Choksi Semil P, Southall Tony D, Bossing Torsten, Edoff Karin, de Wit Elzo, Fischer Bettina E, van Steensel Bas, Micklem Gos, Brand Andrea H
The Gurdon Institute and Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.
Dev Cell. 2006 Dec;11(6):775-89. doi: 10.1016/j.devcel.2006.09.015.
Stem cells have the remarkable ability to give rise to both self-renewing and differentiating daughter cells. Drosophila neural stem cells segregate cell-fate determinants from the self-renewing cell to the differentiating daughter at each division. Here, we show that one such determinant, the homeodomain transcription factor Prospero, regulates the choice between stem cell self-renewal and differentiation. We have identified the in vivo targets of Prospero throughout the entire genome. We show that Prospero represses genes required for self-renewal, such as stem cell fate genes and cell-cycle genes. Surprisingly, Prospero is also required to activate genes for terminal differentiation. We further show that in the absence of Prospero, differentiating daughters revert to a stem cell-like fate: they express markers of self-renewal, exhibit increased proliferation, and fail to differentiate. These results define a blueprint for the transition from stem cell self-renewal to terminal differentiation.
干细胞具有产生自我更新和分化子代细胞的非凡能力。果蝇神经干细胞在每次分裂时都会将细胞命运决定因子从自我更新细胞分离到分化子代细胞中。在这里,我们表明,这样一种决定因子,即同源结构域转录因子Prospero,调节干细胞自我更新和分化之间的选择。我们已经在整个基因组中鉴定出Prospero在体内的靶点。我们表明Prospero抑制自我更新所需的基因,如干细胞命运基因和细胞周期基因。令人惊讶的是,Prospero也是激活终末分化基因所必需的。我们进一步表明,在没有Prospero的情况下,分化子代细胞会恢复到类似干细胞的命运:它们表达自我更新标记,增殖增加,并且无法分化。这些结果定义了从干细胞自我更新到终末分化转变的蓝图。