Biotherapeutics Translational Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon, South Korea; Department of Bioprocess Engineering, KRIBB School of Biotechnology, Korea University of Science and Technology (UST), 217 Gajeong-ro, Yuseong-gu, Daejeon, South Korea.
Biotherapeutics Translational Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon, South Korea; Department of Biological Sciences, KAIST, 335 Gwahak-ro, Yuseong-gu, Daejeon, South Korea.
J Biotechnol. 2018 Oct 10;283:37-42. doi: 10.1016/j.jbiotec.2018.07.018. Epub 2018 Jul 18.
Sodium butyrate (NaBu) is an efficient supplement for increasing recombinant protein production in Chinese hamster ovary (CHO) cell culture. To elucidate the effects of NaBu on miRNA expression profile in recombinant CHO (rCHO) cells, differentially expressed miRNAs in NaBu-treated rCHO cells were assessed by NanoString nCounter analysis. This result showed that eight mature mouse miRNAs (let-7b, let-7d, miR-15b, miR-25, miR-27a, miR-99a, miR-125a-5p, and miR-125b-5p) were differentially expressed. Furthermore, quantitative real-time RT-PCR analysis of eight mature CHO miRNAs, annotated using a miRBase database, confirmed the transcriptomic findings. Among the potential corresponding target mRNAs for the selected mature miRNAs, seven cell growth-related target genes (e2f2, akt2, mtor, bcl-2, bim, p38α, and bmf) and five N-glycosylation-related target genes (neu1, b4galt3, gale, man1b1 and mgat4a) were selected by considering the effectiveness of NaBu on rCHO cell culture. The altered expression patterns of the 12 target mRNAs were inversely correlated with those of the selected mature miRNAs. Altogether, NanoString nCounter analysis may be useful for identifying differentially expressed miRNAs in rCHO cells.
丁酸钠(NaBu)是一种有效的补充剂,可提高中国仓鼠卵巢(CHO)细胞培养中重组蛋白的产量。为了阐明 NaBu 对重组 CHO(rCHO)细胞中 miRNA 表达谱的影响,通过 NanoString nCounter 分析评估了 NaBu 处理的 rCHO 细胞中差异表达的 miRNA。结果表明,有 8 个成熟的小鼠 miRNA(let-7b、let-7d、miR-15b、miR-25、miR-27a、miR-99a、miR-125a-5p 和 miR-125b-5p)差异表达。此外,使用 miRBase 数据库注释的 8 个成熟 CHO miRNA 的定量实时 RT-PCR 分析证实了转录组发现。在选择的成熟 miRNA 的潜在相应靶 mRNA 中,考虑到 NaBu 对 rCHO 细胞培养的有效性,选择了 7 个与细胞生长相关的靶基因(e2f2、akt2、mtor、bcl-2、bim、p38α 和 bmf)和 5 个与 N-糖基化相关的靶基因(neu1、b4galt3、gale、man1b1 和 mgat4a)。12 个靶 mRNA 的表达模式改变与所选成熟 miRNA 的表达模式呈负相关。总之,NanoString nCounter 分析可能有助于鉴定 rCHO 细胞中差异表达的 miRNA。