Developmental Biology, Department of Biology, Faculty of Sciences, Utrecht University, Padualaan 8, 3584 CH Utrecht, the Netherlands.
Developmental Biology, Department of Biology, Faculty of Sciences, Utrecht University, Padualaan 8, 3584 CH Utrecht, the Netherlands.
Cell. 2015 Jul 16;162(2):300-313. doi: 10.1016/j.cell.2015.06.013. Epub 2015 Jul 2.
The transition from proliferating precursor cells to post-mitotic differentiated cells is crucial for development, tissue homeostasis, and tumor suppression. To study cell-cycle exit during differentiation in vivo, we developed a conditional knockout and lineage-tracing system for Caenorhabditis elegans. Combined lineage-specific gene inactivation and genetic screening revealed extensive redundancies between previously identified cell-cycle inhibitors and the SWI/SNF chromatin-remodeling complex. Muscle precursor cells missing either SWI/SNF or G1/S inhibitor function could still arrest cell division, while simultaneous inactivation of these regulators caused continued proliferation and a C. elegans tumor phenotype. Further genetic analyses support that SWI/SNF acts in concert with hlh-1 MyoD, antagonizes Polycomb-mediated transcriptional repression, and suppresses cye-1 Cyclin E transcription to arrest cell division of muscle precursors. Thus, SWI/SNF and G1/S inhibitors provide alternative mechanisms to arrest cell-cycle progression during terminal differentiation, which offers insight into the frequent mutation of SWI/SNF genes in human cancers.
从增殖前体细胞向有丝分裂后分化细胞的转变对于发育、组织稳态和肿瘤抑制至关重要。为了研究体内分化过程中的细胞周期退出,我们开发了一种用于秀丽隐杆线虫的条件性基因敲除和谱系追踪系统。结合谱系特异性基因失活和遗传筛选,揭示了先前鉴定的细胞周期抑制剂与 SWI/SNF 染色质重塑复合物之间存在广泛的冗余性。缺失 SWI/SNF 或 G1/S 抑制剂功能的肌肉前体细胞仍然可以停止细胞分裂,而这些调节剂的同时失活会导致持续增殖和秀丽隐杆线虫肿瘤表型。进一步的遗传分析支持 SWI/SNF 与 hlh-1 MyoD 协同作用,拮抗 Polycomb 介导的转录抑制,并抑制 cye-1 Cyclin E 的转录,从而阻止肌肉前体细胞的细胞分裂。因此,SWI/SNF 和 G1/S 抑制剂在终末分化过程中提供了阻止细胞周期进程的替代机制,这为人类癌症中 SWI/SNF 基因的频繁突变提供了深入了解。