Expression of the Cyanobacterial FoF1 ATP Synthase Regulator AtpΘ Depends on Small DNA-Binding Proteins and Differential mRNA Stability

被引:8
|
作者
Song, Kuo [1 ,4 ]
Hagemann, Martin [2 ]
Georg, Jens [1 ]
Maass, Sandra [3 ]
Becher, Doerte [3 ]
Hess, Wolfgang R. [1 ]
机构
[1] Univ Freiburg, Genet & Expt Bioinformat, Fac Biol, Freiburg, Germany
[2] Univ Rostock, Inst Biol Sci, Plant Physiol Dept, Rostock, Germany
[3] Univ Greifswald, Inst Microbiol, Ctr Funct Genom Microbes, Dept Microbial Prote, Greifswald, Germany
[4] Univ Freiburg, Inst Biochem & Mol Biol, ZBMZ, Fac Med, Freiburg, Germany
来源
MICROBIOLOGY SPECTRUM | 2022年 / 10卷 / 03期
关键词
FoF1 ATP synthase; Atp Theta; cyanobacteria; cyAbrBs; transcriptional regulation; RNA stability; RpaB; SP PCC 6803; TRANSCRIPTIONAL REGULATOR; GENE-EXPRESSION; SYNECHOCYSTIS; ABRB; METABOLISM; INHIBITOR; GAMMA; REVEALS; SLL0822;
D O I
10.1128/spectrum.02562-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
FoF1 ATP synthases produce ATP, the universal biological energy source. Under unfavorable conditions, ATP synthases can operate in a futile reverse reaction, pumping protons while ATP is used up. ABSTRACT FoF1 ATP synthases produce ATP, the universal biological energy source. ATP synthase complexes on cyanobacterial thylakoid membranes use proton gradients generated either by photosynthesis or respiration. Atp Theta is an ATP synthase regulator in cyanobacteria which is encoded by the gene atpT. Atp Theta prevents the hydrolysis of ATP (reverse reaction) that otherwise would occur under unfavorable conditions. In the cyanobacterium Synechocystis sp. PCC 6803, Atp Theta is expressed maximum in darkness but at very low levels under optimum phototrophic growth conditions or in the presence of glucose. DNA coimmunoprecipitation experiments followed by mass spectrometry identified the binding of the two transcriptional regulators cyAbrB1 and cyAbrB2 to the promoter and the histone-like protein HU to the 5'UTR of atpT. Analyses of nucleotide substitutions in the promoter and GFP reporter assays identified a functionally relevant sequence motif resembling the HLR1 element bound by the RpaB transcription factor. Electrophoretic mobility shift assays confirmed interaction of cyAbrB1, cyAbrB2, and RpaB with the promoter DNA. However, overall the effect of transcriptional regulation was comparatively low. In contrast, atpT transcript stabilities differed dramatically, half-lives were 1.6min in the light, 33min in the dark and substantial changes were observed if glucose or DCMU were added. These findings show that transcriptional control of atpT involves nucleoid-associated DNA-binding proteins, positive regulation through RpaB, while the major effect on the condition-dependent regulation of atpT expression is mediated by controlling mRNA stability, which is related to the cellular redox and energy status. IMPORTANCE FoF1 ATP synthases produce ATP, the universal biological energy source. Under unfavorable conditions, ATP synthases can operate in a futile reverse reaction, pumping protons while ATP is used up. Cyanobacteria perform plant-like photosynthesis, but they cannot use the same mechanism as plant chloroplasts to inhibit ATP synthases during the night because respiratory and photosynthetic complexes are both located in the same membrane system. Atp Theta is a small protein encoded by the gene atpT in cyanobacteria that can prevent the ATP synthase reverse reaction (ATPase activity). Here we found that three transcription factors contribute to the regulation of atpT expression. However, the control of mRNA stability was identified as the major regulatory process governing atpT expression. Thus, it is the interplay between transcriptional and posttranscriptional regulation that position the Atp Theta -based regulatory mechanism within the context of the cellular redox and energy balance.
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页数:16
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