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转录组研究新技术:RNA-Seq及其应用 被引量:203

RNA-Seq and its applications:a new technology for transcriptomics
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摘要 转录组是特定组织或细胞在某一发育阶段或功能状态下转录出来的所有RNA的集合。转录组研究能够从整体水平研究基因功能以及基因结构,揭示特定生物学过程以及疾病发生过程中的分子机理。RNA-Seq作为一种新的高效、快捷的转录组研究手段正在改变着人们对转录组的认识。RNA-Seq利用高通量测序技术对组织或细胞中所有RNA反转录而成的cDNA文库进行测序,通过统计相关读段(reads)数计算出不同RNA的表达量,发现新的转录本;如果有基因组参考序列,可以把转录本映射回基因组,确定转录本位置、剪切情况等更为全面的遗传信息,已广泛应用于生物学研究、医学研究、临床研究和药物研发等。文章主要介绍了RNA-Seq原理、技术特点及其应用,并就RNA-Seq技术面临的挑战和未来发展前景进行了讨论,为今后该技术的研究与应用提供参考。 The transcriptome is the complete set of transcripts for certain type of cells or tissues in a specific developmental stage or physiological condition.Transcriptome analysis can provide a comprehensive understanding of molecular mechanisms involved in specific biological processes and diseases from the information on gene structure and function.Transcriptome has been challenging due to the efficient and fast procedures of RNA-seq.RNA-seq,refers to the use of high-throughput sequencing technologies to sequence cDNA library transcribed from all RNAs in tissues or cells,can be used to quantify,profile,and discover RNA transcripts by sequence reads.Thus,the transcripts can then be mapped on the reference genome to get comprehensive genetic information,such as transcription localization and alternative splicing status.RNA-Seq has been widely used in biological,medical,clinical and pharmaceutical research.The detailed principles,technical characteristics and applications of RNA-seq are reviewed here,and the challenges and application potentials of RNA-seq in the future are also discussed.This will present the useful information for other researchers.
出处 《遗传》 CAS CSCD 北大核心 2011年第11期1191-1202,共12页 Hereditas(Beijing)
基金 内蒙古自然科学基金项目(编号:2010BS0405) 国家现代肉羊产业技术体系(编号:nycytx-39)资助
关键词 RNA-SEQ 转录组 新一代测序技术 RNA-Seq transcriptome next-generation sequencing(NGS) technology
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  • 1Croucher N J, Fookes MC, Perkins TT, Turner D J, Mar- guerat SB, Keane T, Quail MA, He M, Assefa S, B~ihler J, Kingsley RA, Parkhill J, Bentley SD, Dougan G, Thomson NR. A simple method for directional transcriptome se- quencing using Illumina technology. Nucleic Acids Res, 2009, 37(22): e148.
  • 2Shendure J, Ji H. Next-generation DNA sequencing. Nat Biotechnol, 2008, 26(10): 1135-1145.
  • 3Vliet VA. Next generation sequencing of microbial tran- scriptomes: challenges and opportunities. FEMS Microbiol Lett, 2010, 302(1): 1-7.
  • 4Margulies M, Egholm M, Altman WE, Attiya S, Bader JS, Bemben LA, Berka J, Braverman MS, Chen YJ, Chen ZT, Dewell SB, Du L, Fierro JM, Gomes XV, Godwin BC, He W, Helgesen S, Ho CH, Irzyk GP, Jando SC, Alenquer ML, Jarvie TP, Jirage KB, Kim JB, Knight JR, Lanza JR, Lea- mon JH, Lefkowitz SM, Lei M, Li J, Lohman KL, Lu H, Makhijani VB, McDade KE, McKenna MP, Myers EW, Nickerson E, Nobile JR, Plant R, Puc BP, Ronan MT, Roth GT, Sarkis GJ, Simons JF, Simpson JW, Srinivasan M, Tartaro KR, Tomasz A, Vogt KA, Volkmer GA, Wang SH, Wang Y, Weiner MP, Yu PG, Begley RF, Rothberg JM. Genome sequencing in microfabricated high-density pico- litre reactors. Nature, 2005, 437(7057): 376-380.
  • 5Lockhart D J, Winzeler EA. Genomics, gene expression and DNA arrays. Nature, 2000, 405(6788): 827-836.
  • 6Ozsolak F, Milos PM. RNA sequencing: advances, chal- lenges and opportunities. Nat Rev Genet, 2011, 12(2): 87-98.
  • 7Vivancos AP, Gtiell M, Dohm JC, Serrano L, Himmel- bauer H. Strand-specific deep sequencing of the tran- scriptome. Genome Res, 2010, 20(7): 989-999.
  • 8Wilhelm BT, Marguerat S, Watt S, Schubert F, Wood V,Goodhead I, Penkett C J, JaneRogers J, B~ihler J. Dynamic repertoire of a eukaryotic transcriptome surveyed at sin- gle-nucleotide resolution. Nature, 2008, 453(7199): 1239- 1243.
  • 9Yao YY, Guo GG, Ni ZF, Sunkar R, Du JK, Zhu JK, Sun QX. Cloning and characterization of microRNAs from wheat (Triticum aestivum L.). Genome Biol, 2007, 8(6): R96.
  • 10Tang FC, Barbacioru C, Wang YZ, Nordman E, Lee C, Xu NL, Wang XH, Bodeau J, Tuch BB, Siddiqui A, Lao KQ, Surani MA. mRNA-Seq whole-transcriptome analysis of a single cell. Nat Methods, 2009, 6(5): 377-382.

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