Systematic identification of cellular signals reactivating Kaposi sarcoma-associated herpesvirus.
Yu, Fuqu, Harada, Josephine, Brown, Helen J, Deng, Hongyu, Song, Moon Jung, Wu, Ting-Ting, Kato-Stankiewicz, Juran, Nelson, Christian G, Vieira, Jeffrey, Tamanoi, Fuyuhiko, Chanda, Sumit and Sun, Ren (2007) Systematic identification of cellular signals reactivating Kaposi sarcoma-associated herpesvirus. PLoS Pathogens, 3 (3). e44. ISSN 1553-7374
Abstract
The herpesvirus life cycle has two distinct phases: latency and lytic replication. The balance between these two phases is critical for viral pathogenesis. It is believed that cellular signals regulate the switch from latency to lytic replication. To systematically evaluate the cellular signals regulating this reactivation process in Kaposi sarcoma-associated herpesvirus, the effects of 26,000 full-length cDNA expression constructs on viral reactivation were individually assessed in primary effusion lymphoma-derived cells that harbor the latent virus. A group of diverse cellular signaling proteins were identified and validated in their effect of inducing viral lytic gene expression from the latent viral genome. The results suggest that multiple cellular signaling pathways can reactivate the virus in a genetically homogeneous cell population. Further analysis revealed that the Raf/MEK/ERK/Ets-1 pathway mediates Ras-induced reactivation. The same pathway also mediates spontaneous reactivation, which sets the first example to our knowledge of a specific cellular pathway being studied in the spontaneous reactivation process. Our study provides a functional genomic approach to systematically identify the cellular signals regulating the herpesvirus life cycle, thus facilitating better understanding of a fundamental issue in virology and identifying novel therapeutic targets.
Item Type: | Article |
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Date Deposited: | 13 Oct 2015 13:17 |
Last Modified: | 13 Oct 2015 13:17 |
URI: | https://oak.novartis.com/id/eprint/88 |