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微小RNA生物合成与核转运的动力学

Dynamics of miRNA biogenesis and nuclear transport.

作者信息

Kotipalli Aneesh, Gutti Ravikumar, Mitra Chanchal K

机构信息

Department of Biochemistry, School of Life Sciences, University of Hyderabad, Hyderabad 500046, http://www.uohyd.ac.in/ India.

出版信息

J Integr Bioinform. 2017 Apr 20;13(5):22-34. doi: 10.1515/jib-2016-305.

Abstract

MicroRNAs (miRNAs) are short noncoding RNA sequences ~22 nucleotides in length that play an important role in gene regulation-transcription and translation. The processing of these miRNAs takes place in both the nucleus and the cytoplasm while the final maturation occurs in the cytoplasm. Some mature miRNAs with nuclear localisation signals (NLS) are transported back to the nucleus and some remain in the cytoplasm. The functional roles of these miRNAs are seen in both the nucleus and the cytoplasm. In the nucleus, miRNAs regulate gene expression by binding to the targeted promoter sequences and affect either the transcriptional gene silencing (TGS) or transcriptional gene activation (TGA). In the cytoplasm, targeted mRNAs are translationally repressed or cleaved based on the complementarity between the two sequences at the seed region of miRNA and mRNA. The selective transport of mature miRNAs to the nucleus follows the classical nuclear import mechanism. The classical nuclear import mechanism is a highly regulated process, involving exportins and importins. The nuclear pore complex (NPC) regulates all these transport events like a gate keeper. The half-life of miRNAs is rather low, so within a short time miRNAs perform their function. Temporal studies of miRNA biogenesis are, therefore, useful. We have carried out simulation studies for important miRNA biogenesis steps and also classical nuclear import mechanism using ordinary differential equation (ODE) solver in the Octave software.

摘要

微小RNA(miRNA)是长度约为22个核苷酸的短非编码RNA序列,在基因调控(转录和翻译)中发挥重要作用。这些miRNA的加工过程在细胞核和细胞质中均会发生,而最终成熟过程在细胞质中进行。一些具有核定位信号(NLS)的成熟miRNA会被转运回细胞核,而一些则保留在细胞质中。这些miRNA的功能作用在细胞核和细胞质中均有体现。在细胞核中,miRNA通过与靶向启动子序列结合来调控基因表达,并影响转录基因沉默(TGS)或转录基因激活(TGA)。在细胞质中,基于miRNA种子区域与mRNA两个序列之间的互补性,靶向mRNA会被翻译抑制或切割。成熟miRNA向细胞核的选择性转运遵循经典的核输入机制。经典的核输入机制是一个高度受调控的过程,涉及输出蛋白和输入蛋白。核孔复合体(NPC)像门卫一样调控所有这些转运事件。miRNA的半衰期相当短,因此miRNA能在短时间内发挥其功能。所以,对miRNA生物发生进行时间研究是有用的。我们使用八度软件中的常微分方程(ODE)求解器,对重要的miRNA生物发生步骤以及经典的核输入机制进行了模拟研究。

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