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KSHV Encoded LANA Recruits Nucleosome Assembly Protein NAP1L1 for Regulating Viral DNA Replication and Transcription

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Journal Sci Rep
Specialty Science
Date 2016 Sep 8
PMID 27599637
Citations 10
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Abstract

The establishment of latency is an essential for lifelong persistence and pathogenesis of Kaposi's sarcoma-associated herpesvirus (KSHV). Latency-associated nuclear antigen (LANA) is the most abundantly expressed protein during latency and is important for viral genome replication and transcription. Replication-coupled nucleosome assembly is a major step in packaging the newly synthesized DNA into chromatin, but the mechanism of KSHV genome chromatinization post-replication is not understood. Here, we show that nucleosome assembly protein 1-like protein 1 (NAP1L1) associates with LANA. Our binding assays revealed an association of LANA with NAP1L1 in KSHV-infected cells, which binds through its amino terminal domain. Association of these proteins confirmed their localization in specific nuclear compartments of the infected cells. Chromatin immunoprecipitation assays from NAP1L1-depleted cells showed LANA-mediated recruitment of NAP1L1 at the terminal repeat (TR) region of the viral genome. Presence of NAP1L1 stimulated LANA-mediated DNA replication and persistence of a TR-containing plasmid. Depletion of NAP1L1 led to a reduced nucleosome positioning on the viral genome. Furthermore, depletion of NAP1L1 increased the transcription of viral lytic genes and overexpression decreased the promoter activities of LANA-regulated genes. These results confirmed that LANA recruitment of NAP1L1 helps in assembling nucleosome for the chromatinization of newly synthesized viral DNA.

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References
1.
Ballestas M, Kaye K . The latency-associated nuclear antigen, a multifunctional protein central to Kaposi's sarcoma-associated herpesvirus latency. Future Microbiol. 2011; 6(12):1399-413. PMC: 3857968. DOI: 10.2217/fmb.11.137. View

2.
Wei F, Gan J, Wang C, Zhu C, Cai Q . Cell Cycle Regulatory Functions of the KSHV Oncoprotein LANA. Front Microbiol. 2016; 7:334. PMC: 4811921. DOI: 10.3389/fmicb.2016.00334. View

3.
Attia M, Forster A, Rachez C, Freemont P, Avner P, Christine Rogner U . Interaction between nucleosome assembly protein 1-like family members. J Mol Biol. 2011; 407(5):647-60. DOI: 10.1016/j.jmb.2011.02.016. View

4.
Clark J, Alvarez D, Alexeyev M, King J, Huang L, Yoder M . Regulatory role for nucleosome assembly protein-1 in the proliferative and vasculogenic phenotype of pulmonary endothelium. Am J Physiol Lung Cell Mol Physiol. 2007; 294(3):L431-9. DOI: 10.1152/ajplung.00316.2007. View

5.
Friborg Jr J, Kong W, Hottiger M, Nabel G . p53 inhibition by the LANA protein of KSHV protects against cell death. Nature. 2000; 402(6764):889-94. DOI: 10.1038/47266. View