Department of Biochemistry, The University of Texas Southwestern Medical Center, Dallas, Texas 75390-9038, USA.
Mol Microbiol. 2010 May;76(3):559-75. doi: 10.1111/j.1365-2958.2010.07131.x. Epub 2010 Mar 31.
Formation of a Bacillus subtilis biofilm community requires an abundant matrix protein, TasA and an exopolysaccharide. The transcriptional regulatory pathways that control synthesis of these structural features are complex and responsive to multiple physiological and population signals. We report herein that an additional layer of co-transcriptional regulation is required for exopolysaccharide (eps) expression. This mechanism is mediated by a novel cis-acting RNA element, coined 'EAR', located between the second and third gene of the eps operon. The presence of the EAR element within the eps operon is required for readthrough of distally located termination signals. We also find that the EAR element promotes readthrough of heterologous termination sites. Based upon these observations, we hypothesize that the EAR element associates with RNA polymerase to promote processive antitermination, a process wherein the transcription elongation complex is altered by accessory factors to become resistant to pausing and termination signals. It is likely that this mechanism is required for eps expression to ensure full synthesis of the unusually long transcript (16 kb). We also identify the EAR element in other species within the order Bacillales, suggesting that a similar mechanism is required for synthesis of biofilm and capsular polysaccharide operons in other microorganisms.
枯草芽孢杆菌生物膜群落的形成需要丰富的基质蛋白 TasA 和胞外多糖。控制这些结构特征合成的转录调控途径非常复杂,对多种生理和群体信号有响应。本文报道了一种额外的共转录调控层,用于调节胞外多糖 (eps) 的表达。这种机制是由一个新的顺式作用 RNA 元件介导的,称为“EAR”,位于 eps 操纵子的第二和第三个基因之间。在 eps 操纵子中存在 EAR 元件是通读远程终止信号所必需的。我们还发现 EAR 元件促进了异源终止位点的通读。基于这些观察,我们假设 EAR 元件与 RNA 聚合酶结合,以促进连续抗终止,这是一个转录延伸复合物被辅助因子改变以抵抗暂停和终止信号的过程。这种机制可能是 eps 表达所必需的,以确保异常长的转录本(16kb)的完全合成。我们还在芽孢杆菌目中的其他物种中鉴定出 EAR 元件,表明在其他微生物中,合成生物膜和荚膜多糖操纵子也需要类似的机制。