The Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS One. 2013;8(1):e53512. doi: 10.1371/journal.pone.0053512. Epub 2013 Jan 9.
Epstein-Barr virus (EBV) is a gammaherpesvirus that causes infectious mononucleosis, B cell lymphomas, and nasopharyngeal carcinoma. Many of the genes required for EBV virion morphogenesis are found in all herpesviruses, but some are specific to gammaherpesviruses. One of these gamma-specific genes, BLRF2, encodes a tegument protein that has been shown to be essential for replication in other gammaherpesviruses. In this study, we identify BLRF2 interacting proteins using binary and co-complex protein assays. Serine/Arginine-rich Protein Kinase 2 (SRPK2) was identified by both assays and was further shown to phosphorylate an RS motif in the BLRF2 C-terminus. Mutation of this RS motif (S148A+S150A) abrogated the ability of BLRF2 to support replication of a murine gammaherpesvirus 68 genome lacking the BLRF2 homolog (ORF52). We conclude that the BLRF2 RS motif is phosphorylated by SRPK2 and is important for viral replication.
EB 病毒(EBV)是一种γ疱疹病毒,可引起传染性单核细胞增多症、B 细胞淋巴瘤和鼻咽癌。 EBV 病毒粒子形态发生所需的许多基因在所有疱疹病毒中都有发现,但有些基因是γ疱疹病毒所特有的。这些γ特异性基因之一,BLRF2,编码一种被膜蛋白,已被证明在其他γ疱疹病毒的复制中是必不可少的。在这项研究中,我们使用二元和共复合物蛋白测定法来鉴定 BLRF2 的相互作用蛋白。丝氨酸/精氨酸丰富蛋白激酶 2(SRPK2)被这两种测定法都鉴定出来,并进一步被证明磷酸化 BLRF2 C 末端的 RS 基序。该 RS 基序(S148A+S150A)的突变消除了 BLRF2 支持缺乏 BLRF2 同源物(ORF52)的小鼠γ疱疹病毒 68 基因组复制的能力。我们的结论是,BLRF2 的 RS 基序被 SRPK2 磷酸化,对于病毒复制很重要。