Summary:
NrdR is a zinc-finger/ATP cone transcriptional regulatory protein that regulates the expression of several operons that encode ribonucleotide reductases (RNRs), according to the abundance of deoxyribonucleoside triphosphates (dNTPs) generated from ribonucleotides [2, 3].
NrdR has an N-terminal zinc-finger-like DNA-binding domain and a C-terminal ATP cone domain. The ATP cone domain is similar to the allosteric domain found in some RNRs [1, 4] NrdR is bound by approximately equal amounts of ATP and dATP in vivo [3] Triphosphates bind preferentially to NrdR compared to nucleoside monophosphates and triphosphates [3] NrdR is directly regulated by ATP, rather than ATP serving as the cofactor to facilitate dATP binding [3]
The apo and holo forms of NrdR are capable of binding to DNA; furthermore, this binding capability is enhanced by high concentrations of zinc [5]
In Streptomyces coelicolor, it was shown that NrdR is an oligomeric protein that binds zinc, ATP, dATP, and the previously hypothesized NrdR box [6, 7].
In other bacteria, NrdR acts as a negative regulator of
nrd genes in
Mycobacterium spp.,
Chlamydia trachomatis, and
Salmonella enterica serovar Typhimurium (
[3] and references therein).
Mckethan and Spiro (2013) proposed a model in which NrdR selectively binds (deoxy)nucleoside triphosphates, which are hydrolyzed to their monophosphate counterparts in order to regulate DNA binding
[3] and those authors speculated that an as-yet-unidentified cellular event stimulates the conversion of NrdR-bound triphosphates to monophosphates, and that this is accompanied by an increase in DNA-binding affinity and downregulation of target genes
[3]
nrdR is expressed at similar levels during exponential- and stationary-phase growth and is not required for growth
[1].
The overexpression of NrdR affects bacterial growth, adhesion, flagella, and cell wall formation, resulting in irregular and smaller bacterial colony shapes, bacterial aggregates, and delays in the time to reach the exponential phase; it thereby acts as a negative regulator of bacterial growth
[5]
High temperatures affect the bacterial viability of a strain that overexpresses NrdR; however, an N-terminal deletion of this protein counteracted this effect. Furthermore, complementary overexpression of
polA,
thiL, or
eno also counteracted the effect caused by
nrdR overexpression
[5]
NrdR: "
nrd Regulation"
[2]
Review:
[8]
Read more >