研究报告

蒙古沙冬青保守microRNAs的鉴定及靶基因预测

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  • 中央民族大学生命与环境科学学院, 北京 100081
高飞, 博士, 副教授, 研究方向:植物逆境分子生物学。Tel: 010-68932633; E-mail: gaofei@muc.edu.cn

收稿日期: 2013-10-23

  修回日期: 2014-01-07

  网络出版日期: 2014-05-25

基金资助

国家自然科学基金项目(编号:31070361, 31370356), 教育部科学技术研究重点项目(编号:210266)和国家985工程项目和高等学校学科创新引智计划项目(编号:B08044)资助

Identification and target prediction of conserved microRNAs in Ammopiptanthus mongolicus

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  • College of Life and Environmental Sciences, Minzu University of China, Beijing 100081, China

Received date: 2013-10-23

  Revised date: 2014-01-07

  Online published: 2014-05-25

摘要

蒙古沙冬青(Ammopiptanthus mongolicus)是生长在荒漠中的木本植物, 对于我国西北部干旱、半干旱区域的植被维护与恢复具有重要价值。蒙古沙冬青对干旱、低温等多种逆境具有较高的耐受性, 是研究林木耐受逆境生理与分子机制的合适材料。MicroRNA(miRNA)是一类长度约为21个核苷酸的内源性非编码小分子RNA, 在植物生长发育和逆境应答等生物学过程中发挥着重要的调控作用。目前, 许多植物物种的miRNAs已经获得鉴定, 但未见蒙古沙冬青miRNAs的相关报道。文章应用高通量测序和生物信息学分析方法对蒙古沙冬青幼苗保守miRNAs的类型、表达丰度以及靶基因进行了分析和预测。共鉴定了10个家族的19种保守miRNAs, 其表达丰度介于55~1920269个拷贝之间。通过在线软件psRNATarget预测了其中14个保守miRNAs的靶基因。对于这些靶基因的功能分析表明, 蒙古沙冬青的保守miRNA主要通过转录调控、激素信号途径、物质代谢和胁迫应答等生物学过程参与植物生长发育和环境响应。

本文引用格式

高飞, 孙鹏, 陈静, 李章磊, 张孜宸, 李华云, 王宁, 周宜君 . 蒙古沙冬青保守microRNAs的鉴定及靶基因预测[J]. 遗传, 2014 , 36(5) : 485 -494 . DOI: 10.3724/SP.J.1005.2014.0485

Abstract

Ammopiptanthus mongolicus, a woody plant growing in the desert, plays a vital role in vegetation maintaining and restoration in the arid region in northwest China. The plant exhibits an extremely high tolerance to abiotic stress such as drought and freezing stresses, and it has been used as an ideal model for abiotic stress tolerance research in trees. Mi-croRNA (miRNA) is a class of approximately 21nt endogenous non-protein-coding small RNA, which plays an important role in plant growth, development and responses to environmental stresses. By now, a large number of miRNAs have been reported in many plant species, but no studies describing A.mongolicus miRNA were published. In the present study, the types, expression levels, and putative target genes of conserved miRNAs in seedlings of A. mongolicus were analyzed using small RNA deep sequencing technology and bioinformatics methods. Nineteen conserved miRNAs, which belong to 10 miRNA families, were identified, with abundance ranging from 55 to 1920269 reads. Target prediction analysis determined the target genes of 14 conserved miRNAs. The functional classification analysis indicated that the conserved miRNAs par-ticipate in the development and environmental response by regulating the biological processes including the transcription regulation, hormone signal transduction, metabolisms and stress resistance.

参考文献

[1] Carrington JC, Ambros V. Role of microRNAs in plant and animal development. Science, 2003, 301(5631): 336–338. <\p>

[2] Ambros V, Bartel B, Bartel DP, Burge CB, Carrington JC, Chen X, Dreyfuss G, Eddy SR, Griffiths-Jones S, Marshall M, Matzke M, Ruvkun G, Tuschl T. A uniform system for microRNA annotation. RNA, 2003, 9(3): 277–279. <\p>

[3] Meyers BC, Axtell MJ, Bartel B, Bartel DP, Baulcombe D, Bowman JL, Cao X, Carrington JC, Chen X, Green PJ, Griffiths-Jones S, Jacobsen SE, Mallory AC, Martienssen RA, Poethig RS, Qi Y, Vaucheret H, Voinnet O, Watanabe Y, Weigel D, Zhu JK. Criteria for annotation of plant Mi-croRNAs. Plant Cell, 2008, 20(12): 3186–3190. <\p>

[4] Kozomara A, Griffiths-Jones S. miRBase: integrating mi-croRNA annotation and deep-sequencing data. Nucleic Acids Res, 2011, 39(Database issue): D152–D157. <\p>

[5] Zuker M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res, 2003, 31(13): 3406–3415. <\p>

[6] Dai X, Zhao PX. psRNATarget: a plant small RNA target analysis server. Nucleic Acids Res, 2011, 39(Web Server issue): W155–W159. <\p>

[7] Llave C, Kasschau KD, Rector MA, Carrington JC. En-dogenous and silencing-associated small RNAs in plants. Plant Cell, 2002, 14(7): 1605–1619. <\p>

[8] Griffiths-Jones S, Saini HK, van Dongen S, Enright AJ. miRBase: tools for microRNA genomics. Nucleic Acids Res, 2008, 36(Database Issue): D154–D158. <\p>

[9] Ge XJ, Yu Y, Yuan YM, Huang HW, Yan C. Genetic diver-sity and geographic differentiation in endangered Ammopiptanthus (Leguminosae) populations in desert regions of northwest China as revealed by ISSR analysis. Ann Bot, 2005, 95(5): 843–851. <\p>

[10] 林清芳, 王茅雁, 刘佳杰, 赵欢欢, 王存芳. 沙冬青细胞与分子生物学研究进展. 植物遗传资源学报, 2010, 11(6): 793–797. <\p>

[11] Liu JQ, Qiu MX. Ecological, physiological and anatomical traits of Ammopiptanthus mongolicus grown in desert of China. Acta Bot Sin, 1982, 24(6): 568–573. <\p>

[12] Lu CF, Yin LK, Li KH. Proteome expression patterns in the stress tolerant evergreen Ammopiptanthus nanus under conditions of extreme cold. Plant Growth Regul, 2010, 62(1): 65–70. <\p>

[13] Wei Q, Guo YJ, Cao HM, Kuai BK. Cloning and charac-terization of anAtNHX2-like Na+/H+antiporter gene from Ammopiptanthusmongolicus(Leguminosae) and its ectopic expression enhanced drought and salt tolerance in Arabidopsis thaliana. Plant Cell Tiss Organ Cult, 2011, 105(3): 309–316. <\p>

[14] Liu RL, Liu MQ, Liu J, Chen YZ, Chen YY, Lu CF. Het-erologous expression of a Ammopiptanthus mongolicus late embryogenesis abundant protein gene (AmLEA) en-hances Escherichia coli viability under cold and heat stress. Plant Growth Regul, 2010, 60(2): 163–168. <\p>

[15] Chen JH, Sun Y, Sun F, Xia XL, Yin WL. Tobacco plants ectopically expressing the Ammopiptanthus mongolicus AmCBL1gene display enhanced tolerance to multiple abiotic stresses. Plant Growth Regul, 2011, 63(3): 259–269. <\p>

[16] Zhou Y, Gao F, Liu R, Feng J, Li H. De novo sequencing and analysis of root transcriptome using 454 pyrosequencing to discover putative genes associated with drought tolerance in Ammopiptanthusmongolicus. BMC Genomics, 2012, 13: 266. <\p>

[17] Pang T, Ye CY, Xia X, Yin W. De novo sequencing and transcript me analysis of the desert shrub, Ammopiptanthus mongolicus, during cold acclimation using Illumina/ Solexa. BMC Genomics, 2013, 14(1): 488. <\p>

[18] Zhao CZ, Xia H, Frazier TP, Yao YY, Bi YP, Li AQ, Li MJ, Li CS, Zhang BH, Wang XJ. Deep sequencing identifies novel and conserved microRNAs in peanuts (Arachis hy-pogaea L.). BMC Plant Biol, 2010, 10: 3. <\p>

[19] Krishna S, Nair A, Cheedipudi S, Poduval D, Dhawan J, Palakodeti D, Ghanekar Y. D

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