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EST sequencing and gene expression profiling in Scutellaria baicalensis

机译:黄ical的EST测序及基因表达谱分析

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摘要

Scutellaria baicalensis is an important medicinal plant, but few genomic resources are available for this species, as well as for other non-model plants. One of the major new directions in genome research is to discover the full spectrum of genes transcribed from the whole genome. Here, we report extensive transcriptome data of the early growth stage of S. baicalensis. This transcriptome consensus sequence was constructed by de novo assembly of shotgun sequencing data, obtained using multiple next-generation DNA sequencing (NGS) platforms (Roche/454 GS_FLX+ and Illumina/Solexa HiSeq2000). We show that this new approach to obtain extensive mRNA is an efficient strategy for genome-wide transcriptome analysis. We obtained 1,226,938 and 161,417,646 reads using the GS_FLX and the Illumina/Solexa HiSeq2000, respectively. De novo assembly of the high-quality GS_FLX and Illumina reads (95 % and 75 %) resulted in more than 82 Mb of mRNA consensus sequence, which we assembled into 51,188 contigs, with at least 500 bp per contig. Of these contigs, 39,581 contained known genes, as determined by BLASTX searches against non-redundant NCBI database. Of these, 20,498 different genes were expressed during the early growth stage of S. baicalensis. We have made the expressed sequences available on a public database. Our results demonstrate the utility of combining NGS technologies as a basis for the development of genomic tools in non-model, medicinal plant species. Knowledge of all described genes and quantitation of the expressed genes, including the transcription factors involved, will be useful in studies of the biology of S. baicalensis gene regulation.
机译:黄cut是重要的药用植物,但该物种以及其他非典范植物的基因组资源很少。基因组研究的主要新方向之一是发现从整个基因组转录的全部基因。在这里,我们报告广泛的转录组数据,黄ba的早期生长阶段。该转录组共有序列是通过shot弹枪测序数据的从头组装而构建的,该序列是使用多个下一代DNA测序(NGS)平台(Roche / 454 GS_FLX +和Illumina / Solexa HiSeq2000)获得的。我们表明,这种获得广泛的mRNA的新方法是全基因组转录组分析的有效策略。我们分别使用GS_FLX和Illumina / Solexa HiSeq2000获得了1,226,938和161,417,646读数。从头开始组装高质量的GS_FLX和Illumina读物(分别为95%和75%),产生了超过82 Mb的mRNA共有序列,我们将其组装成51188个重叠群,每个重叠群至少500 bp。这些重叠群中,有39,581个包含已知基因,这是通过BLASTX搜索非冗余NCBI数据库确定的。其中,在黄ical的早期生长阶段表达了20,498种不同的基因。我们已经在公共数据库中提供了表达的序列。我们的结果证明了结合NGS技术作为开发非模型药用植物物种中的基因组工具的基础的实用性。了解所有描述的基因和表达的基因(包括涉及的转录因子)的定量,将有助于黄ba链球菌基因调控的生物学研究。

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