Department of Biology, Indiana University, Bloomington, IN 47405, USA.
Department of Biology, Indiana University, Bloomington, IN 47405, USA.
Cell Rep. 2022 Oct 18;41(3):111495. doi: 10.1016/j.celrep.2022.111495.
Somatic adult stem cell lineages in high-turnover tissues are under tight gene regulatory control. Like its mammalian counterpart, the Drosophila intestine precisely adjusts the rate of stem cell division with the onset of differentiation based on physiological demand. Although Notch signaling is indispensable for these decisions, the regulation of Notch activity that drives the differentiation of stem cell progenies into functional, mature cells is not well understood. Here, we report that commitment to the terminally differentiated enterocyte (EC) cell fate is under microRNA control. We show that an intestinally enriched microRNA, miR-956, fine-tunes Notch signaling activity specifically in intermediate, enteroblast (EB) progenitor cells to control EC differentiation. We further identify insensitive mRNA as a target of miR-956 that regulates EB/EC ratios by repressing Notch activity in EBs. In summary, our study highlights a post-transcriptional gene-regulatory mechanism for controlling differentiation in an adult intestinal stem cell lineage.
高度分化组织中的体干细胞谱系受到严格的基因调控控制。与哺乳动物对应物一样,果蝇肠道根据生理需求,在分化开始时精确地调整干细胞分裂的速度。尽管 Notch 信号对于这些决定是必不可少的,但驱动干细胞后代分化为功能性成熟细胞的 Notch 活性的调节尚不清楚。在这里,我们报告说,向终末分化的肠细胞(EC)命运的决定受到 microRNA 的控制。我们表明,一种在肠道中丰富的 microRNA,miR-956,精细地调节 Notch 信号活性,专门在中间的肠母细胞(EB)祖细胞中控制 EC 分化。我们进一步鉴定出不敏感 mRNA 作为 miR-956 的靶标,通过在 EBs 中抑制 Notch 活性来调节 EB/EC 比。总之,我们的研究强调了一种转录后基因调控机制,用于控制成年肠道干细胞谱系中的分化。