| Literature DB >> 23933583 |
Natalie Al-Furoukh1, Steffi Goffart2, Marten Szibor3, Sjoerd Wanrooij4, Thomas Braun5.
Abstract
NOA1 is an evolutionary conserved, nuclear encoded GTPase essential for mitochondrial function and cellular survival. The function of NOA1 for assembly of mitochondrial ribosomes and regulation of OXPHOS activity depends on its GTPase activity, but so far no ligands have been identified that regulate the GTPase activity of NOA1. To identify nucleic acids that bind to the RNA-binding domain of NOA1 we employed SELEX (Systemic Evolution of Ligands by EXponential Enrichment) using recombinant mouse wildtype NOA1 and the GTPase mutant NOA1-K353R. We found that NOA1 binds specifically to oligonucleotides that fold into guanine tetrads (G-quadruplexes). Binding of G-quadruplex oligonucleotides stimulated the GTPase activity of NOA1 suggesting a regulatory link between G-quadruplex containing RNAs, NOA1 function and assembly of mitochondrial ribosomes.Entities:
Keywords: Aptamer; Binding motif; G-quadruplex; GTPase; NOA1; Nitric Oxide Associated 1; OXPHOS; SELEX; Systemic Evolution of Ligands by Exponential Enrichment; UTR; double stranded; ds; oxidative phosphorylation; single stranded; ss; untranslated region
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Year: 2013 PMID: 23933583 DOI: 10.1016/j.bbamcr.2013.07.022
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002