Large Scale RNAi Reveals the Requirement of Nuclear Envelope Breakdown for Nuclear Import of Human Papillomaviruses

被引:123
作者
Aydin, Inci [1 ,2 ]
Weber, Susanne [1 ,2 ]
Snijder, Berend [3 ]
Ventayol, Pilar Samperio [1 ,2 ]
Kuehbacher, Andreas [4 ]
Becker, Miriam [1 ,2 ]
Day, Patricia M. [5 ]
Schiller, John T. [5 ]
Kann, Michael [6 ]
Pelkmans, Lucas [3 ]
Helenius, Ari [4 ]
Schelhaas, Mario [1 ,2 ]
机构
[1] Univ Munster, ZMBE, Inst Mol Virol & Med Biochem, Emmy Noether Grp Virus Endocytosis, D-48149 Munster, Germany
[2] Cluster Excellence EXC1003, Munster, Germany
[3] Univ Zurich, Inst Mol Life Sci, Zurich, Switzerland
[4] ETH, Inst Biochem, Zurich, Switzerland
[5] NCI, Cellular Oncol Lab, NIH, Bethesda, MD 20892 USA
[6] Univ Bordeaux Segalen, Lab Microbiol Fondamentale & Pathogenicite, Bordeaux, France
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
MINOR CAPSID PROTEIN; VIRUS-LIKE PARTICLES; SMALL-MOLECULE INHIBITOR; HEPARAN-SULFATE; MONOCLONAL-ANTIBODIES; HUMAN KERATINOCYTES; ALPHA(6) INTEGRIN; CELLULAR ENTRY; VIRAL-DNA; INFECTION;
D O I
10.1371/journal.ppat.1004162
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A two-step, high-throughput RNAi silencing screen was used to identify host cell factors required during human papillomavirus type 16 (HPV16) infection. Analysis of validated hits implicated a cluster of mitotic genes and revealed a previously undetermined mechanism for import of the viral DNA (vDNA) into the nucleus. In interphase cells, viruses were endocytosed, routed to the perinuclear area, and uncoated, but the vDNA failed to be imported into the nucleus. Upon nuclear envelope perforation in interphase cells HPV16 infection occured. During mitosis, the vDNA and L2 associated with host cell chromatin on the metaphase plate. Hence, we propose that HPV16 requires nuclear envelope breakdown during mitosis for access of the vDNA to the nucleoplasm. The results accentuate the value of genes found by RNAi screens for investigation of viral infections. The list of cell functions required during HPV16 infection will, moreover, provide a resource for future virus-host cell interaction studies.
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页数:19
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