.1101/gad.1135503. Epub 2003 Nov 4.

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