Buck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945-1400, USA.
IMBA, Dr. Bohrgasse 3, 1030 Vienna, Austria.
Cell Rep. 2017 Sep 12;20(11):2527-2537. doi: 10.1016/j.celrep.2017.08.059.
Sophisticated mechanisms that preserve genome integrity are critical to ensure the maintenance of regenerative capacity while preventing transformation of somatic stem cells (SCs), yet little is known about mechanisms regulating genome maintenance in these cells. Here, we show that intestinal stem cells (ISCs) induce the Argonaute family protein Piwi in response to JAK/STAT signaling during acute proliferative episodes. Piwi function is critical to ensure heterochromatin maintenance, suppress retrotransposon activation, and prevent DNA damage in homeostasis and under regenerative pressure. Accordingly, loss of Piwi results in the loss of actively dividing ISCs and their progenies by apoptosis. We further show that Piwi expression is sufficient to allay age-related retrotransposon expression, DNA damage, apoptosis, and mis-differentiation phenotypes in the ISC lineage, improving epithelial homeostasis. Our data identify a role for Piwi in the regulation of somatic SC function, and they highlight the importance of retrotransposon control in somatic SC maintenance.
复杂的机制可以保护基因组的完整性,对于确保在防止体细胞干细胞(SCs)转化的同时保持其再生能力至关重要,但关于调节这些细胞中基因组维持的机制知之甚少。在这里,我们发现肠道干细胞(ISCs)在急性增殖期响应 JAK/STAT 信号诱导 Argonaute 家族蛋白 Piwi。Piwi 的功能对于维持异染色质、抑制逆转录转座子的激活以及在体内平衡和再生压力下防止 DNA 损伤至关重要。因此,Piwi 的缺失会导致活跃分裂的 ISC 及其通过细胞凋亡而产生的后代的丢失。我们进一步表明,Piwi 的表达足以缓解 ISC 谱系中与年龄相关的逆转录转座子表达、DNA 损伤、细胞凋亡和分化错误表型,从而改善上皮细胞的体内平衡。我们的数据确定了 Piwi 在调节体细胞干细胞功能中的作用,并强调了逆转录转座子控制在体细胞干细胞维持中的重要性。