Caro Elena, Gutierrez Crisanto
Centro de Biologia Molecular "Severo Ochoa", Consejo Superior de Investigaciones Cientificas, Universidad Autonoma de Madrid, Cantoblanco, 28049 Madrid, Spain.
Trends Cell Biol. 2007 Dec;17(12):580-5. doi: 10.1016/j.tcb.2007.09.008. Epub 2007 Nov 9.
The transition of precursor cells from an undifferentiated proliferative state to differentiated cells with specific fates is of primary importance for multicellular organisms. Animals and plants have evolved two unrelated proteins, geminin and GEM, respectively, that play analogous roles in regulating this transition. These proteins are involved, probably in early G1 phase of the cell cycle, in regulating the expression of genes involved in cell fate and initiation of differentiation. They also interact with Cdt1, a component of the pre-replication complexes involved in DNA replication licensing in early G1 phase. The interaction of geminin and GEM with Cdt1 and transcriptional regulators is competitive, suggesting that these interactions can play a pivotal role in coordinating DNA replication, cell division and cell fate decisions.
前体细胞从未分化的增殖状态转变为具有特定命运的分化细胞,这对多细胞生物至关重要。动物和植物分别进化出了两种不相关的蛋白质,即双微体蛋白和GEM,它们在调节这种转变中发挥着类似的作用。这些蛋白质可能在细胞周期的G1早期阶段,参与调节与细胞命运和分化起始相关的基因表达。它们还与Cdt1相互作用,Cdt1是参与G1早期DNA复制许可的前复制复合物的一个组成部分。双微体蛋白和GEM与Cdt1及转录调节因子的相互作用是竞争性的,这表明这些相互作用在协调DNA复制、细胞分裂和细胞命运决定方面可能起着关键作用。