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Single-cell RNA sequencing reveals intrinsic and extrinsic regulatory heterogeneity in yeast responding to stress

机译:单细胞RNA测序揭示了酵母对压力的内在和外在调节异质性

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From bacteria to humans, individual cells within isogenic populations can show significant variation in stress tolerance, but the nature of this heterogeneity is not clear. To investigate this, we used single-cell RNA sequencing to quantify transcript heterogeneity in single Saccharomyces cerevisiae cells treated with and without salt stress to explore population variation and identify cellular covariates that influence the stress-responsive transcriptome. Leveraging the extensive knowledge of yeast transcriptional regulation, we uncovered significant regulatory variation in individual yeast cells, both before and after stress. We also discovered that a subset of cells appears to decouple expression of ribosomal protein genes from the environmental stress response in a manner partly correlated with the cell cycle but unrelated to the yeast ultradian metabolic cycle. Live-cell imaging of cells expressing pairs of fluorescent regulators, including the transcription factor Msn2 with Dot6, Sfp1, or MAP kinase Hog1, revealed both coordinated and decoupled nucleocytoplasmic shuttling. Together with transcriptomic analysis, our results suggest that cells maintain a cellular filter against decoupled bursts of transcription factor activation but mount a stress response upon coordinated regulation, even in a subset of unstressed cells. Author summary Genetically identical cells growing in the same environment can vary in their cellular state and behavior. Such heterogeneity may explain why some cells in an isogenic population can survive sudden severe environmental stress whereas other cells succumb. Cell-to-cell variation in gene expression has been linked to variable stress survival, but how and why transcript levels vary across the transcriptome in single cells is only beginning to emerge. Here, we used single-cell RNA sequencing (scRNA-seq) to measure cell-to-cell heterogeneity in the transcriptome of budding yeast ( Saccharomyces cerevisiae ). We find surprising patterns of variation across known sets of transcription factor targets, indicating that cells vary in their transcriptome profile both before and after stress exposure. scRNA-seq analysis combined with live-cell imaging of transcription factor activation dynamics revealed some cells in which the stress response was coordinately activated and other cells in which the traditional response was decoupled, suggesting unrecognized regulatory nuances that expand our understanding of stress response and survival.
机译:从细菌到人类,同基因种群内的单个细胞在压力耐受性上可能表现出显着差异,但这种异质性的性质尚不清楚。为了对此进行研究,我们使用单细胞RNA测序来量化在有盐胁迫和无盐胁迫的情况下,单个酿酒酵母细胞中的转录异质性,以探索种群变异并鉴定影响胁迫响应转录组的细胞共变量。利用酵母转录调控的广泛知识,我们发现应激前后,单个酵母细胞的显着调控差异。我们还发现,细胞的一个子集似乎以与细胞周期部分相关但与酵母超微生物代谢周期无关的方式使核糖体蛋白基因的表达与环境应激反应脱钩。表达成对的荧光调节剂的细胞的活细胞成像,包括具有Dot6,Sfp1或MAP激酶Hog1的转录因子Msn2,揭示了核仁穿梭的协调和解耦。与转录组学分析一起,我们的结果表明,细胞保持了针对解耦的转录因子激活猝发的细胞过滤器,但是即使在未受压力的细胞子集中,也可以通过协调调节产生应激反应。作者摘要在相同环境中生长的遗传上相同的细胞可以在细胞状态和行为方面有所不同。这种异质性可以解释为什么同基因群体中的某些细胞能够在突然的严重环境压力下生存而其他细胞却无法生存。基因表达中的细胞间差异与可变的应激存活率有关,但是单细胞中转录组中转录水平的变化方式和为何以及为什么才开始出现。在这里,我们使用单细胞RNA测序(scRNA-seq)来测量出芽酵母(Saccharomyces cerevisiae)转录组中的细胞间异质性。我们发现转录因子靶标的已知集合之间的变化令人惊讶的模式,表明细胞在应激暴露之前和之后的转录组配置文件中有所不同。 scRNA-seq分析与转录因子激活动态的活细胞成像相结合,揭示了一些应激反应被协同激活的细胞和其他传统应答被解耦的细胞,这表明无法识别的调节细微差别扩大了我们对应激反应和生存的理解。

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