Enzyme regulation. IRBIT is a novel regulator of ribonucleotide reductase in higher eukaryotes.

Article Details

Citation

Arnaoutov A, Dasso M

Enzyme regulation. IRBIT is a novel regulator of ribonucleotide reductase in higher eukaryotes.

Science. 2014 Sep 19;345(6203):1512-5. doi: 10.1126/science.1251550.

PubMed ID
25237103 [ View in PubMed
]
Abstract

Ribonucleotide reductase (RNR) supplies the balanced pools of deoxynucleotide triphosphates (dNTPs) necessary for DNA replication and maintenance of genomic integrity. RNR is subject to allosteric regulatory mechanisms in all eukaryotes, as well as to control by small protein inhibitors Sml1p and Spd1p in budding and fission yeast, respectively. Here, we show that the metazoan protein IRBIT forms a deoxyadenosine triphosphate (dATP)-dependent complex with RNR, which stabilizes dATP in the activity site of RNR and thus inhibits the enzyme. Formation of the RNR-IRBIT complex is regulated through phosphorylation of IRBIT, and ablation of IRBIT expression in HeLa cells causes imbalanced dNTP pools and altered cell cycle progression. We demonstrate a mechanism for RNR regulation in higher eukaryotes that acts by enhancing allosteric RNR inhibition by dATP.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Ribonucleoside-diphosphate reductase large subunitP23921Details