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Effect of global translation initiation inhibition associated to glucose starvation on cytoplasmic lncRNAs levels

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To analyze the effect of global translation initiation inhibition associated to glucose deprivation on cytoplasmic lncRNAs levels, we performed RNA-Seq using WT, xrn1-delta and upf1-delta cells grown in glucose-containing complete synthetic medium (CSM) and then shifted for 16 min in glycerol- and ethanol-containing medium. In parallel, control cells were maintained for the same time in glucose-containing CSM. For the WT strains, we also included a treatment of 15 min with CHX (100 μg/ml final concentration) or an equal volume of DMSO (Mock).

为探究葡萄糖剥夺相关的全局翻译起始抑制对细胞质长链非编码RNA(lncRNAs)水平的影响,我们针对在含葡萄糖的完全合成培养基(CSM)中培养、随后转移至含甘油与乙醇的培养基中孵育16分钟的野生型(WT)、xrn1Δ与upf1Δ细胞开展了RNA测序(RNA-Seq)实验。与此同时,对照组细胞在含葡萄糖的CSM中维持相同培养时长。针对野生型菌株,我们还设置了终浓度为100 μg/ml的环己酰亚胺(CHX)处理15分钟的实验组,以及加入等体积二甲基亚砜(DMSO)的空白对照(Mock)组。

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