Toyoda Masashi, Shirato Haruki, Nakajima Kuniko, Kojima Mizuyo, Takahashi Miho, Kubota Misae, Suzuki-Migishima Rika, Motegi Yoshiko, Yokoyama Minesuke, Takeuchi Takashi
Mitsubishi Kagaku Institute of Life Sciences (MITILS), 11 Minamiooya, Machida, 194-8511, Tokyo, .
Dev Cell. 2003 Jul;5(1):85-97. doi: 10.1016/s1534-5807(03)00189-8.
Spatiotemporal regulation of cell proliferation is necessary for normal tissue development. The molecular mechanisms, especially the signaling pathways controlling the cell cycle machinery, remain largely unknown. Here, we demonstrate a negative relationship between the spatiotemporal patterns of jumonji (jmj) expression and cardiac myocyte proliferation. cyclin D1 expression and cell proliferation are enhanced in the cardiac myocytes of jmj-deficient mutant embryos. In contrast, jmj overexpression represses cyclin D1 expression in cardiac cells, and Jmj protein binds to cyclin D1 promoter in vivo and represses its transcriptional activity. cyclin D1 overexpression causes hyperproliferation in the cardiac myocytes, but the absence of cyclin D1 in jmj mutant embryos rescues the hyperproliferation. Therefore, Jmj might control cardiac myocyte proliferation and consequently cardiac morphogenesis by repressing cyclin D1 expression.
细胞增殖的时空调节对于正常组织发育是必要的。其分子机制,尤其是控制细胞周期机制的信号通路,在很大程度上仍然未知。在这里,我们证明了jumonji(jmj)表达的时空模式与心肌细胞增殖之间存在负相关关系。在jmj缺陷突变胚胎的心肌细胞中,细胞周期蛋白D1表达和细胞增殖增强。相反,jmj过表达抑制心脏细胞中的细胞周期蛋白D1表达,并且Jmj蛋白在体内与细胞周期蛋白D1启动子结合并抑制其转录活性。细胞周期蛋白D1过表达导致心肌细胞过度增殖,但jmj突变胚胎中细胞周期蛋白D1的缺失挽救了过度增殖。因此,Jmj可能通过抑制细胞周期蛋白D1表达来控制心肌细胞增殖,进而控制心脏形态发生。