Papadopoulos D, Schneider D, Meier-Eiss J, Arber W, Lenski R E, Blot M
Abteilung Mikrobiologie, Biozentrum, CH-4056 Basel, Switzerland.
Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3807-12. doi: 10.1073/pnas.96.7.3807.
Molecular methods are used widely to measure genetic diversity within populations and determine relationships among species. However, it is difficult to observe genomic evolution in action because these dynamics are too slow in most organisms. To overcome this limitation, we sampled genomes from populations of Escherichia coli evolving in the laboratory for 10,000 generations. We analyzed the genomes for restriction fragment length polymorphisms (RFLP) using seven insertion sequences (IS) as probes; most polymorphisms detected by this approach reflect rearrangements (including transpositions) rather than point mutations. The evolving genomes became increasingly different from their ancestor over time. Moreover, tremendous diversity accumulated within each population, such that almost every individual had a different genetic fingerprint after 10,000 generations. As has been often suggested, but not previously shown by experiment, the rates of phenotypic and genomic change were discordant, both across replicate populations and over time within a population. Certain pivotal mutations were shared by all descendants in a population, and these are candidates for beneficial mutations, which are rare and difficult to find. More generally, these data show that the genome is highly dynamic even over a time scale that is, from an evolutionary perspective, very brief.
分子方法被广泛用于测量种群内的遗传多样性并确定物种间的关系。然而,很难观察到基因组进化的实际过程,因为在大多数生物体中这些动态变化过于缓慢。为了克服这一限制,我们从在实验室中进化了10000代的大肠杆菌种群中采样基因组。我们使用七个插入序列(IS)作为探针分析基因组的限制性片段长度多态性(RFLP);通过这种方法检测到的大多数多态性反映的是重排(包括转座)而非点突变。随着时间的推移,进化的基因组与其祖先越来越不同。此外,每个种群内部积累了巨大的多样性,以至于在10000代之后几乎每个个体都有不同的遗传指纹。正如人们经常所认为的,但之前并未通过实验证明,表型和基因组变化的速率在重复种群之间以及种群内部随时间都是不一致的。一个种群中的所有后代都共享某些关键突变,这些突变是有益突变的候选者,而有益突变既罕见又难以找到。更普遍地说,这些数据表明,即使从进化的角度来看是非常短暂的时间尺度上,基因组也是高度动态的。