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通过整合RNA测序和降解组分析鉴定地钱多形苔中的微小RNA及其靶标

Identification of miRNAs and Their Targets in the Liverwort Marchantia polymorpha by Integrating RNA-Seq and Degradome Analyses.

作者信息

Lin Pin-Chun, Lu Chia-Wei, Shen Bing-Nan, Lee Guan-Zong, Bowman John L, Arteaga-Vazquez Mario A, Liu Li-Yu Daisy, Hong Syuan-Fei, Lo Chu-Fang, Su Gong-Min, Kohchi Takayuki, Ishizaki Kimitsune, Zachgo Sabine, Althoff Felix, Takenaka Mizuki, Yamato Katsuyuki T, Lin Shih-Shun

机构信息

Institute of Biotechnology, National Taiwan University, Taipei, Taiwan 106 These authors contributed equally to this work.

Institute of Biotechnology, National Taiwan University, Taipei, Taiwan 106.

出版信息

Plant Cell Physiol. 2016 Feb;57(2):339-58. doi: 10.1093/pcp/pcw020. Epub 2016 Feb 9.

Abstract

Bryophytes (liverworts, hornworts and mosses) comprise the three earliest diverging lineages of land plants (embryophytes). Marchantia polymorpha, a complex thalloid Marchantiopsida liverwort that has been developed into a model genetic system, occupies a key phylogenetic position. Therefore, M. polymorpha is useful in studies aiming to elucidate the evolution of gene regulation mechanisms in plants. In this study, we used computational, transcriptomic, small RNA and degradome analyses to characterize microRNA (miRNA)-mediated pathways of gene regulation in M. polymorpha. The data have been integrated into the open access ContigViews-miRNA platform for further reference. In addition to core components of the miRNA pathway, 129 unique miRNA sequences, 11 of which could be classified into seven miRNA families that are conserved in embryophytes (miR166a, miR390, miR529c, miR171-3p, miR408a, miR160 and miR319a), were identified. A combination of computational and degradome analyses allowed us to identify and experimentally validate 249 targets. In some cases, the target genes are orthologous to those of other embryophytes, but in other cases, the conserved miRNAs target either paralogs or members of different gene families. In addition, the newly discovered Mpo-miR11707.1 and Mpo-miR11707.2 are generated from a common precursor and target MpARGONAUTE1 (LW1759). Two other newly discovered miRNAs, Mpo-miR11687.1 and Mpo-miR11681.1, target the MADS-box transcription factors MpMADS1 and MpMADS2, respectively. Interestingly, one of the pentatricopeptide repeat (PPR) gene family members, MpPPR_66 (LW9825), the protein products of which are generally involved in various steps of RNA metabolism, has a long stem-loop transcript that can generate Mpo-miR11692.1 to autoregulate MpPPR_66 (LW9825) mRNA. This study provides a foundation for further investigations of the RNA-mediated silencing mechanism in M. polymorpha as well as of the evolution of this gene silencing pathway in embryophytes.

摘要

苔藓植物(叶苔、角苔和藓类)包含陆地植物(有胚植物)最早分化出的三个谱系。多形叶苔是一种复杂的叶状体叶苔纲叶苔,已发展成为一个模式遗传系统,占据关键的系统发育位置。因此,多形叶苔在旨在阐明植物基因调控机制进化的研究中很有用。在本研究中,我们使用计算、转录组、小RNA和降解组分析来表征多形叶苔中微小RNA(miRNA)介导的基因调控途径。这些数据已整合到开放获取的ContigViews-miRNA平台以供进一步参考。除了miRNA途径的核心成分外,还鉴定出129个独特的miRNA序列,其中11个可归类为在有胚植物中保守的7个miRNA家族(miR166a、miR390、miR529c、miR171-3p、miR408a、miR160和miR319a)。计算分析和降解组分析相结合使我们能够鉴定并通过实验验证249个靶标。在某些情况下,靶基因与其他有胚植物的靶基因是直系同源的,但在其他情况下,保守的miRNA靶向旁系同源物或不同基因家族的成员。此外,新发现的Mpo-miR11707.1和Mpo-miR11707.2由一个共同前体产生,并靶向MpARGONAUTE1(LW1759)。另外两个新发现的miRNA,Mpo-miR11687.1和Mpo-miR11681.1,分别靶向MADS盒转录因子MpMADS1和MpMADS2。有趣的是,五肽重复(PPR)基因家族成员之一MpPPR_66(LW9825),其蛋白质产物通常参与RNA代谢的各个步骤,有一个长茎环转录本,可产生Mpo-miR11692.1以自我调节MpPPR_66(LW9825)的mRNA。本研究为进一步研究多形叶苔中RNA介导的沉默机制以及该基因沉默途径在有胚植物中的进化提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b321/4788410/8467e4b7f3e3/pcw020f1p.jpg

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