Petersen Lise, Bollback Jonathan P, Dimmic Matt, Hubisz Melissa, Nielsen Rasmus
Bioinformatics Centre, University of Copenhagen, Copenhagen DK-2200, Denmark.
Genome Res. 2007 Sep;17(9):1336-43. doi: 10.1101/gr.6254707. Epub 2007 Aug 3.
We used a comparative genomics approach to identify genes that are under positive selection in six strains of Escherichia coli and Shigella flexneri, including five strains that are human pathogens. We find that positive selection targets a wide range of different functions in the E. coli genome, including cell surface proteins such as beta barrel porins, presumably because of the involvement of these genes in evolutionary arms races with other bacteria, phages, and/or the host immune system. Structural mapping of positively selected sites on trans-membrane beta barrel porins reveals that the residues under positive selection occur almost exclusively in the extracellular region of the proteins that are enriched with sites known to be targets of phages, colicins, or the host immune system. More surprisingly, we also find a number of other categories of genes that show very strong evidence for positive selection, such as the enigmatic rhs elements and transposases. Based on structural evidence, we hypothesize that the selection acting on transposases is related to the genomic conflict between transposable elements and the host genome.
我们采用比较基因组学方法,在包括5种人类病原体菌株在内的6株大肠杆菌和福氏志贺氏菌中鉴定受到正选择的基因。我们发现,正选择作用于大肠杆菌基因组中广泛的不同功能,包括细胞表面蛋白如β桶状孔蛋白,推测是因为这些基因参与了与其他细菌、噬菌体和/或宿主免疫系统的进化军备竞赛。对跨膜β桶状孔蛋白上正选择位点的结构定位显示,正选择的残基几乎只出现在蛋白质的细胞外区域,该区域富含已知为噬菌体、大肠杆菌素或宿主免疫系统靶点的位点。更令人惊讶的是,我们还发现许多其他类别的基因有非常强的正选择证据,如神秘的rhs元件和转座酶。基于结构证据,我们推测作用于转座酶的选择与转座元件和宿主基因组之间的基因组冲突有关。