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深入未知:利用下一代测序技术在 CHO 中进行无基因组序列信息的表达谱分析。

Into the unknown: expression profiling without genome sequence information in CHO by next generation sequencing.

机构信息

Department of Pulmonary Research, Group Genomics, Boehringer Ingelheim Pharma GmbH & Co KG, Birkendorferstrasse 67, 88397 Biberach an der Riss, Germany.

出版信息

Nucleic Acids Res. 2010 Jul;38(12):3999-4010. doi: 10.1093/nar/gkq116. Epub 2010 Mar 1.

DOI:10.1093/nar/gkq116
PMID:20194116
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2896516/
Abstract

The arrival of next-generation sequencing (NGS) technologies has led to novel opportunities for expression profiling and genome analysis by utilizing vast amounts of short read sequence data. Here, we demonstrate that expression profiling in organisms lacking any genome or transcriptome sequence information is feasible by combining Illumina's mRNA-seq technology with a novel bioinformatics pipeline that integrates assembled and annotated Chinese hamster ovary (CHO) sequences with information derived from related organisms. We applied this pipeline to the analysis of CHO cells which were chosen as a model system owing to its relevance in the production of therapeutic proteins. Specifically, we analysed CHO cells undergoing butyrate treatment which is known to affect cell cycle regulation and to increase the specific productivity of recombinant proteins. By this means, we identified sequences for >13,000 CHO genes which added sequence information of approximately 5000 novel genes to the CHO model. More than 6000 transcript sequences are predicted to be complete, as they covered >95% of the corresponding mouse orthologs. Detailed analysis of selected biological functions such as DNA replication and cell cycle control, demonstrated the potential of NGS expression profiling in organisms without extended genome sequence to improve both data quantity and quality.

摘要

下一代测序 (NGS) 技术的出现为表达谱分析和基因组分析提供了新的机会,利用大量的短读序列数据。在这里,我们通过将 Illumina 的 mRNA-seq 技术与一个新的生物信息学管道相结合,展示了在缺乏任何基因组或转录组序列信息的生物体中进行表达谱分析是可行的,该管道整合了组装和注释的中国仓鼠卵巢 (CHO) 序列以及来自相关生物体的信息。我们将该管道应用于 CHO 细胞的分析,CHO 细胞被选为模型系统,因为它与治疗性蛋白质的生产有关。具体来说,我们分析了正在经历丁酸盐处理的 CHO 细胞,丁酸盐处理已知会影响细胞周期调控并提高重组蛋白的特异性产率。通过这种方法,我们鉴定了超过 13000 个 CHO 基因的序列,为 CHO 模型增加了大约 5000 个新基因的序列信息。超过 6000 个转录本序列被预测为完整的,因为它们覆盖了相应的小鼠同源物的 >95%。对 DNA 复制和细胞周期控制等选定生物学功能的详细分析表明,在没有扩展基因组序列的生物体中进行 NGS 表达谱分析具有提高数据数量和质量的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/38aa4f22dacd/gkq116f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/e4116a1a583b/gkq116f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/faf0a9b25d67/gkq116f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/54805238bac6/gkq116f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/5d39444b6752/gkq116f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/38aa4f22dacd/gkq116f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/e4116a1a583b/gkq116f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/faf0a9b25d67/gkq116f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/54805238bac6/gkq116f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/5d39444b6752/gkq116f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c652/2896516/38aa4f22dacd/gkq116f5.jpg

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