Gómez-Gómez José-María, Manfredi Candela, Alonso Juan-Carlos, Blázquez Jesús
Departamento de Biotecnología Microbiana, Centro Nacional de Biotecnología, Madrid, Spain.
BMC Biol. 2007 Mar 28;5:14. doi: 10.1186/1741-7007-5-14.
Bacterial motility is a crucial factor in the colonization of natural environments. Escherichia coli has two flagella-driven motility types: swimming and swarming. Swimming motility consists of individual cell movement in liquid medium or soft semisolid agar, whereas swarming is a coordinated cellular behaviour leading to a collective movement on semisolid surfaces. It is known that swimming motility can be influenced by several types of environmental stress. In nature, environmentally induced DNA damage (e.g. UV irradiation) is one of the most common types of stress. One of the key proteins involved in the response to DNA damage is RecA, a multifunctional protein required for maintaining genome integrity and the generation of genetic variation.
The ability of E. coli cells to develop swarming migration on semisolid surfaces was suppressed in the absence of RecA. However, swimming motility was not affected. The swarming defect of a DeltarecA strain was fully complemented by a plasmid-borne recA gene. Although the DeltarecA cells grown on semisolid surfaces exhibited flagellar production, they also presented impaired individual movement as well as a fully inactive collective swarming migration. Both the comparative analysis of gene expression profiles in wild-type and DeltarecA cells grown on a semisolid surface and the motility of lexA1 [Ind-] mutant cells demonstrated that the RecA effect on swarming does not require induction of the SOS response. By using a RecA-GFP fusion protein we were able to segregate the effect of RecA on swarming from its other functions. This protein fusion failed to regulate the induction of the SOS response, the recombinational DNA repair of UV-treated cells and the genetic recombination, however, it was efficient in rescuing the swarming motility defect of the DeltarecA mutant. The RecA-GFP protein retains a residual ssDNA-dependent ATPase activity but does not perform DNA strand exchange.
The experimental evidence presented in this work supports a novel role for RecA: the promotion of swarming motility. The defective swarming migration of DeltarecA cells does not appear to be associated with defective flagellar production; rather, it seems to be associated with an abnormal flagellar propulsion function. Our results strongly suggest that the RecA effect on swarming motility does not require an extensive canonical RecA nucleofilament formation. RecA is the first reported cellular factor specifically affecting swarming but not swimming motility in E. coli. The integration of two apparently disconnected biologically important processes, such as the maintenance of genome integrity and motility in a unique protein, may have important evolutive consequences.
细菌运动性是在自然环境中定殖的关键因素。大肠杆菌有两种由鞭毛驱动的运动类型:游动和群游。游动运动性是指单个细胞在液体培养基或软半固体琼脂中的运动,而群游是一种协调的细胞行为,导致在半固体表面的集体运动。已知游动运动性会受到几种环境压力的影响。在自然界中,环境诱导的DNA损伤(如紫外线照射)是最常见的压力类型之一。参与DNA损伤应答的关键蛋白之一是RecA,它是维持基因组完整性和产生遗传变异所需的多功能蛋白。
在缺乏RecA的情况下,大肠杆菌细胞在半固体表面形成群游迁移的能力受到抑制。然而,游动运动性不受影响。携带质粒的recA基因完全弥补了ΔrecA菌株的群游缺陷。虽然在半固体表面生长的ΔrecA细胞表现出鞭毛产生,但它们的个体运动也受损,并且集体群游迁移完全无活性。对在半固体表面生长的野生型和ΔrecA细胞的基因表达谱进行比较分析以及lexA1[Ind-]突变细胞的运动性分析均表明,RecA对群游的影响不需要诱导SOS应答。通过使用RecA-GFP融合蛋白,我们能够将RecA对群游的影响与其其他功能区分开来。这种蛋白融合未能调节SOS应答的诱导、紫外线处理细胞的重组DNA修复和基因重组,然而,它有效地挽救了ΔrecA突变体的群游运动性缺陷。RecA-GFP蛋白保留了残余的单链DNA依赖性ATP酶活性,但不进行DNA链交换。
本研究提供的实验证据支持RecA的一种新作用:促进群游运动性。ΔrecA细胞群游迁移缺陷似乎与鞭毛产生缺陷无关;相反,它似乎与异常的鞭毛推进功能有关。我们的结果强烈表明,RecA对群游运动性的影响不需要广泛形成典型的RecA核丝。RecA是第一个被报道的特异性影响大肠杆菌群游而不影响游动运动性的细胞因子。将两个明显不相关的生物学重要过程,如基因组完整性的维持和运动性,整合到一个独特的蛋白质中,可能具有重要的进化意义。