Department of Microbial Pathogenesis, Yale School of Medicine, New Haven, Connecticut, USA.
Yale Microbial Sciences Institute, West Haven, Connecticut, USA.
Bioessays. 2023 Oct;45(10):e2300062. doi: 10.1002/bies.202300062. Epub 2023 Aug 3.
Horizontal gene transfer advances bacterial evolution. To benefit from horizontally acquired genes, enteric bacteria must overcome silencing caused when the widespread heat-stable nucleoid structuring (H-NS) protein binds to AT-rich horizontally acquired genes. This ability had previously been ascribed to both anti-silencing proteins outcompeting H-NS for binding to AT-rich DNA and RNA polymerase initiating transcription from alternative promoters. However, we now know that pathogenic Salmonella enterica serovar Typhimurium and commensal Escherichia coli break down H-NS when this silencer is not bound to DNA. Curiously, both species use the same protease - Lon - to destroy H-NS in distinct environments. Anti-silencing proteins promote the expression of horizontally acquired genes without binding to them by displacing H-NS from AT-rich DNA, thus leaving H-NS susceptible to proteolysis and decreasing H-NS amounts overall. Conserved amino acid sequences in the Lon protease and H-NS cleavage site suggest that diverse bacteria degrade H-NS to exploit horizontally acquired genes.
水平基因转移促进了细菌的进化。为了从水平获得的基因中获益,肠道细菌必须克服由于广泛存在的热稳定核基质结构(H-NS)蛋白与富含 AT 的水平获得基因结合而导致的沉默。这种能力以前归因于抗沉默蛋白与 H-NS 竞争结合富含 AT 的 DNA 和 RNA 聚合酶从替代启动子起始转录。然而,我们现在知道,致病性沙门氏菌血清型鼠伤寒和共生大肠杆菌在沉默因子未与 DNA 结合时会分解 H-NS。奇怪的是,这两个物种都使用相同的蛋白酶 Lon 来在不同的环境中破坏 H-NS。抗沉默蛋白通过将 H-NS 从富含 AT 的 DNA 上置换出来,促进水平获得基因的表达,而无需与它们结合,从而使 H-NS 易于蛋白水解,并降低 H-NS 的总量。Lon 蛋白酶和 H-NS 切割位点中的保守氨基酸序列表明,不同的细菌通过降解 H-NS 来利用水平获得的基因。