Grammatikakis Ioannis, Gorospe Myriam
Laboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD 21224, USA.
Stem Cell Investig. 2016 Apr 7;3:10. doi: 10.21037/sci.2016.03.05. eCollection 2016.
Splicing increases immensely the complexity of gene products expressed in the cell. The precise regulation of splicing is critical for the development, homeostasis, and function of all tissues in the body, including those comprising the neural system. Ramos et al. recently identified Pnky as a long noncoding RNA expressed selectively in neural tissues that was implicated in the transition of neural stem cells (NSCs) to mature neurons. Pnky actions appeared to be mediated by its interaction with the splicing factor and RNA-binding protein (RBP) polypyrimidine tract-binding protein (PTBP1), as silencing either Pnky or PTBP1 modulated in similar ways the patterns of spliced and expressed mRNAs in the cell. Strikingly, lowering the expression levels of Pnky or PTBP1 in NSCs actually enhanced neurogenesis, suggesting that the Pnky-PTBP1 complex elicited a splicing program of suppression of neurogenesis. With rapid progress in the design and delivery of RNA-based therapies, interventions to reduce Pnky levels may prove beneficial towards enhancing neurogenesis in disease states characterized by aberrant neuronal loss.
剪接极大地增加了细胞中表达的基因产物的复杂性。剪接的精确调控对于身体所有组织(包括构成神经系统的组织)的发育、稳态和功能至关重要。拉莫斯等人最近确定Pnky是一种在神经组织中选择性表达的长链非编码RNA,它与神经干细胞(NSC)向成熟神经元的转变有关。Pnky的作用似乎是通过其与剪接因子和RNA结合蛋白(RBP)多嘧啶序列结合蛋白(PTBP1)的相互作用来介导的,因为沉默Pnky或PTBP1会以类似的方式调节细胞中剪接和表达的mRNA模式。引人注目的是,降低神经干细胞中Pnky或PTBP1的表达水平实际上增强了神经发生,这表明Pnky-PTBP1复合物引发了一个抑制神经发生的剪接程序。随着基于RNA的疗法在设计和递送方面的快速进展,降低Pnky水平的干预措施可能被证明有助于在以异常神经元丢失为特征的疾病状态下增强神经发生。