首页> 美国卫生研究院文献>The EMBO Journal >Poliovirus proteinase 3C converts an active form of transcription factor IIIC to an inactive form: a mechanism for inhibition of host cell polymerase III transcription by poliovirus.
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Poliovirus proteinase 3C converts an active form of transcription factor IIIC to an inactive form: a mechanism for inhibition of host cell polymerase III transcription by poliovirus.

机译:脊髓灰质炎病毒蛋白酶3C将活性形式的转录因子IIIC转化为非活性形式:一种通过脊髓灰质炎病毒抑制宿主细胞聚合酶III转录的机制。

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摘要

In HeLa cells, RNA polymerase III (pol III)-mediated transcription is severely inhibited by poliovirus infection. This is due primarily to a reduction in the transcriptional activity of TFIIIC, a transcription factor which binds in a sequence specific manner to the internal promoter of pol III genes. Using gel retardation assays, we have shown previously that inhibition of pol III transcription by poliovirus is correlated with disappearance of a transcriptionally active form of TFIIIC (complex I) concomitant with the appearance of a faster mobility, transcriptionally inactive form of TFIIIC (complex III). We show here that a poliovirus with a point mutation in the proteinase 3C (3Cpro) region failed to produce complex III and is limited in its ability to inhibit pol III transcription compared with the wild-type virus. Incubation of purified 3Cpro, expressed in Escherichia coli, with transcriptionally active TFIIIC (complex I) in vitro resulted in generation of the transcriptionally inactive complex III form of TFIIIC. In an in vitro transcription assay, treatment of the complex I form of TFIIIC with 3Cpro almost completely inhibited pol III transcription. Finally expression of the 3Cpro gene in transfected HeLa cells resulted in significant inhibition of pol III-mediated transcription. The results presented here suggest that proteolysis of the transcriptionally active form of TFIIIC by poliovirus 3Cpro is a mechanism by which poliovirus inhibits host cell RNA pol III transcription.
机译:在HeLa细胞中,脊髓灰质炎病毒感染严重抑制了RNA聚合酶III(pol III)介导的转录。这主要是由于TFIIIC的转录活性降低,TFIIIC是一种以序列特异性方式与pol III基因的内部启动子结合的转录因子。使用凝胶阻滞分析,我们先前已证明脊髓灰质炎病毒对pol III转录的抑制与TFIIIC(复合体I)的转录活性形式消失,伴随着TFIIIC(复合体III)的更快迁移性,转录失活形式的出现有关。我们在这里显示,脊髓灰质炎病毒在蛋白酶3C(3Cpro)区中具有点突变,未能产生复合物III,与野生型病毒相比,其抑制pol III转录的能力受到限制。在大肠杆菌中表达的纯化3Cpro与转录活性TFIIIC(复合体I)在体外孵育,导致生成了TFIIIC转录无活性的复合体III形式。在体外转录测定中,用3Cpro处理TFIIIC的I型复合物几乎完全抑制了pol III转录。最后,在转染的HeLa细胞中3Cpro基因的表达导致pol III介导的转录的显着抑制。此处显示的结果表明,脊髓灰质炎病毒3Cpro对TFIIIC转录活性形式的蛋白水解是脊髓灰质炎病毒抑制宿主细胞RNA pol III转录的机制。

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