Aas Finn Erik, Wolfgang Matthew, Frye Stephan, Dunham Steven, Løvold Cecilia, Koomey Michael
Biotechnology Centre of Oslo, University of Oslo, 0316 Oslo, Norway.
Mol Microbiol. 2002 Nov;46(3):749-60. doi: 10.1046/j.1365-2958.2002.03193.x.
The mechanisms by which DNA is taken up into the bacterial cell during natural genetic transformation are poorly understood. Although related components essential to the uptake of DNA during transformation have been defined in Gram-negative species, it remains unclear whether DNA binding and uptake are dissociable events. Therefore, DNA uptake has been the earliest definable step in any Gram-negative transformation pathway. In the human pathogen Neisseria gonorrhoeae, sequence-specific DNA uptake requires an intact type IV pili (Tfp) biogenesis machinery along with three molecules that are dispensable for Tfp expression: ComP (a pilin subunit-like molecule), PilT (a cytoplasmic protein involved in pilus retraction) and ComE (a periplasmic protein with intrinsic DNA-binding activity). By conditionally altering the levels of ComP and PilT expression, we show here that DNA binding and uptake are resolvable events. Consequently, we are able to demonstrate that PilT is largely dispensable for functional DNA binding and, therefore, contributes specifically to uptake. Furthermore, sequence specificity in this system is imposed at the level of DNA binding, a process that is influenced by both ComP and PilE. However, sequence-specific DNA binding is not attributable to an intrinsic property of the Tfp subunit protein. Finally, we demonstrate the existence of a robust, non-specific DNA-binding activity associated with the expression of both Tfp and PilT, which is unrelated to transformation but obscures the observation of specific binding events.
在自然遗传转化过程中,DNA进入细菌细胞的机制尚不清楚。尽管在革兰氏阴性菌中已经确定了转化过程中DNA摄取所必需的相关成分,但DNA结合和摄取是否为可分离的事件仍不清楚。因此,DNA摄取一直是任何革兰氏阴性菌转化途径中最早可定义的步骤。在人类病原体淋病奈瑟菌中,序列特异性DNA摄取需要完整的IV型菌毛(Tfp)生物合成机制以及三种对Tfp表达可有可无的分子:ComP(一种菌毛蛋白亚基样分子)、PilT(一种参与菌毛回缩的胞质蛋白)和ComE(一种具有内在DNA结合活性的周质蛋白)。通过有条件地改变ComP和PilT的表达水平,我们在此表明DNA结合和摄取是可分辨的事件。因此,我们能够证明PilT在很大程度上对于功能性DNA结合是可有可无的,因此,它对摄取有特异性贡献。此外,该系统中的序列特异性是在DNA结合水平上施加的,这一过程受到ComP和PilE两者的影响。然而,序列特异性DNA结合并非归因于Tfp亚基蛋白的内在特性。最后,我们证明了与Tfp和PilT表达相关的一种强大的非特异性DNA结合活性的存在,它与转化无关,但掩盖了特异性结合事件的观察。