Craven R C, Leure-duPree A E, Weldon R A, Wills J W
Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey 17033, USA.
J Virol. 1995 Jul;69(7):4213-27. doi: 10.1128/JVI.69.7.4213-4227.1995.
The mature cores of all retroviruses contain a major structural protein known as the CA (capsid) protein. Although it appears to form a shell around the ribonucleoprotein complex that contains the viral RNA, its function in viral replication is largely unknown. Little sequence similarity exists between the CA proteins of different retroviruses, except for a region of about 20 amino acids termed the major homology region (MHR). To examine the role of the CA protein in particle assembly and release, mutants of Rous sarcoma virus were created in which segments of CA were deleted or single conserved residues in the MHR were altered. The ability of the deletion mutants to release particles at rates similar to the wild-type protein demonstrated that the CA domain of Gag is not an essential component of the minimal budding machinery. Certain point mutations in the MHR region did block assembly and release in certain cell types, presumably by perturbing the global structure of the Gag precursor. Another group of MHR substitutions produced noninfectious or poorly infectious particles that were normal in their content of gag and pol gene products and viral RNA. The mutants were capable of initiating reverse transcription in vitro; however, the association of CA protein with the core was compromised, as indicated by its sensitivity to extraction with nonionic detergent. Prominent blebs on the virion envelope also indicated a disturbance at the membrane. Finally, an anti-peptide serum directed against MHR was found to react with the uncleaved Gag protein but not with mature CA, suggesting that MHR undergoes a dynamic rearrangement upon liberation from the polyprotein. We conclude that the MHR is involved in the very late steps in maturation of the virion (i.e., ones that occur after budding is initiated) and is essential for proper function of the core upon entry into a new host cell.
所有逆转录病毒的成熟核心都含有一种主要结构蛋白,称为衣壳(CA)蛋白。尽管它似乎在包含病毒RNA的核糖核蛋白复合体周围形成一个外壳,但其在病毒复制中的功能很大程度上尚不清楚。不同逆转录病毒的CA蛋白之间几乎没有序列相似性,除了一个约20个氨基酸的区域,称为主要同源区域(MHR)。为了研究CA蛋白在病毒粒子组装和释放中的作用,构建了劳斯肉瘤病毒的突变体,其中CA的片段被删除或MHR中的单个保守残基被改变。缺失突变体以与野生型蛋白相似的速率释放病毒粒子的能力表明,Gag的CA结构域不是最小出芽机制的必需成分。MHR区域的某些点突变确实在某些细胞类型中阻断了组装和释放,推测是通过扰乱Gag前体的整体结构。另一组MHR替代产生了无感染性或感染性很差的病毒粒子,其gag和pol基因产物以及病毒RNA的含量正常。这些突变体能够在体外启动逆转录;然而,CA蛋白与核心的结合受到损害,这通过其对非离子去污剂提取的敏感性表明。病毒粒子包膜上突出的泡也表明膜上存在干扰。最后,发现一种针对MHR的抗肽血清与未切割的Gag蛋白反应,但不与成熟的CA反应,这表明MHR从多蛋白中释放后会发生动态重排。我们得出结论,MHR参与病毒粒子成熟的非常晚期步骤(即出芽开始后发生的步骤),并且对于核心进入新宿主细胞后的正常功能至关重要。