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Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and Smad7-/- E15.5 tooth germ Transcriptomes

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Smad7 is known to regulate both Smad-dependent and Smad-independent TGF-beta signaling pathways but is also extensively involved in crosstalks with other signaling pathways. To investigate the underlying molecular mechanism, we conducted RNA-Seq analysis on E15.5 molars from Smad7 mutant and control mice. Tooth germ mRNA profiles of E15.5 wild type (WT) and Smad7-/- mice were generated by deep sequencing, in triplicate, using Illumina NextSeq 550.

Smad7 已知可同时调控Smad依赖型与Smad非依赖型转化生长因子-β(transforming growth factor-β, TGF-β)信号通路,且广泛参与与其他信号通路的交叉对话。为探究其潜在的分子机制,我们对Smad7敲除突变型与对照小鼠的E15.5胎龄磨牙开展了RNA测序(RNA-Seq)分析。本研究采用Illumina NextSeq 550平台进行三次生物学重复的深度测序,获取了E15.5胎龄野生型(wild type, WT)与Smad7敲除(Smad7-/-)小鼠的牙胚mRNA表达谱。

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