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Robust analysis of 5'-transcript ends (5'-RATE): a novel technique for transcriptome analysis and genome annotation

机译:5'-转录物末端的稳健分析(5'-RATE):转录组分析和基因组注释的新技术

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Complicated cloning procedures and the high cost of sequencing have inhibited the wide application of serial analysis of gene expression and massively parallel signature sequencing for genome-wide transcriptome profiling of complex genomes. Here we describe a new method called robust analysis of 5'-transcript ends (5'-RATE) for rapid and cost-effective isolation of long 5' transcript ends (80 bp). It consists of three major steps including 5'-oligocapping of mRNA, NlaIII tag and ditag generation, andpyrosequencing of NlaIII tags. Complicated steps, such as purification and cloning of concatemers, colony picking and plasmid DNA purification, are eliminated and the conventional Sanger sequencing method is replaced with the newly developed pyrosequencing method. Sequence analysis of a maize 5'-RATE library revealed complex alternative transcription start sites and a 5' poly(A) tail in maize transcripts. Our results demonstrate that 5'-RATE is a simple, fast and cost-effective method for transcriptome analysis and genome annotation of complex genomes.
机译:复杂的克隆程序和高昂的测序成本,阻碍了基因表达的串行分析和复杂基因组范围内全基因组转录组分析的大规模平行签名测序的广泛应用。在这里,我们描述了一种新的方法,称为5'-转录物末端的稳健分析(5'-RATE),可快速且经济高效地分离长的5'-转录物末端(80 bp)。它包括三个主要步骤,包括mRNA的5'-寡聚,NlaIII标签和双标签生成以及NlaIII标签的焦磷酸测序。消除了复杂的步骤,例如连接体的纯化和克隆,菌落的挑选以及质粒DNA的纯化,并且用新开发的焦磷酸测序方法代替了传统的Sanger测序方法。玉米5'-RATE文库的序列分析揭示了玉米转录物中复杂的替代转录起始位点和5'poly(A)尾巴。我们的结果表明5'-RATE是一种简单,快速且经济高效的方法,用于复杂基因组的转录组分析和基因组注释。

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