Department of Microbiology, University of Georgia, Athens, GA, 30602, USA.
BMC Genomics. 2018 Jan 16;19(1):52. doi: 10.1186/s12864-017-4413-z.
The protean chemical properties of mercury have long made it attractive for diverse applications, but its toxicity requires great care in its use, disposal, and recycling. Mercury occurs in multiple chemical forms, and the molecular basis for the distinct toxicity of its various forms is only partly understood. Global transcriptomics applied over time can reveal how a cell recognizes a toxicant and what cellular subsystems it marshals to repair and recover from the damage. The longitudinal effects on the transcriptome of exponential phase E. coli were compared during sub-acute exposure to mercuric chloride (HgCl) or to phenylmercuric acetate (PMA) using RNA-Seq.
Differential gene expression revealed common and distinct responses to the mercurials throughout recovery. Cultures exhibited growth stasis immediately after each mercurial exposure but returned to normal growth more quickly after PMA exposure than after HgCl exposure. Correspondingly, PMA rapidly elicited up-regulation of a large number of genes which continued for 30 min, whereas fewer genes were up-regulated early after HgCl exposure only some of which overlapped with PMA up-regulated genes. By 60 min gene expression in PMA-exposed cells was almost indistinguishable from unexposed cells, but HgCl exposed cells still had many differentially expressed genes. Relative expression of energy production and most metabolite uptake pathways declined with both compounds, but nearly all stress response systems were up-regulated by one or the other mercurial during recovery.
Sub-acute exposure influenced expression of ~45% of all genes with many distinct responses for each compound, reflecting differential biochemical damage by each mercurial and the corresponding resources available for repair. This study is the first global, high-resolution view of the transcriptional responses to any common toxicant in a prokaryotic model system from exposure to recovery of active growth. The responses provoked by these two mercurials in this model bacterium also provide insights about how higher organisms may respond to these ubiquitous metal toxicants.
汞具有多变的化学性质,长期以来一直受到各种应用的青睐,但由于其毒性,在使用、处置和回收过程中需要格外小心。汞以多种化学形式存在,其各种形式毒性的分子基础部分被理解。随着时间的推移,全球转录组学可以揭示细胞如何识别毒物,以及它动员哪些细胞子系统来修复和从损伤中恢复。本研究使用 RNA-Seq 比较了指数生长期大肠杆菌在亚急性暴露于氯化汞(HgCl)或苯汞乙酸盐(PMA)过程中,转录组的纵向变化。
差异基因表达揭示了两种汞剂在整个恢复过程中的共同和独特反应。暴露后,各培养物的生长立即停滞,但 PMA 暴露后比 HgCl 暴露后更快地恢复到正常生长。相应地,PMA 迅速诱导大量基因上调,这种上调持续 30 分钟,而 HgCl 暴露后早期仅有少数基因上调,其中一些与 PMA 上调基因重叠。到 60 分钟时,PMA 暴露细胞的基因表达几乎与未暴露细胞无法区分,但 HgCl 暴露细胞仍有许多差异表达基因。两种化合物都使能量产生和大多数代谢物摄取途径的相对表达下降,但几乎所有应激反应系统在恢复过程中都被一种或另一种汞剂上调。
亚急性暴露影响了约 45%的所有基因的表达,每种化合物都有许多不同的反应,反映了每种汞剂的不同生化损伤和相应的修复资源。这项研究是在原核模型系统中,从暴露到恢复活性生长,对任何常见毒物的转录反应进行的首次全面、高分辨率观察。该模型细菌中这两种汞剂引起的反应也为高等生物可能对这些普遍存在的金属毒物做出的反应提供了一些见解。