复制因子C
原点识别复合体
生物
染色体复制控制
复制前复合体
微小染色体维持
真核细胞DNA复制
SeqA蛋白质结构域
DNA复制
DNA复制因子CDT1
病毒复制
Ter蛋白
许可因素
复制的起源
遗传学
细胞生物学
dnaB解旋酶
解旋酶
聚合酶
病毒学
脱氧核糖核酸
DNA
病毒进化
复制蛋白A
作者
Nicole Boisvert,Stephanie Thurmond,Carmen M. Elenberger,Patricio Jeraldo,Cato Prince,Nolan Sutherland,José Iranildo Miranda De Melo,Ken Tsheowang,Cameron Dodier,Maciej T. Nogalski,Dinesh Verma,Geoffrey Parsons,Joseph Cabral
标识
DOI:10.1073/pnas.2516306122
摘要
Anelloviridae is a family of single-stranded DNA viruses that are thought to be nonpathogenic and commensal. Despite their ubiquitous presence in human populations, little is known about the anellovirus mechanism of replication in host cells. We identified the protein coded by ORF2/3 as necessary and sufficient to initiate replication from the minimal origin of replication for viruses of both the Beta- and Alphatorquevirus genera. Supporting this observation, we identified components of the polymerase alpha and BTR (Bloom’s syndrome helicase (BLM), topoisomerase IIIα, RMI1, and RMI2) complexes as interacting with the viral replication initiation protein (Rip) during DNA replication, suggesting a recombination-dependent mechanism of replication that uses host cell machinery to mediate dissolution of replication intermediates. Furthermore, we mapped a 92-bp minimal origin of replication sequence for the Betatorquevirus genus composed of an adenine and thymine (AT)-rich stretch and a portion of the guanine and cytosine (GC)-rich region. Altogether, this study provides insight into the mechanism by which anelloviruses manipulate host cell machinery to facilitate viral genome replication and represents a significant step forward in understanding the complex processes underlying anellovirus replication and persistent infection of these important commensal viruses.
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