7-deazaguanine has been researched along with queuine* in 2 studies
2 other study(ies) available for 7-deazaguanine and queuine
Article | Year |
---|---|
Queuine Analogues Incorporating the 7-Aminomethyl-7-deazaguanine Core: Structure-Activity Relationships in the Treatment of Experimental Autoimmune Encephalomyelitis.
A library of queuine analogues targeting the modification of tRNA isoacceptors for Asp, Asn, His and Tyr catalysed by queuine tRNA ribosyltransferase (QTRT, also known as TGT) was evaluated in the treatment of a chronic multiple sclerosis model: murine experimental autoimmune encephalomyelitis. Several active 7-deazaguanines emerged, together with a structure-activity relationship involving the necessity for a flexible alkyl chain of fixed length. Topics: Animals; Encephalomyelitis, Autoimmune, Experimental; Mice; Pentosyltransferases; RNA, Transfer; Structure-Activity Relationship | 2023 |
Queuine links translational control in eukaryotes to a micronutrient from bacteria.
In eukaryotes, the wobble position of tRNA with a GUN anticodon is modified to the 7-deaza-guanosine derivative queuosine (Q34), but the original source of Q is bacterial, since Q is synthesized by eubacteria and salvaged by eukaryotes for incorporation into tRNA. Q34 modification stimulates Dnmt2/Pmt1-dependent C38 methylation (m5C38) in the tRNAAsp anticodon loop in Schizosaccharomyces pombe. Here, we show by ribosome profiling in S. pombe that Q modification enhances the translational speed of the C-ending codons for aspartate (GAC) and histidine (CAC) and reduces that of U-ending codons for asparagine (AAU) and tyrosine (UAU), thus equilibrating the genome-wide translation of synonymous Q codons. Furthermore, Q prevents translation errors by suppressing second-position misreading of the glycine codon GGC, but not of wobble misreading. The absence of Q causes reduced translation of mRNAs involved in mitochondrial functions, and accordingly, lack of Q modification causes a mitochondrial defect in S. pombe. We also show that Q-dependent stimulation of Dnmt2 is conserved in mice. Our findings reveal a direct mechanism for the regulation of translational speed and fidelity in eukaryotes by a nutrient originating from bacteria. Topics: Animals; Anticodon; Asparagine; DNA (Cytosine-5-)-Methyltransferases; DNA, Mitochondrial; Eukaryota; Guanine; Methylation; Mice; Micronutrients; Protein Biosynthesis; Ribosomes; RNA, Transfer; Schizosaccharomyces; Schizosaccharomyces pombe Proteins; Tyrosine | 2019 |