Department of Basic Medicine, Hebei North University, Zhangjiakou 075029, China.
Department of Pharmacy, Hebei North University, Zhangjiakou 075029, China.
J Zhejiang Univ Sci B. 2018;19(4):293-304. doi: 10.1631/jzus.B1700179.
Axon regeneration is crucial for recovery from neurological diseases. Numerous studies have identified several genes, microRNAs (miRNAs), and transcription factors (TFs) that influence axon regeneration. However, the regulatory networks involved have not been fully elucidated. In the present study, we analyzed a regulatory network of 51 miRNAs, 27 TFs, and 59 target genes, which is involved in axon regeneration. We identified 359 pairs of feed-forward loops (FFLs), seven important genes (Nap1l1, Arhgef12, Sema6d, Akt3, Trim2, Rab11fip2, and Rps6ka3), six important miRNAs (hsa-miR-204-5p, hsa-miR-124-3p, hsa-miR-26a-5p, hsa-miR-16-5p, hsa-miR-17-5p, and hsa-miR-15b-5p), and eight important TFs (Smada2, Fli1, Wt1, Sp6, Sp3, Smad4, Smad5, and Creb1), which appear to play an important role in axon regeneration. Functional enrichment analysis revealed that axon-associated genes are involved mainly in the regulation of cellular component organization, axonogenesis, and cell morphogenesis during neuronal differentiation. However, these findings need to be validated by further studies.
轴突再生对于神经疾病的康复至关重要。许多研究已经确定了一些基因、microRNAs (miRNAs) 和转录因子 (TFs),它们影响轴突再生。然而,涉及的调控网络尚未完全阐明。在本研究中,我们分析了一个涉及轴突再生的 51 个 miRNA、27 个 TFs 和 59 个靶基因的调控网络。我们鉴定了 359 对前馈回路 (FFLs)、七个重要基因 (Nap1l1、Arhgef12、Sema6d、Akt3、Trim2、Rab11fip2 和 Rps6ka3)、六个重要 miRNA (hsa-miR-204-5p、hsa-miR-124-3p、hsa-miR-26a-5p、hsa-miR-16-5p、hsa-miR-17-5p 和 hsa-miR-15b-5p) 和八个重要 TFs (Smada2、Fli1、Wt1、Sp6、Sp3、Smad4、Smad5 和 Creb1),它们似乎在轴突再生中起着重要作用。功能富集分析表明,轴突相关基因主要参与神经元分化过程中细胞成分组织、轴突发生和细胞形态发生的调节。然而,这些发现需要进一步的研究来验证。