Graduate School of Life Science, Hokkaido University, Japan.
Graduate School of Life Science, Hokkaido University, Japan; Faculty of Advanced Life Science, Hokkaido University, Japan.
Biochem Biophys Res Commun. 2018 Sep 26;504(1):231-237. doi: 10.1016/j.bbrc.2018.08.160. Epub 2018 Sep 5.
Near-haploidy is observed in certain cancer types, but ploidy-dependent alterations in gene regulation in the haploid state remain elusive. Here, by comparative transcriptome analysis between human isogenic haploid and diploid cell lines, we found lowering of cyclin D2 level in haploids. Acute genome duplication in haploids restored cyclin D2 expression to diploid level, indicating that the regulation of cyclin D2 expression is directly linked to ploidy. Downstream pathways of cyclin D2, such as Rb phosphorylation and p27 sequestration remained intact in haploids, suggesting that they adapt to lowered cyclin D level. Interestingly, however, haploid cells were more susceptible to cdk4/6 inhibition compared to diploids. Our finding indicates feasibility of selective growth suppression of haploid cells based on ploidy-linked gene regulation.
在某些癌症类型中观察到近单体性,但单体状态下依赖于倍性的基因调控改变仍难以捉摸。在这里,通过对人同基因单体和二倍体细胞系之间的比较转录组分析,我们发现单体中的细胞周期蛋白 D2 水平降低。单体中的急性基因组加倍将细胞周期蛋白 D2 的表达恢复到二倍体水平,表明细胞周期蛋白 D2 表达的调节直接与倍性相关。细胞周期蛋白 D2 的下游途径,如 Rb 磷酸化和 p27 隔离在单体中仍然完整,表明它们适应了降低的细胞周期蛋白 D 水平。然而,有趣的是,与二倍体相比,单体细胞对 CDK4/6 抑制更敏感。我们的发现表明,基于与倍性相关的基因调控,选择性抑制单体细胞生长是可行的。