Bray Samantha, Turnbull Matthew, Hebert Sherry, Douville Renée N
Douville Lab, Department of Biology, University of Winnipeg, Winnipeg MB, Canada.
Douville Lab, Department of Biology, University of Winnipeg, WinnipegMB, Canada; Department of Immunology, University of Manitoba, WinnipegMB, Canada.
Front Microbiol. 2016 Dec 1;7:1941. doi: 10.3389/fmicb.2016.01941. eCollection 2016.
Retroviruses create permanently integrated proviruses that exist in the host genome. Retroviral genomes encode for functionally conserved , and regions, as well as integrase (IN), which is required for retroviral integration. IN mediates viral genome insertion through 3' end processing of the viral DNA and the strand transfer reaction. This process requires the formation of a pre-integration complex, comprised of IN, viral DNA, and cellular proteins. Viral insertion causes DNA damage, leading to the requirement of host DNA repair mechanisms. Therefore, a failure of DNA repair pathways may result in genomic instability and potentially cause host cell death. Considering the numerous human diseases associated with genomic instability, the endogenous retrovirus-K (ERVK) IN should be considered as a putative contributor to DNA damage in human cells. Future research and drug discovery should focus on ERVK IN activity and its role in human conditions, such as neurological disease and cancers.
逆转录病毒会产生永久整合的原病毒,这些原病毒存在于宿主基因组中。逆转录病毒基因组编码功能保守的区域以及整合酶(IN),逆转录病毒整合需要整合酶。整合酶通过病毒DNA的3'末端加工和链转移反应介导病毒基因组插入。这个过程需要形成一个由整合酶、病毒DNA和细胞蛋白组成的预整合复合体。病毒插入会导致DNA损伤,从而需要宿主DNA修复机制。因此,DNA修复途径的失败可能导致基因组不稳定,并可能导致宿主细胞死亡。鉴于许多人类疾病与基因组不稳定有关,内源性逆转录病毒K(ERVK)整合酶应被视为人类细胞中DNA损伤的一个假定因素。未来的研究和药物研发应聚焦于ERVK整合酶的活性及其在人类疾病(如神经疾病和癌症)中的作用。