CAS Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Core Facility for Protein Research, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Protein Cell. 2018 Oct;9(10):848-866. doi: 10.1007/s13238-017-0480-9. Epub 2017 Sep 26.
Aberrant regulation of miRNA genes contributes to pathogenesis of a wide range of human diseases, including cancer. The TAR DNA binding protein 43 (TDP-43), a RNA/DNA binding protein associated with neurodegeneration, is involved in miRNA biogenesis. Here, we systematically examined miRNAs regulated by TDP-43 using RNA-Seq coupled with an siRNA-mediated knockdown approach. TDP-43 knockdown affected the expression of a number of miRNAs. In addition, TDP-43 down-regulation led to alterations in the patterns of different isoforms of miRNAs (isomiRs) and miRNA arm selection, suggesting a previously unknown role of TDP-43 in miRNA processing. A number of TDP-43 associated miRNAs, and their candidate target genes, are associated with human cancers. Our data reveal highly complex roles of TDP-43 in regulating different miRNAs and their target genes. Our results suggest that TDP-43 may promote migration of lung cancer cells by regulating miR-423-3p. In contrast, TDP-43 increases miR-500a-3p expression and binds to the mature miR-500a-3p sequence. Reduced expression of miR-500a-3p is associated with poor survival of lung cancer patients, suggesting that TDP-43 may have a suppressive role in cancer by regulating miR-500a-3p. Cancer-associated genes LIF and PAPPA are possible targets of miR-500a-3p. Our work suggests that TDP-43-regulated miRNAs may play multifaceted roles in the pathogenesis of cancer.
miRNA 基因的异常调控导致广泛的人类疾病的发病机制,包括癌症。与神经退行性变相关的 RNA/DNA 结合蛋白 TAR DNA 结合蛋白 43(TDP-43)参与 miRNA 的生物发生。在这里,我们使用 RNA-Seq 结合 siRNA 介导的敲低方法系统地检查了受 TDP-43 调节的 miRNA。TDP-43 敲低影响了许多 miRNA 的表达。此外,TDP-43 的下调导致不同 miRNA 同工型(isomiRs)和 miRNA 臂选择模式的改变,表明 TDP-43 在 miRNA 加工中具有未知的作用。许多与 TDP-43 相关的 miRNA 及其候选靶基因与人类癌症有关。我们的数据揭示了 TDP-43 在调节不同 miRNA 及其靶基因方面的高度复杂作用。我们的结果表明,TDP-43 可能通过调节 miR-423-3p 来促进肺癌细胞的迁移。相比之下,TDP-43 增加了 miR-500a-3p 的表达并与成熟的 miR-500a-3p 序列结合。miR-500a-3p 的表达减少与肺癌患者的不良生存相关,表明 TDP-43 通过调节 miR-500a-3p 可能在癌症中发挥抑制作用。癌症相关基因 LIF 和 PAPPA 可能是 miR-500a-3p 的靶基因。我们的工作表明,TDP-43 调节的 miRNA 可能在癌症的发病机制中发挥多方面的作用。