Institute of Biogeochemistry and Pollutant Dynamics, Department of Environmental Systems Science, ETH Zurich, 8092 Zurich, Switzerland; Department of Environmental Microbiology, Eawag, 8600 Dübendorf, Switzerland.
Institute of Biogeochemistry and Pollutant Dynamics, Department of Environmental Systems Science, ETH Zurich, 8092 Zurich, Switzerland; Department of Environmental Microbiology, Eawag, 8600 Dübendorf, Switzerland.
Cell Syst. 2018 Apr 25;6(4):496-507.e6. doi: 10.1016/j.cels.2018.03.009. Epub 2018 Apr 11.
Gene expression levels in clonal bacterial groups have been found to be spatially correlated. These correlations can partly be explained by the shared lineage history of nearby cells, although they could also arise from local cell-cell interactions. Here, we present a quantitative framework that allows us to disentangle the contributions of lineage history, long-range spatial gradients, and local cell-cell interactions to spatial correlations in gene expression. We study pathways involved in toxin production, SOS stress response, and metabolism in Escherichia coli microcolonies and find for all pathways that shared lineage history is the main cause of spatial correlations in gene expression levels. However, long-range spatial gradients and local cell-cell interactions also contributed to spatial correlations in SOS response, amino acid biosynthesis, and overall metabolic activity. Together, our data show that the phenotype of a cell is influenced by its lineage history and population context, raising the question of whether bacteria can arrange their activities in space to perform functions they cannot achieve alone.
已发现克隆细菌群体中的基因表达水平存在空间相关性。这些相关性部分可以通过附近细胞的共享谱系历史来解释,尽管它们也可能来自于局部细胞间的相互作用。在这里,我们提出了一个定量框架,使我们能够区分谱系历史、长程空间梯度和局部细胞间相互作用对基因表达空间相关性的贡献。我们研究了大肠杆菌微菌落中涉及毒素产生、SOS 应激反应和代谢的途径,发现对于所有途径,共享的谱系历史是基因表达水平空间相关性的主要原因。然而,长程空间梯度和局部细胞间相互作用也导致了 SOS 反应、氨基酸生物合成和整体代谢活性的空间相关性。总的来说,我们的数据表明,细胞的表型受到其谱系历史和群体背景的影响,这引发了一个问题,即细菌是否可以在空间上安排它们的活动,以执行它们单独无法完成的功能。