Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen, Nijmegen, The Netherlands.
PLoS One. 2012;7(2):e31022. doi: 10.1371/journal.pone.0031022. Epub 2012 Feb 17.
MicroRNAs (miRNAs) are important gene regulators that are abundantly expressed in both the developing and adult mammalian brain. These non-coding gene transcripts are involved in post-transcriptional regulatory processes by binding to specific target mRNAs. Approximately one third of known miRNA genes are located within intronic regions of protein coding and non-coding regions, and previous studies have suggested a role for intronic miRNAs as negative feedback regulators of their host genes. In the present study, we monitored the dynamic gene expression changes of the intronic miR-338-3p and miR-338-5p and their host gene Apoptosis-associated Tyrosine Kinase (AATK) during the maturation of rat hippocampal neurons. This revealed an uncorrelated expression pattern of mature miR-338 strands with their host gene. Sequence analysis of the 3' untranslated region (UTR) of rat AATK mRNA revealed the presence of two putative binding sites for miR-338-3p. Thus, miR-338-3p may have the capacity to modulate AATK mRNA levels in neurons. Transfection of miR-338-3p mimics into rat B35 neuroblastoma cells resulted in a significant decrease of AATK mRNA levels, while the transfection of synthetic miR-338-5p mimics did not alter AATK levels. Our results point to a possible molecular mechanism by which miR-338-3p participates in the regulation of its host gene by modulating the levels of AATK mRNA, a kinase which plays a role during differentiation, apoptosis and possibly in neuronal degeneration.
微小 RNA(miRNA)是在发育中和成年哺乳动物脑中大量表达的重要基因调控因子。这些非编码基因转录物通过与特定的靶 mRNA 结合参与转录后调控过程。大约三分之一已知的 miRNA 基因位于蛋白质编码和非编码区域的内含子区域内,先前的研究表明内含子 miRNA 作为其宿主基因的负反馈调节剂发挥作用。在本研究中,我们监测了大鼠海马神经元成熟过程中内含子 miR-338-3p 和 miR-338-5p 及其宿主基因凋亡相关酪氨酸激酶(AATK)的动态基因表达变化。这揭示了成熟 miR-338 链与其宿主基因的表达模式不相关。大鼠 AATK mRNA 的 3'非翻译区(UTR)的序列分析显示存在两个潜在的 miR-338-3p 结合位点。因此,miR-338-3p 可能具有调节神经元中 AATK mRNA 水平的能力。miR-338-3p 模拟物转染大鼠 B35 神经母细胞瘤细胞导致 AATK mRNA 水平显著降低,而合成的 miR-338-5p 模拟物转染则不改变 AATK 水平。我们的结果表明,miR-338-3p 通过调节 AATK mRNA 水平参与其宿主基因的调节的可能分子机制,该激酶在分化、凋亡和可能的神经元退化过程中发挥作用。