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Next-generation sequencing of the Chinese hamster ovary microRNA transcriptome: Identification annotation and profiling of microRNAs as targets for cellular engineering

机译:中国仓鼠卵巢microRNA转录组的下一代测序:作为细胞工程靶标的microRNA的鉴定注释和分析

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摘要

Chinese hamster ovary (CHO) cells are the predominant cell factory for the production of recombinant therapeutic proteins. Nevertheless, the lack in publicly available sequence information is severely limiting advances in CHO cell biology, including the exploration of microRNAs (miRNA) as tools for CHO cell characterization and engineering. In an effort to identify and annotate both conserved and novel CHO miRNAs in the absence of a Chinese hamster genome, we deep-sequenced small RNA fractions of 6 biotechnologically relevant cell lines and mapped the resulting reads to an artificial reference sequence consisting of all known miRNA hairpins. Read alignment patterns and read count ratios of 5′ and 3′ mature miRNAs were obtained and used for an independent classification into miR/miR* and 5p/3p miRNA pairs and discrimination of miRNAs from other non-coding RNAs, resulting in the annotation of 387 mature CHO miRNAs. The quantitative content of next-generation sequencing data was analyzed and confirmed using qPCR, to find that miRNAs are markers of cell status. Finally, cDNA sequencing of 26 validated targets of miR-17-92 suggests conserved functions for miRNAs in CHO cells, which together with the now publicly available sequence information sets the stage for developing novel RNAi tools for CHO cell engineering.
机译:中国仓鼠卵巢(CHO)细胞是生产重组治疗性蛋白质的主要细胞工厂。尽管如此,缺乏公开可用的序列信息严重限制了CHO细胞生物学的进展,包括对microRNA(miRNA)的探索作为CHO细胞表征和工程化的工具。为了在没有中国仓鼠基因组的情况下鉴定和注释保守的和新颖的CHO miRNA,我们对6种与生物技术相关的细胞系的小RNA片段进行了深度测序,并将得到的读数映射到由所有已知miRNA组成的人工参考序列上发夹。获得了5'和3'成熟miRNA的阅读比对模式和阅读计数比,并将其用于miR / miR *和5p / 3p miRNA对的独立分类以及miRNA与其他非编码RNA的区分,从而注释了387个成熟的CHO miRNA。使用qPCR分析和确认了下一代测序数据的定量内容,以发现miRNA是细胞状态的标志。最后,对miR-17-92的26个经过验证的靶标进行cDNA测序表明,CHO细胞中miRNA的保守功能与目前公开的序列信息一起为开发用于CHO细胞工程的新型RNAi工具奠定了基础。

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