Basan Markus, Zhu Manlu, Dai Xiongfeng, Warren Mya, Sévin Daniel, Wang Yi-Ping, Hwa Terence
Institute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland
Department of Physics, University of California at San Diego, La Jolla, CA, USA State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing, China.
Mol Syst Biol. 2015 Oct 30;11(10):836. doi: 10.15252/msb.20156178.
Understanding how the homeostasis of cellular size and composition is accomplished by different organisms is an outstanding challenge in biology. For exponentially growing Escherichia coli cells, it is long known that the size of cells exhibits a strong positive relation with their growth rates in different nutrient conditions. Here, we characterized cell sizes in a set of orthogonal growth limitations. We report that cell size and mass exhibit positive or negative dependences with growth rate depending on the growth limitation applied. In particular, synthesizing large amounts of "useless" proteins led to an inversion of the canonical, positive relation, with slow growing cells enlarged 7- to 8-fold compared to cells growing at similar rates under nutrient limitation. Strikingly, this increase in cell size was accompanied by a 3- to 4-fold increase in cellular DNA content at slow growth, reaching up to an amount equivalent to ~8 chromosomes per cell. Despite drastic changes in cell mass and macromolecular composition, cellular dry mass density remained constant. Our findings reveal an important role of protein synthesis in cell division control.
了解不同生物体如何实现细胞大小和组成的稳态是生物学中一项重大挑战。对于指数生长的大肠杆菌细胞,长期以来人们都知道,在不同营养条件下,细胞大小与其生长速率呈现出强烈的正相关关系。在此,我们对一组正交生长限制条件下的细胞大小进行了表征。我们报告称,根据所施加的生长限制,细胞大小和质量与生长速率呈现出正相关或负相关。特别地,合成大量“无用”蛋白质导致了典型正相关关系的反转,与在营养限制下以相似速率生长的细胞相比,生长缓慢的细胞增大了7至8倍。引人注目的是,在生长缓慢时,细胞大小的这种增加伴随着细胞DNA含量增加3至4倍,达到每个细胞相当于约8条染色体的量。尽管细胞质量和大分子组成发生了巨大变化,但细胞干质量密度保持不变。我们的研究结果揭示了蛋白质合成在细胞分裂控制中的重要作用。