Rodionov Dmitry A, De Ingeniis Jessica, Mancini Chiara, Cimadamore Flavio, Zhang Hong, Osterman Andrei L, Raffaelli Nadia
Burnham Institute for Medical Research, La Jolla, CA 92037, USA.
Nucleic Acids Res. 2008 Apr;36(6):2047-59. doi: 10.1093/nar/gkn047. Epub 2008 Feb 14.
A novel family of transcription factors responsible for regulation of various aspects of NAD synthesis in a broad range of bacteria was identified by comparative genomics approach. Regulators of this family (here termed NrtR for Nudix-related transcriptional regulators), currently annotated as ADP-ribose pyrophosphatases from the Nudix family, are composed of an N-terminal Nudix-like effector domain and a C-terminal DNA-binding HTH-like domain. NrtR regulons were reconstructed in diverse bacterial genomes by identification and comparative analysis of NrtR-binding sites upstream of genes involved in NAD biosynthetic pathways. The candidate NrtR-binding DNA motifs showed significant variability between microbial lineages, although the common consensus sequence could be traced for most of them. Bioinformatics predictions were experimentally validated by gel mobility shift assays for two NrtR family representatives. ADP-ribose, the product of glycohydrolytic cleavage of NAD, was found to suppress the in vitro binding of NrtR proteins to their DNA target sites. In addition to a major role in the direct regulation of NAD homeostasis, some members of NrtR family appear to have been recruited for the regulation of other metabolic pathways, including sugar pentoses utilization and biogenesis of phosphoribosyl pyrophosphate. This work and the accompanying study of NiaR regulon demonstrate significant variability of regulatory strategies for control of NAD metabolic pathway in bacteria.
通过比较基因组学方法,在多种细菌中鉴定出了一个负责调控NAD合成各个方面的新型转录因子家族。该家族的调控因子(此处称为NrtR,即与Nudix相关的转录调控因子)目前被注释为来自Nudix家族的ADP核糖焦磷酸酶,由一个N端的Nudix样效应结构域和一个C端的DNA结合HTH样结构域组成。通过对参与NAD生物合成途径的基因上游NrtR结合位点的鉴定和比较分析,在不同细菌基因组中重建了NrtR调控子。尽管大多数候选NrtR结合DNA基序的共同共有序列可以追溯,但微生物谱系之间的候选NrtR结合DNA基序存在显著差异。通过凝胶迁移率变动分析对两个NrtR家族代表进行了实验验证,证实了生物信息学预测。NAD糖水解裂解产物ADP核糖被发现可抑制NrtR蛋白与其DNA靶位点的体外结合。除了在直接调控NAD稳态中起主要作用外,NrtR家族的一些成员似乎还被招募用于调控其他代谢途径,包括戊糖利用和磷酸核糖焦磷酸的生物合成。这项工作以及对NiaR调控子的相关研究表明,细菌中NAD代谢途径的调控策略存在显著差异。