UMR 1092, INSERM, CHU Limoges, Université Limoges, F-87000 Limoges, France.
Laboratoire de Bactériologie-Virologie-Hygiène, National Reference Center for Herpesviruses (NRCHV), CHU Limoges, F-87000 Limoges, France.
Viruses. 2019 Nov 26;11(12):1093. doi: 10.3390/v11121093.
The human cytomegalovirus (HCMV) terminase complex is part of DNA-packaging machinery that delivers a unit-length genome into a procapsid. Sequence comparison of herpesvirus homologs allowed us to identify a potential LATLNDIERFL and zinc finger pattern in N-terminal part of pUL56. Recombinant viruses were generated with specific serine or alanine substitutions in these putative patterns. We identified a LATLNDIERFL pattern characteristic of LAGLIDADG homing endonucleases and a metal-binding pattern involving the cysteine and histidine residues C-X2-C-X22-C-X-H (CCCH) close to the region conferring letermovir resistance. These patterns are crucial for viral replication, suggesting that they are essential for pUL56 structure and function. Thus, these patterns represent potential targets for the development of new antivirals such as small molecules or peptides and may allow to better understand the letermovir mechanism of action.
人巨细胞病毒(HCMV)终止酶复合物是将单位长度基因组递送至衣壳的 DNA 包装机制的一部分。疱疹病毒同源物的序列比较使我们能够在 pUL56 的 N 端部分识别出一个潜在的 LATLNDIERFL 和锌指模式。在这些假定的模式中,用特定的丝氨酸或丙氨酸取代产生了重组病毒。我们鉴定了一个 LATLNDIERFL 模式,其特征是 LAGLIDADG 归巢内切核酸酶,以及一个涉及半胱氨酸和组氨酸残基 C-X2-C-X22-C-X-H(CCCH)的金属结合模式,该模式靠近赋予勒特莫韦抗性的区域。这些模式对于病毒复制至关重要,表明它们对于 pUL56 的结构和功能是必不可少的。因此,这些模式代表了开发新抗病毒药物(如小分子或肽)的潜在目标,并可能有助于更好地理解勒特莫韦的作用机制。