ライフサイエンスコーパス: tRNA(Ile)

1 activated valine from being stably joined to tRNAIle.

2 ady-state levels of the mature mitochondrial tRNA(Ile).

3 f a small group I ribozyme from Azoarcus pre-tRNA(ile).

4 more efficiently than 5'-extended precursor tRNA(Ile).

5 us been identified: tRNA(Asp), tRNA(Ala) and tRNA(Ile).

6 ylate synthesis but no detectable binding to tRNA(Ile).

7 ied a pathogenic, heteroplasmic mitochondria tRNA(Ile) (4274T>C) mutation.

8 Here we show that tRNA(Ile) affects both the synthetic and editing reactio

9 noacyl-tRNA synthetases, IleRS can mischarge tRNA(Ile) and correct this misacylation through a separa

10 f Staphylococcus aureus IleRS complexed with tRNA(Ile) and Mupirocin shows the acceptor strand of the

11 valyl-tRNA synthetase (ValRS) deacylate Val-tRNA(Ile) and Thr-tRNA(Val), respectively.

12 demonstrated specific binding to the cognate tRNA(Ile) and tRNA(Ile)-dependent structural rearrangeme

13 A(Gln) was mainly cytosolic in localization; tRNA(Ile) and tRNA(Lys) were mainly mitochondrial; and t

14 omprised of just the acceptor-TPsiC helix of tRNAIle are substrates for specific aminoacylation by Il

15 n human mitochondrial isoleucine tRNA (hs mt tRNA(Ile)) are associated with cardiomyopathy and opthal

16 r RNA (tRNA) synthetase (IleRS) joins Ile to tRNA(Ile) at its synthetic active site and hydrolyzes in

17 es valine (to produce valyl adenylate or Val-tRNA(Ile)) at its active site.

18 t-tRNA(Leu(UUR)) or with mutations in the mt-tRNA(Ile), both of which are aminoacylated by Class I mt

19 pecific binding to the cognate tRNA(Ile) and tRNA(Ile)-dependent structural rearrangements consistent

20 eRS.Ile-AMP and IleRS.Ile-tRNAIle, IleRS.Val-tRNAIle does not react with thiols.

21 The conformation of a group I pre-tRNA(ile) from the bacterium Azoarcus was probed by ribo

22 ned a tRNA(Ala) gene, while ISR2 contained a tRNA(Ile) gene.

23 Our data indicate that tRNA(Ile) identity elements were established late and in

24 fficiently as do IleRS.Ile-AMP and IleRS.Ile-tRNAIle, IleRS.Val-tRNAIle does not react with thiols.

25 d Mupirocin shows the acceptor strand of the tRNA(Ile) in the continuously stacked, A-form conformati

26 ize, the 205 nt group I intron from Azoarcus tRNA(Ile) is an exceptionally stable self-splicing RNA.

27 n RNA hairpin that mimics the D-stem/loop of tRNAIle is also unable to induce the hydrolysis of misac

28 Thus, the native tertiary fold of tRNAIle is required to promote efficient editing.

29 t the mischarged valine residue in IleRS.Val-tRNAIle is, most likely, positioned off the enzyme.

30 biguity exists in the recognition of certain tRNA(Ile) isoacceptors that are initially transcribed wi

31 encoding tRNA(Gln), the control region, and tRNA(Ile) located downstream of the two ribosomal RNA ge

32 solated in which the essential gene encoding tRNA(Ile)-lysidine synthetase was deleted for the first

33 so be a determinant for the essential enzyme tRNA(Ile)-lysidine synthetase.

34 s during the mechanistic characterization of tRNA(Ile)-lysidine synthetase.

35 endent formation of lysidine is catalyzed by tRNA(Ile)-lysidine synthetase.

36 Here we show that, in contrast to tRNAIle, minihelixIle is unable to trigger the hydrolysi

37 33P) mutant of Bacillus subtilis that allows tRNA(Ile) mischarging while retaining wild-type Ile-tRNA

38 Finally, the extent to which tRNA(Ile) modulates activation and pre-transfer editing

39 its probable occurrence in the AUA decoding tRNA(Ile) of euryarchaea and crenarchaea.

40 ces comprised of the acceptor-TpsiC helix of tRNA(Ile) or tRNA(Val) were aminoacylated by cognate syn

41 these enzymatic reactions occur between Ile-tRNAIle or Ile-AMP (bound in the synthetic sub-site) and

42 However, the molecular mechanisms by which tRNA(Ile) organizes the synthetic site to enhance pre-tr

43 organisms, the C34 wobble position in these tRNA(Ile) precursors is rapidly modified to lysidine to

44 PCR amplification of the 16S-tRNA(Ile) region of ISR2 permitted rapid phylotyping of

45 he actual distribution of lysidine-dependent tRNA(Ile) rejection by MRS, we have investigated the abi

46 of a small group I intron from Azoarcus pre-tRNA(Ile) showed that tertiary interactions between heli

47 e) mischarging while retaining wild-type Ile-tRNA(Ile) synthesis activity.

48 or-prone and kinetically optimized isoleucyl-tRNA(Ile) synthesis under cellular conditions.

49 etase (MRS) and production of a chimeric Met-tRNA(Ile) that would compromise translational fidelity.

50 first anticodon position of the AUA decoding tRNA(Ile) (tRNA2(Ile)) of bacteria and archaea is essent

51 5'- and 3'-end maturation of tRNA(Trp)(CCA), tRNA(Ile)(UAU), tRNA(Gln)(CUG), tRNA(Lys)(UUU), and tRNA

52 fl-tRNA(Ile)UAU-generated FRET signals were specifically en

53 stent with this model, T7-transcribed mature tRNA(Ile) underwent importation in vitro into isolated m

54 ing group-I intron interrupting the Azoarcus tRNA(Ile) was shortened by ~10% with the removal of heli

55 ing reaction is dependent on the presence of tRNAIle, which contains discrete D-loop nucleotides that

56 whose essential function is to aminoacylate tRNA(Ile) with isoleucine.