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Volume 32 Issue 2
Apr.  2017
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Article Contents
GAO Xiang-feng, WANG Rang-jian, LIU Feng-jing, LI Hui-ling. Hydroponic Culturein Sample Preparation of Tea Shoots for RNA Sequencing[J]. Fujian Journal of Agricultural Sciences, 2017, 32(2): 155-160. doi: 10.19303/j.issn.1008-0384.2017.02.010
Citation: GAO Xiang-feng, WANG Rang-jian, LIU Feng-jing, LI Hui-ling. Hydroponic Culturein Sample Preparation of Tea Shoots for RNA Sequencing[J]. Fujian Journal of Agricultural Sciences, 2017, 32(2): 155-160. doi: 10.19303/j.issn.1008-0384.2017.02.010

Hydroponic Culturein Sample Preparation of Tea Shoots for RNA Sequencing

doi: 10.19303/j.issn.1008-0384.2017.02.010
  • Received Date: 2016-08-25
  • Rev Recd Date: 2016-11-18
  • Publish Date: 2017-02-01
  • Valid sampling is essential to obtain reliable transcripts of genetic information for biological studies. For RNA sequencing, the integrity, purity and concentration of total RNA as well as the cDNA libraries and transcriptome sequencingon two specimens of tea shoots sampled by using two methods were compared. One of the methods was hydroponic culture (SM1), and another, dry ice freezing (SM2). The results showed that both of them yielded RNA extractions with high integrity and purity without significant differences on the measured concentrations. They were well satisfied for the subsequent transcriptome sequencing, also capable of obtaining the equivalent cDNA libraries and RNA sequencing. However, SM1 was simpler and more convenient than SM2 in handling and operation, and particularly suitable for field sampling. Aside from being used on tea, SM1 could be applied on other crops in preparing samples for extracting RNA as well.
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  • [1]
    SHEEJA T E, DEEPA K, SANTHI R, et al. Comparative Transcriptome Analysis of Two Species of Curcuma Contrasting in a High-Value Compound Curcumin: Insights into Genetic Basis and Regulation of Biosynthesis[J]. Plant Mol Biol Rep, 2015, 33: 1825-1836. doi: 10.1007/s11105-015-0878-6
    [2]
    QIANG ZHOU, DONG LUO, LICHAO MA, et al. Development and cross-species transferability of EST-SSR markers in Siberian wildrye (Elymus sibiricus L.) using Illumina sequencing[J]. Scientific Reports, 2016, 6: 20549. doi: 10.1038/srep20549
    [3]
    XIAOHUI ZHANG, TONGJIN LIU, MENGMENG DUAN, et al. De novo Transcriptome Analysis of Sinapis alba in Revealing the Glucosinolate and Phytochelatin Pathways[J].Frontiers in Plant Science, 2016, 7: 259. https://www.researchgate.net/publication/297604244_De_novo_Transcriptome_Analysis_of_Sinapis_alba_in_Revealing_the_Glucosinolate_and_Phytochelatin_Pathways
    [4]
    DAN WANG, CHUN-FANG LI, CHUN-LEI MA, et al. Novel insights into the molecular mechanisms underlying the resistance of Camellia sinensis to Ectropis oblique provided by strategic transcriptomic comparisons[J]. Scientia Horticulturae, 2015, 192: 429-440. doi: 10.1016/j.scienta.2015.06.005
    [5]
    CHUN-FANG LI, YAN ZHU, YAO YU, et al. Global transcriptome and gene regulation network for secondary metabolite biosynthesis of tea plant (Camellia sinensis)[J]. BMC Genomics, 2015, 16: 560. doi: 10.1186/s12864-015-1773-0
    [6]
    QUANJIN WU, ZHIDAN CHEN, WEIJIANG SUN, et al. De novo Sequencing of the Leaf Transcriptome Reveals Complex Light-Responsive Regulatory Networks in Camellia sinensis cv.Baijiguan[J]. Frontiers in Plant Science, 2016, 7: 332. http://www.pubfacts.com/detail/27047513/De-novo-Sequencing-of-the-Leaf-Transcriptome-Reveals-Complex-Light-Responsive-Regulatory-Networks-in
    [7]
    宛晓春, 夏涛.茶树次生代谢[M].北京:科学出版社, 2015.
    [8]
    SCHNEIDERBAUER A, SANDERMANN H J, ERNST D. Isolation of functional RNA from plant tissues rich in phenolic compounds[J]. Anal Biochem, 1991, 197: 91-95. doi: 10.1016/0003-2697(91)90360-6
    [9]
    WANG C S, VODKIN L O. Extraction of RNA from tissues containing high levels of procyanidins that bind RNA[J]. Plant Mol Biol Rep, 1994, 12: 132-145. doi: 10.1007/BF02668374
    [10]
    LEWINSOHN E, STEELE C L, CROTEAU R. Simple isolation of functional RNA from woody stems of gym nosperms[J]. Plant Mol Biol Rep, 1994, 12: 20-25. doi: 10.1007/BF02668660
    [11]
    GRAHAM G C. A method for extraction of total RNA from Pinus radiata and other conifers[J]. Plant Mol Biol Rept, 1993, 11:32-37. doi: 10.1007/BF02670557
    [12]
    江昌俊, 王朝霞, 李叶云.茶树中提纯总RNA的研究[J].茶叶科学, 2000, 20(1): 27-29. http://www.cnki.com.cn/Article/CJFDTOTAL-CYKK200001005.htm
    [13]
    林金科, 开国银.茶树RNA的提纯与鉴定[J].福建农林大学学报:自然科学版, 2003, 32(1): 70-73. http://www.cnki.com.cn/Article/CJFDTOTAL-FJND200301017.htm
    [14]
    史成颖, 宛晓春, 江昌俊, 等.提取高质量茶树总RNA的方法研究[J].安徽农业大学学报, 2007, 34(3): 360-363. http://www.cnki.com.cn/Article/CJFDTOTAL-ANHU200703012.htm
    [15]
    杨冬青, 王云生, 孙美莲, 等.茶树不同器官组织总RNA提取方法的研究[J].激光生物学报, 2011, 20(1): 108-115. http://www.cnki.com.cn/Article/CJFDTOTAL-JGSW201101023.htm
    [16]
    GRABHERR M G, HAAS B J, YASSOUR M, et al. Full-length transcriptome assembly from RNA-Seq data without a reference genome[J]. Nat Biotechnol, 2011, 29: 644-652. doi: 10.1038/nbt.1883
    [17]
    LI B, DEWEY C N.RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome[J]. BMC Bioinf, 2011, 12: 323. doi: 10.1186/1471-2105-12-323
    [18]
    林德光.析因试验中交互作用分析的SAS技术[J].工科数学, 2001, 17(4):48-54. http://www.cnki.com.cn/Article/CJFDTOTAL-GKSX200104012.htm
    [19]
    王镜岩, 朱圣庚, 徐长发.生物化学:第三版[M].北京:高等教育出版社, 2002.
    [20]
    ZHANG J D, SCHINDLER T, KUNG E, et al. Highly sensitive amplicon-based transcript quantification by semiconductor sequencing[J]. BMC Genomics, 2014, 15: 565. doi: 10.1186/1471-2164-15-565
    [21]
    WANG Z, GERSTEIN M, SNYDER M. RNA-Seq: a revolutionary tool for transcriptomics[J]. Nat Rev Genet, 2009, 10: 57-63. doi: 10.1038/nrg2484
    [22]
    李宏, 王新力.植物组织RNA提取的难点及对策[J].生物技术通报, 1999, (1):36-39. http://www.cnki.com.cn/Article/CJFDTOTAL-SWJT901.008.htm
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