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Poliovirus-induced inhibition of host RNA synthesis studied in isolated HEp-2 cell nuclei.

作者信息

Bossart W, Egger D, Rasser Y, Bienz K

出版信息

J Gen Virol. 1982 Nov;63 (Pt 1):131-40. doi: 10.1099/0022-1317-63-1-131.

DOI:10.1099/0022-1317-63-1-131
PMID:6184446
Abstract

Nuclei isolated from uninfected HEp-2 cells synthesized RNA for 60 to 90 min. The individual RNA polymerase activities were determined by alpha-amanitin differential inhibition and the RNA products characterized by electron microscope (EM) autoradiography and sucrose gradient centrifugation. In nuclei prepared from poliovirus-infected cells, the capacity to synthesize RNA in vitro decreased with time after infection. RNA polymerase II activity (hnRNA synthesis) was preferentially inhibited more than was the polymerase I activity (rRNA synthesis). Poliovirus-infected cytoplasm (S-30) inhibited in vitro RNA synthesis in uninfected nuclei by selectively affecting the polymerase II activity. Selective inhibition of hnRNA synthesis by the crude extracts could be monitored by EM autoradiography directly. Determinations of individual RNA polymerase activities by differential alpha-amanitin inhibition were done only after treatment of the infected cytoplasm with micrococcal nuclease to abolish virus RNA replication. Selective inhibition of hnRNA synthesis depended on preincubation of the nuclei together with the infected cytoplasm, indicating that inhibitory substances from the infected cytoplasm entered the nuclei. Isolated nuclei therefore provide a useful system for studying the nature of the inhibitor(s) and of host RNA synthesis inhibition by picornaviruses.

摘要

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引用本文的文献

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Picornaviruses and nuclear functions: targeting a cellular compartment distinct from the replication site of a positive-strand RNA virus.微小核糖核酸病毒与核功能:靶向一个不同于正链RNA病毒复制位点的细胞区室。
Front Microbiol. 2015 Jun 18;6:594. doi: 10.3389/fmicb.2015.00594. eCollection 2015.