Conveniently, the microRNA that targets t antigen is made late in the infectious cycle, just when t antigen is no longer essential for virus replication.
以t抗原为攻击目标的小分子rna在感染周期的最后环节才会产生，而这时t抗原已经不再是病毒繁殖的必须条件。
The pre-replication complex (Pre-RC) forms in late mitosis/early G1 phase beginning with the binding of CDT1 and cdc6 to the origin, which allows binding of the heterohexameric MCM2-7 complex.
前复制复合体（Pre-RC）在有丝分裂末期/G1早期随着CDT1和cdc6的结合而形成，允许异源六聚化的MCM2-7复合体的结合。
The pre-replication complex (Pre-RC) forms in late mitosis/early G1 phase beginning with the binding of CDT1 and cdc6 to the origin, which allows binding of the heterohexameric MCM2-7 complex.
前复制复合体（Pre-RC）在有丝分裂末期/G1早期随着CDT1和cdc6的结合而形成，允许异源六聚化的MCM2-7复合体的结合。
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