Breuer Ruth, Gomes-Filho José Vicente, Yuan Jing, Randau Lennart
Prokaryotic RNA Biology, Department of Biology, Philipps-Universität Marburg, Marburg, Germany.
Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Front Microbiol. 2023 Jun 15;14:1197877. doi: 10.3389/fmicb.2023.1197877. eCollection 2023.
Nudix hydrolases comprise a large and ubiquitous protein superfamily that catalyzes the hydrolysis of a nucleoside diphosphate linked to another moiety X (Nudix). possesses four Nudix domain-containing proteins (SACI_RS00730/Saci_0153, SACI_RS02625/Saci_0550, SACI_RS00060/Saci_0013/Saci_NudT5, and SACI_RS00575/Saci_0121). Deletion strains were generated for the four individual Nudix genes and for both Nudix genes annotated to encode ADP-ribose pyrophosphatases () and did not reveal a distinct phenotype compared to the wild-type strain under standard growth conditions, nutrient stress or heat stress conditions. We employed RNA-seq to establish the transcriptome profiles of the Nudix deletion strains, revealing a large number of differentially regulated genes, most notably in the Δ double knock-out strain and the Δ single deletion strain. The absence of Nudix hydrolases is suggested to impact transcription differentially regulated transcriptional regulators. We observed downregulation of the lysine biosynthesis and the archaellum formation iModulons in stationary phase cells, as well as upregulation of two genes involved in the NAD biosynthesis pathway. Furthermore, the deletion strains exhibited upregulation of two thermosome subunits (α, β) and the toxin-antitoxin system VapBC, which are implicated in the archaeal heat shock response. These results uncover a defined set of pathways that involve archaeal Nudix protein activities and assist in their functional characterization.
Nudix水解酶构成了一个庞大且普遍存在的蛋白质超家族,该家族催化与另一个部分X(Nudix)相连的核苷二磷酸的水解。[该生物]拥有四种含Nudix结构域的蛋白质(SACI_RS00730/Saci_0153、SACI_RS02625/Saci_0550、SACI_RS00060/Saci_0013/Saci_NudT5和SACI_RS00575/Saci_0121)。针对四个单独的Nudix基因以及注释为编码ADP - 核糖焦磷酸酶的两个Nudix基因构建了缺失菌株,但在标准生长条件、营养胁迫或热胁迫条件下,与野生型菌株相比,并未显示出明显的表型差异。我们采用RNA测序来建立Nudix缺失菌株的转录组图谱,揭示了大量差异调节基因,最显著的是在Δ双敲除菌株和Δ单缺失菌株中。Nudix水解酶的缺失被认为会影响转录,从而导致差异调节的转录调节因子。我们观察到在稳定期细胞中赖氨酸生物合成和古菌鞭毛形成iModulons的下调,以及参与NAD生物合成途径的两个基因的上调。此外,缺失菌株表现出两个热体亚基(α、β)和毒素 - 抗毒素系统VapBC的上调,这与古菌热休克反应有关。这些结果揭示了一组明确的涉及古菌Nudix蛋白活性的途径,并有助于对其进行功能表征。