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Automated transition analysis of activated gene regulation during diauxicnutrient shift in Escherichia coli and adipocyte differentiation in mouse cells

机译:大肠杆菌和脂肪细胞分化中的辅助营养因子在小鼠细胞中的激活基因调控的自动转变分析

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Background: Comprehensively understanding the dynamics of biological systems is among the biggest current challenges in biology and medicine. To acquire this understanding, researchers have measured the time-series expression profiles of cell lines of various organisms. Biological technologies have also drastically improved, providing a huge amount of information with support from bioinformatics and systems biology. However, the transitions between the activation and inactivation of gene regulations, atthe temporal resolution of single time points, are difficult to extract from time-course gene expression profiles.Results: Our proposed method reports the activation period of each gene regulation from gene expression profiles and a gene regulatory network. The correctness and effectiveness of the method were validated by analyzing the diauxic shift from glucose tolactose in Escherichia coli. The method completely detected the three periods of the shift; 1) consumption of glucose as nutrient source, 2) the period of seeking another nutrient source and 3) consumption of lactose as nutrient source. We then applied the method to mouse adipocyte differentiation data. Cell differentiation into adipocytes is known to involve two waves of the gene regulation cascade, and sub-waves are predicted. From the gene expression profiles of the cell differentiation process fromES to adipose cells (62 time points), our method acquired four periods; three periods covering the two known waves of the cascade, and a final period of gene regulations when the differentiation to adipocytes was completed.Conclusions: Our proposed method identifies the transitions of gene regulations from time-series gene expression profiles. Dynamic analyses are essential for deep understanding of biological systems and for identifying the causes of the onset of diseasessuch as diabetes and osteoporosis. The proposed method can greatly contribute to the progress of biology and medicine.
机译:背景:全面理解生物系统的动态是生物学和医学中最大的当前挑战之一。为了获得这种理解,研究人员已经测量了各种生物的细胞系的时间序列表达谱。生物技术也彻底改善,提供了大量信息,支持生物信息学和系统生物学。然而,在单时间点的时间分辨率的基因规则的激活和失活之间的转变难以从时机基因表达谱中提取。结果:我们的提出方法报告了来自基因表达谱的每个基因调控的激活时间和基因监管网络。通过分析来自大肠杆菌中的葡萄糖耐溶乳糖的辅助偏移来验证该方法的正确性和有效性。该方法完全检测到班次的三个时期; 1)葡萄糖的消耗作为营养源,2)寻求另一种营养素来源的时期和3)乳糖消耗作为营养源。然后,我们将该方法应用于鼠标adipocyte差异化数据。已知细胞分化成脂肪细胞涉及基因调节级联的两波,并且预测子波。从细胞分化过程的基因表达谱到脂肪细胞(62个时间点),我们的方法获得了四个时期;覆盖级联的两个已知波的三个时期,以及当完成与脂肪细胞的分化时的基因规则的最后一段时间。结论:我们的提出方法鉴定了来自时间序列基因表达谱的基因规定的转变。动态分析对于对生物系统的深刻理解是必不可少的,并鉴定糖尿病和骨质疏松症的疾病发病的原因。该方法可以大大促进生物学和医学的进展。

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