Tada T, Tada M
Department of Development and Differentiation, Institute for Frontier Medical Sciences, Kyoto University, Japan.
Cell Struct Funct. 2001 Jun;26(3):149-60. doi: 10.1247/csf.26.149.
The recent fascinating breakthrough in the area of stem cell research is the successful production of cloned animals via nuclear transplantation of somatic nucleus by intrinsic trans-acting factors of oocytes and trans-differentiation of somatic stem cells from adult organs induced by extrinsic growth factors. During the process of nuclear reprogramming, epigenetic modification of the somatic nuclei must be achieved to acquire toti-/pluripotential competence. However, the molecular mechanism involved is largely unknown. It has been shown that DNA methylation, histone acetylation and chromatin structure are involved in the establishment of epigenetic modification. Now it is evident that they function cooperatively to establish and maintain active or inactive chromatin state. Here we discuss the mechanisms of epigenetic modification potentially involved in the event of nuclear reprogramming.
干细胞研究领域最近一项引人入胜的突破是,通过卵母细胞的内在反式作用因子对体细胞核进行核移植,以及由外在生长因子诱导成体器官的体干细胞进行转分化,成功培育出了克隆动物。在核重编程过程中,必须实现体细胞核的表观遗传修饰,以获得全能/多能能力。然而,其中涉及的分子机制在很大程度上尚不清楚。研究表明,DNA甲基化、组蛋白乙酰化和染色质结构参与了表观遗传修饰的建立。现在很明显,它们协同作用以建立和维持活跃或不活跃的染色质状态。在此,我们讨论核重编程过程中可能涉及的表观遗传修饰机制。