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Evolutionary model for the unequal segregation of high copy plasmids

机译:高拷贝质粒不平等分离的进化模型

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Author summary In the last years, it becomes more and more clear that heterogeneity in isogenic bacterial populations is rather the rule than the exception. This observation is interesting as it reveals the complex social life of bacteria, and also because of tremendous practical implications in medicine, biotechnology, and ecology. The central questions in this field are the identification of the underlying proximate causes (molecular mechanisms) on the one hand and on the other hand the identification of ultimate causes (evolutionary forces) that shape the social life of bacteria. We focus on plasmid dynamics, in particular on plasmid segregation. Recent experiments showed that plasmid segregation depends on the plasmid load. We identify possible evolutionary factors that shaped this process. It turns out that the ambivalence in the effect of plasmidsadvantageous if present in low copy numbers, a metabolic burden if present in high copy numbersis able to explain the experimental observations. The experimental findings can be interpreted as a variant of the principle of division of labor, as it is well known from e.g. persister cells or sporulation. Our model extends the theory of unequal segregation of damage to the ambivalent role of plasmids. Similarly, it is known that certain gene regulatory proteins are acting in a dose-dependent manner. Due to differences in their cellular concentrations and in their affinities to various target promoters, differential gene expression patterns are achieved. Consequently, tight concentration control is observed [1]. Another example is the strict copy-dependent utilization of autolysins during cell division. These enzymes carefully open the bacterial cell wall to allow for its extension [2]. Overproduction of these enzymes leads to cell lysis [3]. These molecules are in principle also candidates for a segregation characteristic similar to that of high copy plasmids described here.
机译:作者总结在过去的几年中,越来越清楚的是,同基因细菌种群中的异质性是规则而不是例外。这一发现很有趣,因为它揭示了细菌的复杂社会生活,并且还因为它在医学,生物技术和生态学方面具有巨大的实际意义。该领域的中心问题一方面是确定潜在的近因(分子机制),另一方面是确定影响细菌社会生活的最终原因(进化力)。我们专注于质粒动力学,特别是质粒分离。最近的实验表明,质粒分离取决于质粒的负载。我们确定了可能影响这一过程的进化因素。事实证明,如果以低拷贝数存在,则质粒作用的矛盾性是有利的;如果以高拷贝数存在,则质粒代谢的负担是可以解释实验观察结果的。实验发现可以解释为分工原理的一种变体,如从例如美国专利No.5,No.5,No.5,No.5,No.5,No.4,1999,2,3,4,5,6,5,6,5,5,6,5,5,6中可以看出。持续性细胞或孢子形成。我们的模型将不均等的损伤分离理论扩展到质粒的矛盾作用。类似地,已知某些基因调节蛋白以剂量依赖性方式起作用。由于它们的细胞浓度及其与各种靶启动子的亲和力的差异,获得了差异的基因表达模式。因此,观察到严格的浓度控制[1]。另一个例子是细胞分裂过程中自溶素的严格拷贝依赖性利用。这些酶小心地打开细菌细胞壁以使其延伸[2]。这些酶的过度生产导致细胞裂解[3]。这些分子原则上也是与本文所述的高拷贝质粒相似的分离特征的候选物。

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