Sasiprapa KhunchaiMutita JunkingAroonroong SuttitheptumrongUmpa YasamutNunghathai SawasdeeJanjuree NetsawangAtthapan MorchangPrapaipit ChaowalitSansanee NoisakranPa thai YenchitsomanusThawornchai LimjindapornFaculty of Medicine, Siriraj Hospital, Mahidol UniversityMahidol UniversityRangsit UniversityThailand National Center for Genetic Engineering and Biotechnology2018-06-112018-06-112012-06-29Biochemical and Biophysical Research Communications. Vol.423, No.2 (2012), 398-403109021040006291X2-s2.0-84862861520https://repository.li.mahidol.ac.th/handle/20.500.14594/13691Dengue fever (DF), dengue hemorrhagic fever (DHF), and dengue shock syndrome (DSS), caused by dengue virus (DENV) infection, are important public health problems in the tropical and subtropical regions. Abnormal hemostasis and plasma leakage are the main patho-physio logical changes in DHF/DSS. A remarkably increased production of cytokines, the so called 'cytokine storm', is observed in the patients with DHF/DSS. A complex interaction between DENV proteins and the host immune response contributes to cytokine production. However, the molecular mechanism(s) by which DENV nonstructural protein 5 (NS5) mediates these responses has not been fully elucidated. In the present study, yeast two-hybrid assay was performed to identify host proteins interacting with DENV NS5 and a death-domain-associate protein (Daxx) was identified. The in vivo relevance of this interaction was suggested by co-immunoprecipitation and nuclear co-localization of these two proteins in HEK293 cells expressing DENV NS5. HEK293 cells expressing DENV NS5-K/A, which were mutated at the nuclear localization sequences (NLS), were created to assess its functional roles in nuclear translocation, Daxx interaction, and cytokine production. In the absence of NLS, DENV NS5 could neither translocate into the nucleus nor interact with Daxx to increase the DHF-associated cytokine, RANTES (CCL5) production. This work demonstrates the interaction between DENV NS5 and Daxx and the role of the interaction on the modulation of RANTES production. © 2012 Elsevier Inc.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyArticleSCOPUS10.1016/j.bbrc.2012.05.137