Vana Marcy L, Tang Yi, Chen Aiping, Medina Gisselle, Carter Carol, Leis Jonathan
Department of Microbiology and Immunology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Ave., Chicago, IL 60611, USA.
J Virol. 2004 Dec;78(24):13943-53. doi: 10.1128/JVI.78.24.13943-13953.2004.
Rous sarcoma virus (RSV) budding requires an interaction of the L domain within the p2b region of Gag with cellular Nedd4-family E3 ubiquitin protein ligases. Members of our laboratories previously demonstrated that overexpression of a fragment of the chicken Nedd4-like protein (LDI-1 WW) inhibits Gag release in a dominant-negative manner (A. Kikonyogo, F. Bouamr, M. L. Vana, Y. Xiang, A. Aiyar, C. Carter, and J. Leis, Proc. Natl. Acad. Sci. USA 98:11199-11204, 2001). We have now identified the complete 3' end of LDI-1 and determined that it has a C-terminal ubiquitin ligase HECT domain, similar to other Nedd4 family members. While overexpression of the full-length LDI-1 clone (LDI-1 FL) had little effect on Gag budding, an LDI-1 FL mutant with a substitution in the HECT domain catalytic site blocked Gag release, similar to LDI-1 WW. The coexpression of Gag and hemagglutinin-tagged ubiquitin (HA-Ub) resulted in the detection of mono- and polyubiquitinated forms of Gag in cells and mostly monoubiquitinated Gag in virus-like particles (VLPs). When the Nedd4-binding site (L domain) was deleted, ubiquitinated Gag was not detected. Interestingly, the release of Gag with ubiquitin covalently linked to the C terminus (Gag-Ub) was still blocked by LDI-1 WW. To understand the mechanism of this inhibition, we examined cells expressing Gag and LDI-1 WW by electron microscopy. In the presence of LDI-1 WW, VLPs were found in electron-dense inclusion bodies in the cytoplasm of transfected cells. In contrast, when cells that coexpressed Gag-Ub and LDI-1 WW were examined, inclusion bodies were detected but did not contain VLPs. These results indicate that the ubiquitination of Gag is dependent upon Nedd4 binding to the L domain and suggest that Nedd4 has additional functions during RSV release besides the ubiquitination of Gag.
劳氏肉瘤病毒(RSV)出芽需要Gag蛋白p2b区域内的L结构域与细胞Nedd4家族E3泛素蛋白连接酶相互作用。我们实验室的成员之前证明,鸡Nedd4样蛋白片段(LDI-1 WW)的过表达以显性负性方式抑制Gag释放(A. Kikonyogo、F. Bouamr、M. L. Vana、Y. Xiang、A. Aiyar、C. Carter和J. Leis,《美国国家科学院院刊》98:11199 - 11204,2001)。我们现已鉴定出LDI-1完整的3'末端,并确定它具有C末端泛素连接酶HECT结构域,这与其他Nedd4家族成员相似。虽然全长LDI-1克隆(LDI-1 FL)的过表达对Gag出芽影响不大,但在HECT结构域催化位点有替代的LDI-1 FL突变体却能阻断Gag释放,这与LDI-1 WW类似。Gag与血凝素标记的泛素(HA-Ub)共表达导致在细胞中检测到单泛素化和多泛素化形式的Gag,而在病毒样颗粒(VLP)中大多检测到单泛素化的Gag。当Nedd4结合位点(L结构域)缺失时,未检测到泛素化的Gag。有趣的是,与泛素共价连接到C末端的Gag(Gag-Ub)的释放仍被LDI-1 WW阻断。为了解这种抑制的机制,我们通过电子显微镜检查了表达Gag和LDI-1 WW的细胞。在存在LDI-1 WW的情况下,在转染细胞的细胞质中电子致密的包涵体中发现了VLP。相反,当检查共表达Gag-Ub和LDI-1 WW的细胞时,检测到了包涵体,但其中不含VLP。这些结果表明,Gag的泛素化依赖于Nedd4与L结构域的结合,并提示Nedd4在RSV释放过程中除了Gag的泛素化外还具有其他功能。