Kumka Joseph E, Bauer Carl E
Molecular and Cellular Biochemistry Department, Indiana University, Simon Hall MSB, 212 S. Hawthorne Dr, Bloomington, IN, 47405-7003, USA.
BMC Genomics. 2015 Nov 4;16:895. doi: 10.1186/s12864-015-2162-4.
FNR homologues constitute an important class of transcription factors that control a wide range of anaerobic physiological functions in a number of bacterial species. Since FNR homologues are some of the most pervasive transcription factors, an understanding of their involvement in regulating anaerobic gene expression in different species sheds light on evolutionary similarity and differences. To address this question, we used a combination of high throughput RNA-Seq and ChIP-Seq analysis to define the extent of the FnrL regulon in Rhodobacter capsulatus and related our results to that of FnrL in Rhodobacter sphaeroides and FNR in Escherichia coli.
Our RNA-seq results show that FnrL affects the expression of 807 genes, which accounts for over 20 % of the Rba. capsulatus genome. ChIP-seq results indicate that 42 of these genes are directly regulated by FnrL. Importantly, this includes genes involved in the synthesis of the anoxygenic photosystem. Similarly, FnrL in Rba. sphaeroides affects 24 % of its genome, however, only 171 genes are differentially expressed in common between two Rhodobacter species, suggesting significant divergence in regulation.
We show that FnrL in Rba. capsulatus activates photosynthesis while in Rba. sphaeroides FnrL regulation reported to involve repression of the photosystem. This analysis highlights important differences in transcriptional control of photosynthetic events and other metabolic processes controlled by FnrL orthologues in closely related Rhodobacter species. Furthermore, we also show that the E. coli FNR regulon has limited transcriptional overlap with the FnrL regulons from either Rhodobacter species.
FNR 同源物构成了一类重要的转录因子,可控制多种细菌物种中的广泛厌氧生理功能。由于 FNR 同源物是一些最普遍存在的转录因子,了解它们在不同物种中参与调节厌氧基因表达的情况有助于揭示进化上的异同。为了解决这个问题,我们结合高通量 RNA 测序和染色质免疫沉淀测序分析来确定荚膜红细菌中 FnrL 调控子的范围,并将我们的结果与球形红细菌中的 FnrL 以及大肠杆菌中的 FNR 的结果进行比较。
我们的 RNA 测序结果表明,FnrL 影响 807 个基因的表达,占荚膜红细菌基因组的 20% 以上。染色质免疫沉淀测序结果表明,其中 42 个基因受 FnrL 直接调控。重要的是,这包括参与无氧光合系统合成的基因。同样,球形红细菌中的 FnrL 影响其基因组的 24%,然而,在这两种红细菌物种之间只有 171 个基因差异表达,这表明调控存在显著差异。
我们表明,荚膜红细菌中的 FnrL 激活光合作用,而在球形红细菌中,据报道 FnrL 的调控涉及对光合系统的抑制。该分析突出了密切相关的红细菌物种中光合事件和由 FnrL 直系同源物控制的其他代谢过程在转录控制方面的重要差异。此外,我们还表明,大肠杆菌的 FNR 调控子与任一红细菌物种的 FnrL 调控子的转录重叠有限。