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CHD3 facilitates vRNP nuclear export by interacting with NES1 of influenza A virus NS2

机译:CHD3通过与甲型流感病毒NS2的NES1相互作用促进vRNP核出口

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摘要

NS2 from influenza A virus mediates Crm1-dependent vRNP nuclear export through interaction with Crm1. However, even though the nuclear export signal 1 (NES1) of NS2 does not play a requisite role in NS2–Crm1 interaction, there is no doubt that NES1 is crucial for vRNP nuclear export. While the mechanism of the NES1 is still unclear, it is speculated that certain host partners might mediate the NES1 function through their interaction with NES1. In the present study, chromodomain-helicase-DNA-binding protein 3 (CHD3) was identified as a novel host nuclear protein for locating NS2 and Crm1 on dense chromatin for NS2 and Crm1-dependent vRNP nuclear export. CHD3 was confirmed to interact with NES1 in NS2, and a disruption to this interaction by mutation in NES1 significantly delayed viral vRNPs export and viral propagation. Further, the knockdown of CHD3 would affect the propagation of the wild-type virus but not the mutant with the weakened NS2–CHD3 interaction. Therefore, this study demonstrates that NES1 is required for maximal binding of NS2 to CHD3, and that the NS2–CHD3 interaction on the dense chromatin contributed to the NS2-mediated vRNP nuclear export.Electronic supplementary materialThe online version of this article (doi:10.1007/s00018-014-1726-9) contains supplementary material, which is available to authorized users.
机译:甲型流感病毒的NS2通过与Crm1相互作用介导Crm1依赖性vRNP核输出。但是,即使NS2的核出口信号1(NES1)在NS2–Crm1相互作用中不发挥必不可少的作用,毫无疑问NES1对于vRNP核出口至关重要。虽然尚不清楚NES1的机制,但推测某些宿主伙伴可能通过与NES1的相互作用来介导NES1的功能。在本研究中,染色体域-解旋酶-DNA结合蛋白3(CHD3)被确定为一种新型宿主核蛋白,用于将NS2和Crm1定位在致密染色质上,用于NS2和Crm1依赖性vRNP核输出。 CHD3被证实与NS2中的NES1相互作用,并且由于NES1突变而对该相互作用的破坏显着延迟了病毒vRNP的输出和病毒繁殖。此外,敲低CHD3会影响野生型病毒的传播,但不会影响NS2-CHD3相互作用减弱的突变体。因此,这项研究表明NES1是NS2与CHD3的最大结合所必需的,并且致密染色质上NS2–CHD3的相互作用有助于NS2介导的vRNP核输出。电子补充材料本文的在线版本(doi:10.1007) / s00018-014-1726-9)包含补充材料,授权用户可以使用。

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