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Jung, personal communication. You'll be in good company. Journal of Lipid Research. Previous Section Next Section. Plasmids The cloning strategy employed throughout these studies involved cloning of fragments of interest into several vectors that contain a CpoI site inserted into each polylinker. Immunoprecipitation and Immunoblotting The procedures used have been described In Vitro Histone Binding Binding reactions were carried as described 6 , Previous Section.

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Arad U. Biotechniques 24 , — Yun M. Cell Res. Robin-Lespinasse Y. Cell Sci. Paulette F. Ajithdoss, Lucy F. Reddy Both homo and heterodimers of Marek's disease virus encoded Meq protein contribute to transformation of lymphocytes in chickens. Virology share first authorship. Ellison, Paul A. Thomas J. Ajithdoss, Oren Gilad, Lucy F. Journal of Virology share first authorship. Pei-Ching Chang, Latricia D. Ann, Paul A. Cancer Research Oliver Gautschi, Clifford G. Tepper, Phillip R. Purnell, Yoshihiro Izumiya, Christopher P. Evans, Tim P. Green, Pierre Y.

Desprez, Primo N. Lara, David R. Gandara, Philip C.

Yoshihiro Izumiya D.V.M. Ph.D. - UC Davis Department of Dermatology

Journal of Virology Alon M. Witter, Lucy F. Lee, Carol J. Furthermore, the microPeptide-mediated manipulation of protein function that adds a new dimension of biological regulation is on the horizon Jaber and Yuan, Second, increasing evidence suggests that contributions of KSHV lytic life cycle to oncogenesis are far greater than what we thought before. Is KSHV reactivation and lytic replication required for tumorigenesis by increasing viral titer to facilitate viral dissemination to the sites of tumor? At least 12 KSHV lytic proteins have been demonstrated to involve oncogenesis including transforming, pro-angiogenic, pro-growth, anti-apoptotic, or immuno-modulatory functions.

Do these viral lytic proteins thus serve as direct effectors of the disease phenotypes and do lytically infected cells serve not only as reservoirs of infectious virus but also as reservoirs of pathogenic viral proteins? Research on these questions will provide novel insights into pathogenesis of tumor viruses.

There is currently no definitive cure for KS. Classic cancer therapies are generally used to treat KS patients, which include surgical excision and radiation therapy for patients with a few lesions in a limited area and chemotherapy for patients with extensive or recurrent KS Antman and Chang, However, these therapeutic agents do not target the etiological virus and the tumor response to any chemotherapeutic regimen is only transient.

However, currently there are no effective drugs targeting KSHV available. For example, RTA is unique transcription factor. Its DNA binding region does not contain any well-characterized DNA binding motifs and the overall protein shows no homology with any known cellular transcriptional activators. Therefore, RTA is an attractive target for antiviral therapy. In addition, virion assembly and egress processes are expected to be effective targets for broad-spectrum antiviral drugs.

KA and YY contribute to the writing, figure-making, and proofreading for this review article.

Kaposi Sarcoma Herpesvirus: New Perspectives (Hardcover, 2007 ed.)

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. Aksyuk, A. Subassemblies and asymmetry in assembly of herpes simplex virus procapsid. Anders, D.

Kaposi's Sarcoma-Associated Herpesvirus-Related Solid Lymphoma Involving the Heart and Brain

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KSHV reactivation and novel implications of protein isomerization on lytic switch control. Viruses 7, 72— Gunther, T. The epigenetic landscape of latent Kaposi sarcoma- associated herpesvirus genomes. Guo, H. Open reading frame 33 of a gammaherpesvirus encodes a tegument protein essential for virion morphogenesis and egress. Gwack, Y. Haque, M. Harrington, W. Lancet , — Harrison, S. FEBS Lett. Homa, F. Huang, L. Reciprocal regulatory interaction between human herpesvirus 8 and human immunodeficiency virus type 1. Hyun, T. Iroezindu, M. Health Sci.

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