Anastasakis Dimitrios, Skeparnias Ilias, Shaukat Athanasios-Nasir, Grafanaki Katerina, Kanellou Alexandra, Taraviras Stavros, Papachristou Dionysios J, Papakyriakou Athanasios, Stathopoulos Constantinos
Department of Biochemistry, School of Medicine, University of Patras, 26504 Rio Achaia, Greece.
Department of Physiology, School of Medicine, University of Patras, 26504 Rio Achaia, Greece.
Nucleic Acids Res. 2016 Oct 14;44(18):8908-8920. doi: 10.1093/nar/gkw709. Epub 2016 Aug 11.
PNLDC1 is a homologue of poly(A) specific ribonuclease (PARN), a known deadenylase with additional role in processing of non-coding RNAs. Both enzymes were reported recently to participate in piRNA biogenesis in silkworm and C. elegans, respectively. To get insights on the role of mammalian PNLDC1, we characterized the human and mouse enzymes. PNLDC1 shows limited conservation compared to PARN and represents an evolutionary related but distinct group of enzymes. It is expressed specifically in mouse embryonic stem cells, human and mouse testes and during early mouse embryo development, while it fades during differentiation. Its expression in differentiated cells, is suppressed through methylation of its promoter by the de novo methyltransferase DNMT3B. Both enzymes are localized mainly in the ER and exhibit in vitro specificity restricted solely to 3' RNA or DNA polyadenylates. Knockdown of Pnldc1 in mESCs and subsequent NGS analysis showed that although the expression of the remaining deadenylases remains unaffected, it affects genes involved mainly in reprogramming, cell cycle and translational regulation. Mammalian PNLDC1 is a novel deadenylase expressed specifically in cell types which share regulatory mechanisms required for multipotency maintenance. Moreover, it could be involved both in posttranscriptional regulation through deadenylation and genome surveillance during early development.
PNLDC1是聚(A)特异性核糖核酸酶(PARN)的同源物,PARN是一种已知的去腺苷酸化酶,在非编码RNA的加工中具有额外作用。最近报道这两种酶分别参与家蚕和秀丽隐杆线虫中的piRNA生物合成。为了深入了解哺乳动物PNLDC1的作用,我们对人和小鼠的这种酶进行了表征。与PARN相比,PNLDC1的保守性有限,代表了一组进化相关但不同的酶。它在小鼠胚胎干细胞、人和小鼠睾丸以及小鼠胚胎早期发育过程中特异性表达,而在分化过程中逐渐消失。它在分化细胞中的表达通过从头甲基转移酶DNMT3B对其启动子的甲基化而受到抑制。这两种酶主要定位于内质网,并且在体外仅对3' RNA或DNA聚腺苷酸具有特异性。在小鼠胚胎干细胞中敲低Pnldc1并随后进行NGS分析表明,尽管其余去腺苷酸化酶的表达不受影响,但它影响主要参与重编程、细胞周期和翻译调控的基因。哺乳动物PNLDC1是一种新型去腺苷酸化酶,在具有维持多能性所需调控机制的细胞类型中特异性表达。此外,它可能既参与通过去腺苷酸化的转录后调控,又参与早期发育过程中的基因组监测。