Department of Molecular Genetics, 1 Kings College Circle, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
Virology. 2011 Jun 5;414(2):119-29. doi: 10.1016/j.virol.2011.03.013. Epub 2011 Apr 13.
The human cytomegalovirus (HCMV) UL35 gene encodes two proteins, UL35 and UL35a. Expression of UL35 in transfected cells results in the formation of UL35 nuclear bodies that associate with promyelocytic leukemia (PML) protein. PML forms the basis for PML nuclear bodies that are important for suppressing viral lytic gene expression. Given the important relationship between PML and viral infection, we have further investigated the association of UL35 with PML bodies. We demonstrate that UL35 bodies form independently of PML and subsequently recruit PML, Sp100 and Daxx. In contrast, UL35a did not form bodies; however, it could bind UL35 and inhibit the formation of UL35 bodies. The HCMV tegument protein pp71 promoted the formation of UL35 bodies and the cytoplasmic localization of UL35a. Similarly, UL35a shifted pp71 to the cytoplasm. These results indicate that the interplay between UL35, UL35a and pp71 affects their subcellular localization and likely their functions throughout infection.
人类巨细胞病毒 (HCMV) 的 UL35 基因编码两种蛋白质,即 UL35 和 UL35a。在转染细胞中表达 UL35 会导致 UL35 核体的形成,该核体与早幼粒细胞白血病 (PML) 蛋白相关联。PML 是 PML 核体的基础,对于抑制病毒裂解基因的表达非常重要。鉴于 PML 与病毒感染之间的重要关系,我们进一步研究了 UL35 与 PML 体的关联。我们证明 UL35 体的形成独立于 PML,随后招募 PML、Sp100 和 Daxx。相比之下,UL35a 不会形成体;然而,它可以结合 UL35 并抑制 UL35 体的形成。HCMV 包膜蛋白 pp71 促进 UL35 体的形成和 UL35a 的细胞质定位。同样,UL35a 将 pp71 转移到细胞质中。这些结果表明,UL35、UL35a 和 pp71 之间的相互作用影响它们的亚细胞定位,可能影响它们在整个感染过程中的功能。