Wang Xiaoli, Lybarger Lonnie, Connors Rose, Harris Michael R, Hansen Ted H
Department of Pathology and Immunology, Box 8118, Washington University School of Medicine, 4566 Scott Ave., St. Louis, MO 63110, USA.
J Virol. 2004 Aug;78(16):8673-86. doi: 10.1128/JVI.78.16.8673-8686.2004.
The mK3 protein of gammaherpesvirus 68 and the kK5 protein of Kaposi's sarcoma-associated herpesvirus are members of a family of structurally related viral immune evasion molecules that all possess a RING-CH domain with ubiquitin ligase activity. These proteins modulate the expression of major histocompatibility complex class I molecules (mK3 and kK5) as well as other molecules like ICAM-1 and B7.2 (kK5). Previously, mK3 was shown to ubiquitinate nascent class I molecules, resulting in their rapid degradation, and this process was found to be dependent on TAP and tapasin, endoplasmic reticulum molecules involved in class I assembly. Here, we demonstrate that in murine cells, kK5 does not affect class I expression but does downregulate human B7.2 molecules in a TAP/tapasin-independent manner. These differences in substrate specificity and TAP/tapasin dependence between mK3 and kK5 permitted us, using chimeric molecules, to map the sites of mK3 interaction with TAP/tapasin and to determine the requirements for substrate recognition by mK3. Our findings indicate that mK3 interacts with TAP1 and -2 via their C-terminal domains and with class I molecules via their N-terminal domains. Furthermore, by orienting the RING-CH domain of mK3 appropriately with respect to class I, mK3 binding to TAP/tapasin, rather than the presence of unique sequences in class I, appears to be the primary determinant of substrate specificity.
γ疱疹病毒68的mK3蛋白和卡波西肉瘤相关疱疹病毒的kK5蛋白是结构相关的病毒免疫逃避分子家族的成员,这些分子都具有带有泛素连接酶活性的RING-CH结构域。这些蛋白可调节主要组织相容性复合体I类分子(mK3和kK5)以及其他分子如细胞间黏附分子-1(ICAM-1)和B7.2(kK5)的表达。此前研究表明,mK3可使新生的I类分子泛素化,导致其快速降解,且该过程依赖于抗原加工相关转运体(TAP)和tapasin,这两种内质网分子参与I类分子组装。在此,我们证明在鼠细胞中,kK5不影响I类分子表达,但能以不依赖TAP/tapasin的方式下调人B7.2分子。mK3和kK5在底物特异性和对TAP/tapasin的依赖性上的这些差异,使我们能够利用嵌合分子确定mK3与TAP/tapasin相互作用的位点,并确定mK3识别底物的要求。我们的研究结果表明,mK3通过其C末端结构域与TAP1和TAP2相互作用,并通过其N末端结构域与I类分子相互作用。此外,通过使mK3的RING-CH结构域相对于I类分子适当地定向,mK3与TAP/tapasin的结合,而非I类分子中独特序列的存在,似乎是底物特异性的主要决定因素。