| Literature DB >> 29116593 |
Shujuan Jiang1,2, Yujing Huang1, Ying Qi1, Rong He3, Zhongyang Liu1, Yanping Ma1, Xin Guo1, Yaozhong Shao1, Zhengrong Sun1, Qiang Ruan4.
Abstract
Viruses commonly create favorable cellular conditions for their survival through multiple mechanisms. MicroRNAs (miRNAs), which function as post-transcriptional regulators, are utilized by human cytomegalovirus (HCMV) in its infection and pathogenesis. In the present study, the DNA replication inhibitor Geminin (GMNN) was identified to be a direct target of hcmv-miR-US5-1. Overexpression of hcmv-miR-US5-1 could block the accumulation of GMNN during HCMV infection, and the decrease of GMNN expression caused by hcmv-miR-US5-1 or GMNN specific siRNA reduced HCMV DNA copies in U373 cells. Meanwhile, ectopic expression of hcmv-miR-US5-1 and consequent lower expression of GMNN influenced host cell cycle and proliferation. These results imply that hcmv-miR-US5-1 may affect viral replication and host cellular environment by regulating expression kinetics of GMNN during HCMV infection.Entities:
Keywords: DNA replication; Geminin (GMNN); Human cytomegalovirus (HCMV); cell cycle; hcmv-miR-US5-1
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Year: 2017 PMID: 29116593 PMCID: PMC6598906 DOI: 10.1007/s12250-017-4064-x
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327