Department of Medical Biochemistry and Microbiology, Uppsala University, Sweden.
Department of Cell and Molecular Biology, Uppsala University, Sweden.
Genome Biol Evol. 2022 Oct 7;14(10). doi: 10.1093/gbe/evac135.
Conjugation driven by a chromosomally integrated F-plasmid (high frequency of recombination strain) can create bacteria with hybrid chromosomes. Previous studies of interspecies hybrids have focused on hybrids in which a region of donor chromosome replaces an orthologous region of recipient chromosome leaving chromosome size unchanged. Very little is known about hybrids with enlarged chromosomes, the mechanisms of their creation, or their subsequent trajectories of adaptative evolution. We addressed this by selecting 11 interspecies hybrids between Escherichia coli and Salmonella Typhimurium in which genome size was enlarged. In three cases, this occurred by the creation of an F'-plasmid while in the remaining eight, it was due to recombination of donor DNA into the recipient chromosome. Chromosome length increased by up to 33% and was associated in most cases with reduced growth fitness. Two hybrids, in which chromosome length was increased by the addition of 0.97 and 1.3 Mb, respectively, were evolved to study genetic pathways of fitness cost amelioration. In each case, relative fitness rapidly approached one and this was associated with large deletions involving recombination between repetitive DNA sequences. The locations of these repetitive sequences played a major role in determining the architecture of the evolved genotypes. Notably, in ten out of ten independent evolution experiments, deletions removed DNA of both species, creating high-fitness strains with hybrid chromosomes. In conclusion, we found that enlargement of a bacterial chromosome by acquisition of diverged orthologous DNA is followed by a period of rapid evolutionary adjustment frequently creating irreversibly hybrid chromosomes.
由染色体整合的 F 质粒驱动的杂交(高频重组菌株)可产生具有杂交染色体的细菌。先前的种间杂种研究主要集中在供体染色体的一个区域取代受体染色体的同源区域,而染色体大小不变的杂种上。对于染色体增大的杂种、它们的产生机制及其随后的适应性进化轨迹,人们知之甚少。我们通过在大肠杆菌和鼠伤寒沙门氏菌之间选择 11 种基因组大小增大的种间杂种来解决这个问题。在三种情况下,这是通过创建 F'-质粒来实现的,而在其余八种情况下,这是由于供体 DNA 重组到受体染色体中。染色体长度增加了高达 33%,并且在大多数情况下与生长适应性降低有关。两个杂种的染色体长度分别增加了 0.97 和 1.3 Mb,分别进化以研究适应性成本缓解的遗传途径。在每种情况下,相对适应性迅速接近 1,这与涉及重复 DNA 序列之间重组的大缺失有关。这些重复序列的位置在确定进化基因型的结构方面起着重要作用。值得注意的是,在十个独立的进化实验中,缺失都去除了两个物种的 DNA,产生了具有杂交染色体的高适应性菌株。总之,我们发现,通过获得分化的直系同源 DNA 来扩大细菌染色体,随后会经历一个快速进化调整的时期,经常会产生不可逆转的杂交染色体。