Higgins N Patrick
Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, 720 20th Street South, Kaul Human Genetics Bldg. 524a, Birmingham, AL, 35233, USA.
Biophys Rev. 2016 Nov;8(Suppl 1):113-121. doi: 10.1007/s12551-016-0207-9. Epub 2016 Jul 20.
Bacteria organize DNA into self-adherent conglomerates called nucleoids that are replicated, transcribed, and partitioned within the cytoplasm during growth and cell division. Three classes of proteins help condense nucleoids: (1) DNA gyrase generates diffusible negative supercoils that help compact DNA into a dynamic interwound and multiply branched structure; (2) RNA polymerase and abundant small basic nucleoid-associated proteins (NAPs) create constrained supercoils by binding, bending, and forming cooperative protein-DNA complexes; (3) a multi-protein DNA condensin organizes chromosome structure to assist sister chromosome segregation after replication. Most bacteria have four topoisomerases that participate in DNA dynamics during replication and transcription. Gyrase and topoisomerase I (Topo I) are intimately involved in transcription; Topo III and Topo IV play critical roles in decatenating and unknotting DNA during and immediately after replication. RNA polymerase generates positive (+) supercoils downstream and negative (-) supercoils upstream of highly transcribed operons. Supercoil levels vary under fast versus slow growth conditions, but what surprises many investigators is that it also varies significantly between different bacterial species. The MukFEB condensin is dispensable in the high supercoil density (σ) organism Escherichia coli but is essential in Salmonella spp. which has 15 % fewer supercoils. These observations raise two questions: (1) How do different species regulate supercoil density? (2) Why do closely related species evolve different optimal supercoil levels? Control of supercoil density in E. coli and Salmonella is largely determined by differences encoded within the gyrase subunits. Supercoil differences may arise to minimalize toxicity of mobile DNA elements in the genome.
细菌将DNA组织成称为类核的自我附着聚集体,在生长和细胞分裂过程中,类核在细胞质内进行复制、转录和分配。三类蛋白质有助于浓缩类核:(1)DNA促旋酶产生可扩散的负超螺旋,有助于将DNA压缩成动态的相互缠绕和多分支结构;(2)RNA聚合酶和丰富的小碱性类核相关蛋白(NAPs)通过结合、弯曲和形成协同的蛋白质-DNA复合物来产生受限超螺旋;(3)一种多蛋白DNA凝聚素组织染色体结构,以协助复制后姐妹染色体的分离。大多数细菌有四种拓扑异构酶,它们在复制和转录过程中参与DNA动态变化。促旋酶和拓扑异构酶I(Topo I)密切参与转录;拓扑异构酶III和拓扑异构酶IV在复制期间及复制后立即解开DNA连环和结中起关键作用。RNA聚合酶在高度转录的操纵子下游产生正(+)超螺旋,在上游产生负(-)超螺旋。超螺旋水平在快速生长与缓慢生长条件下有所不同,但令许多研究人员惊讶的是,不同细菌物种之间超螺旋水平也有显著差异。MukFEB凝聚素在超高螺旋密度(σ)的生物体大肠杆菌中是可有可无的,但在超螺旋少15%的沙门氏菌属中却是必不可少的。这些观察结果提出了两个问题:(1)不同物种如何调节超螺旋密度?(2)为什么亲缘关系密切的物种会进化出不同的最佳超螺旋水平?大肠杆菌和沙门氏菌中超螺旋密度的控制很大程度上由促旋酶亚基内编码的差异决定。超螺旋差异可能是为了使基因组中移动DNA元件的毒性最小化而产生的。