Abid Deanna, Murphy Kristin, Murphy Zachary, Rahman Nabil, Getman Michael, Steiner Laurie
Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Department of Biology, St John Fisher University, Rochester, NY 14618, USA.
Development. 2025 May 15;152(10). doi: 10.1242/dev.204485. Epub 2025 May 19.
Erythropoiesis is characterized by dramatic changes in gene expression in the context of a cell that is rapidly proliferating while simultaneously condensing its nucleus in anticipation of enucleation. The mechanisms that maintain high level expression of erythroid genes and promote nuclear condensation remain poorly understood. Condensin II is a ring-like complex that promotes mitotic chromatin condensation and has roles in regulating interphase chromatin architecture and gene expression. We interrogated the role of Condensin II in erythropoiesis using an erythroid-specific deletion of the Condensin II subunit, Ncaph2. Ncaph2 loss resulted in severe anemia by embryonic day 12.5 with embryonic lethality. Ncaph2 mutant erythroid cells had dysregulated maturation and disrupted cell cycle progression, but surprisingly NCAPH2 was dispensable for nuclear condensation. Genomic studies revealed that NCAPH2 occupied the promoter of key erythroid and cell cycle genes that were downregulated following Ncaph2 loss. Together, our results demonstrate an essential role for NCAPH2 in the gene expression programs that regulate cell cycle progression and erythroid differentiation, and identify a role for the Condensin II complex in the regulation of a lineage-specific differentiation program.
红细胞生成的特征是,在一个快速增殖的细胞中,基因表达发生显著变化,同时该细胞会为去核做准备而使细胞核浓缩。维持红细胞基因高水平表达并促进细胞核浓缩的机制仍知之甚少。凝聚素II是一种环状复合物,可促进有丝分裂染色质浓缩,并在调节间期染色质结构和基因表达中发挥作用。我们利用红细胞特异性缺失凝聚素II亚基Ncaph2,研究了凝聚素II在红细胞生成中的作用。Ncaph2缺失导致在胚胎第12.5天出现严重贫血并伴有胚胎致死性。Ncaph2突变的红细胞生成细胞成熟失调且细胞周期进程中断,但令人惊讶的是,NCAPH2对于细胞核浓缩并非必需。基因组研究表明,NCAPH2占据关键红细胞和细胞周期基因的启动子,Ncaph2缺失后这些基因表达下调。总之,我们的结果证明了NCAPH2在调节细胞周期进程和红细胞分化的基因表达程序中起着至关重要的作用,并确定了凝聚素II复合物在调节谱系特异性分化程序中的作用。