State Key Laboratory of Silkworm Genome Biology, Biological Science Research Center, Southwest University, Chongqing 400715, China.
Chongqing Key Laboratory of Sericultural Science, Chongqing engineering and technology research center for novel silk materials, Southwest University, Chongqing 400715, China.
Nucleic Acids Res. 2020 May 7;48(8):4214-4229. doi: 10.1093/nar/gkaa158.
Endoreplication, known as endocycle, is a variant of the cell cycle that differs from mitosis and occurs in specific tissues of different organisms. Endoreplicating cells generally undergo multiple rounds of genome replication without chromosome segregation. Previous studies demonstrated that Drosophila fizzy-related protein (Fzr) and its mammalian homolog Cdh1 function as key regulators of endoreplication entrance by activating the anaphase-promoting complex/cyclosome to initiate the ubiquitination and subsequent degradation of cell cycle factors such as Cyclin B (CycB). However, the molecular mechanism underlying Fzr-mediated endoreplication is not completely understood. In this study, we demonstrated that the transcription factor Myc acts downstream of Fzr during endoreplication in Drosophila salivary gland. Mechanistically, Fzr interacts with chromatin-associated histone H2B to enhance H2B ubiquitination in the Myc promoter and promotes Myc transcription. In addition to negatively regulating CycB transcription, the Fzr-ubiquitinated H2B (H2Bub)-Myc signaling cascade also positively regulates the transcription of the MCM6 gene that is involved in DNA replication by directly binding to specific motifs within their promoters. We further found that the Fzr-H2Bub-Myc signaling cascade regulating endoreplication progression is conserved between insects and mammalian cells. Altogether, our work uncovers a novel transcriptional cascade that is involved in Fzr-mediated endoreplication.
内复制,也称为内周期,是细胞周期的一种变体,与有丝分裂不同,发生在不同生物体的特定组织中。内复制细胞通常经历多次基因组复制而没有染色体分离。先前的研究表明,果蝇 fizzy-related 蛋白(Fzr)及其哺乳动物同源物 Cdh1 通过激活后期促进复合物/周期蛋白来启动细胞周期因子如 Cyclin B(CycB)的泛素化和随后的降解,从而作为内复制进入的关键调节剂。然而,Fzr 介导的内复制的分子机制尚不完全清楚。在这项研究中,我们证明了转录因子 Myc 在果蝇唾液腺的内复制过程中是 Fzr 的下游靶标。在机制上,Fzr 与染色质相关的组蛋白 H2B 相互作用,以增强 Myc 启动子中的 H2B 泛素化,并促进 Myc 转录。除了负调控 CycB 转录外,Fzr-泛素化的 H2B(H2Bub)-Myc 信号级联还通过直接结合其启动子内的特定基序,正调控参与 DNA 复制的 MCM6 基因的转录。我们进一步发现,昆虫和哺乳动物细胞之间内复制进展的 Fzr-H2Bub-Myc 信号级联是保守的。总之,我们的工作揭示了一种新的转录级联,它参与了 Fzr 介导的内复制。