Institute for Physiological Chemistry, Biochemical-Pharmacological Center Marburg, Philipps-University of Marburg, Marburg, Germany.
Lab of Systems Neuroscience, Institute for Neuroscience, Department of Health Science and Technology, Swiss Federal Institute of Technology ETH, Zurich, Switzerland.
RNA Biol. 2021 Sep;18(9):1252-1264. doi: 10.1080/15476286.2020.1830553. Epub 2020 Oct 23.
SYNCRIP, a member of the cellular heterogeneous nuclear ribonucleoprotein (hnRNP) family of RNA binding proteins, regulates various aspects of neuronal development and plasticity. Although SYNCRIP has been identified as a component of cytoplasmic RNA granules in dendrites of mammalian neurons, only little is known about the specific SYNCRIP target mRNAs that mediate its effect on neuronal morphogenesis and function. Here, we present a comprehensive characterization of the cytoplasmic SYNCRIP mRNA interactome using iCLIP in primary rat cortical neurons. We identify hundreds of SYNCRIP target mRNAs, many of which encode for proteins involved in neurogenesis, neuronal migration and neurite outgrowth. From our analysis, the stabilization of mRNAs encoding for components of the microtubule network, such as doublecortin (Dcx), emerges as a novel mechanism of SYNCRIP function in addition to the previously reported control of actin dynamics. Furthermore, we found that SYNCRIP synergizes with pro-neural miRNAs, such as miR-9. Thus, SYNCRIP appears to promote early neuronal differentiation by a two-tier mechanism involving the stabilization of pro-neural mRNAs by direct 3'UTR interaction and the repression of anti-neural mRNAs in a complex with neuronal miRISC. Together, our findings provide a rationale for future studies investigating the function of SYNCRIP in mammalian brain development and disease.
SYNCRIP 是细胞异质核核糖核蛋白 (hnRNP) 家族的 RNA 结合蛋白成员之一,调节神经元发育和可塑性的各个方面。虽然 SYNCRIP 已被鉴定为哺乳动物神经元树突细胞质 RNA 颗粒的组成部分,但对于介导其对神经元形态发生和功能影响的特定 SYNCRIP 靶 mRNA 知之甚少。在这里,我们使用 iCLIP 在原代大鼠皮质神经元中对细胞质 SYNCRIP mRNA 相互作用组进行了全面表征。我们鉴定了数百个 SYNCRIP 靶 mRNA,其中许多编码参与神经发生、神经元迁移和神经突生长的蛋白质。从我们的分析中,除了先前报道的对肌动蛋白动力学的控制外,微管网络成分 mRNA 的稳定作为 SYNCRIP 功能的新机制出现,例如双皮质蛋白 (Dcx)。此外,我们发现 SYNCRIP 与神经前体 miRNA(如 miR-9)协同作用。因此,SYNCRIP 似乎通过涉及通过直接 3'UTR 相互作用稳定神经前体 mRNA 以及与神经元 miRISC 复合物中抑制抗神经 mRNA 的两级机制来促进早期神经元分化。总之,我们的发现为未来研究 SYNCRIP 在哺乳动物大脑发育和疾病中的功能提供了依据。