Department of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Cell Rep. 2013 Jun 27;3(6):2100-12. doi: 10.1016/j.celrep.2013.05.038. Epub 2013 Jun 20.
Expression of microRNAs (miRNAs) involves transcription of miRNA genes and maturation of the primary transcripts. Recent studies have shown that posttranscriptional processing of primary and precursor miRNAs is induced after DNA damage through regulatory RNA-binding proteins in the Drosha and Dicer complexes, such as DDX5 and KSRP. However, little is known about the regulation of nuclear export of pre-miRNAs in the DNA-damage response, a critical step in miRNA maturation. Here, we show that nuclear export of pre-miRNAs is accelerated after DNA damage in an ATM-dependent manner. The ATM-activated AKT kinase phosphorylates Nup153, a key component of the nucleopore, leading to enhanced interaction between Nup153 and Exportin-5 (XPO5) and increased nuclear export of pre-miRNAs. These findings define an important role of DNA-damage signaling in miRNA transport and maturation.
miRNAs 的表达涉及 miRNA 基因的转录和初级转录本的成熟。最近的研究表明,在 DNA 损伤后,通过 Drosha 和 Dicer 复合物中的调节 RNA 结合蛋白(如 DDX5 和 KSRP),初级和前体 miRNA 的转录后加工被诱导。然而,对于 DNA 损伤反应中 pre-miRNA 的核输出调控知之甚少,这是 miRNA 成熟的关键步骤。在这里,我们表明 pre-miRNA 的核输出在 ATM 依赖性方式下在 DNA 损伤后被加速。ATM 激活的 AKT 激酶使核孔的关键组成部分 Nup153 磷酸化,导致 Nup153 与 Exportin-5(XPO5)之间的相互作用增强,从而增加 pre-miRNA 的核输出。这些发现定义了 DNA 损伤信号在 miRNA 运输和成熟中的重要作用。