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Threshold effect of growth rate on population variability of Escherichia coli cell lengths

机译:增长率的阈值效应对大肠杆菌细胞长度的群体变异性的影响

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摘要

A long-standing question in biology is the effect of growth on cell size. Here, we estimate the effect of Escherichia coli growth rate (r) on population cell size distributions by estimating the coefficient of variation of cell lengths (CVL) from image analysis of fixed cells in DIC microscopy. We find that the CVL is constant at growth rates less than one division per hour, whereas above this threshold, CVL increases with an increase in the growth rate. We hypothesize that stochastic inhibition of cell division owing to replication stalling by a RecA-dependent mechanism, combined with the growth rate threshold of multi-fork replication (according to Cooper and Helmstetter), could form the basis of such a threshold effect. We proceed to test our hypothesis by increasing the frequency of stochastic stalling of replication forks with hydroxyurea (HU) treatment and find that cell length variability increases only when the growth rate exceeds this threshold. The population effect is also reproduced in single-cell studies using agar-pad cultures and ‘mother machine’-based experiments to achieve synchrony. To test the role of RecA, critical for the repair of stalled replication forks, we examine the CVL of E. coli ΔrecA cells. We find cell length variability in the mutant to be greater than wild-type, a phenotype that is rescued by plasmid-based RecA expression. Additionally, we find that RecA-GFP protein recruitment to nucleoids is more frequent at growth rates exceeding the growth rate threshold and is further enhanced on HU treatment. Thus, we find growth rates greater than a threshold result in increased E. coli cell lengths in the population, and this effect is, at least in part, mediated by RecA recruitment to the nucleoid and stochastic inhibition of division.
机译:生物学中一个长期存在的问题是生长对细胞大小的影响。在这里,我们通过从DIC显微镜下固定细胞的图像分析中估计细胞长度的变异系数(CVL)来估计大肠杆菌生长速率(r)对种群细胞大小分布的影响。我们发现CVL在每小时小于一格的增长率下是恒定的,而在此阈值之上,CVL随着增长率的增加而增加。我们假设由于RecA依赖性机制的复制停滞而对细胞分裂的随机抑制,再加上多叉复制的增长率阈值(根据Cooper和Helmstetter的研究),可以构成这种阈值效应的基础。我们通过用羟基脲(HU)处理增加复制叉的随机停转频率来检验我们的假设,并发现仅当生长速率超过此阈值时,细胞长度变异性才会增加。在单细胞研究中,使用琼脂垫培养物和基于“母机”的实验也获得了种群效应,以实现同步。为了测试对修复停滞的复制叉至关重要的RecA的作用,我们检查了大肠杆菌ΔrecA细胞的CVL。我们发现突变体中的细胞长度变异性大于野生型,这是一种基于质粒的RecA表达挽救的表型。此外,我们发现RecA-GFP蛋白募集到类核苷的生长速率超过生长速率阈值时更为频繁,并且在HU治疗中得到进一步增强。因此,我们发现增长率大于阈值会导致种群中大肠杆菌细胞长度增加,并且这种影响至少部分是由RecA募集到核苷和随机抑制分裂介导的。

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