137 related articles for article (PubMed ID: 26780366)
1. Partial suppression of the respiratory defect of qrs1/her2 glutamyl-tRNA amidotransferase mutants by overexpression of the mitochondrial pentatricopeptide Msc6p.
Moda BS; Ferreira-Júnior JR; Barros MH
Curr Genet; 2016 Aug; 62(3):607-17. PubMed ID: 26780366
[TBL] [Abstract][Full Text] [Related]
2. Her2p molecular modeling, mutant analysis and intramitochondrial localization.
Ferreira-Júnior JR; Bleicher L; Barros MH
Fungal Genet Biol; 2013 Nov; 60():133-9. PubMed ID: 23850602
[TBL] [Abstract][Full Text] [Related]
3. Msc6p is required for mitochondrial translation initiation in the absence of formylated Met-tRNA
Franco LVR; Moda BS; Soares MAKM; Barros MH
FEBS J; 2019 Apr; 286(7):1407-1419. PubMed ID: 30767393
[TBL] [Abstract][Full Text] [Related]
4. Characterization of Gtf1p, the connector subunit of yeast mitochondrial tRNA-dependent amidotransferase.
Barros MH; Rak M; Paulela JA; Tzagoloff A
J Biol Chem; 2011 Sep; 286(38):32937-47. PubMed ID: 21799017
[TBL] [Abstract][Full Text] [Related]
5. Analyzing the suppression of respiratory defects in the yeast model of human mitochondrial tRNA diseases.
Montanari A; Zhou YF; D'Orsi MF; Bolotin-Fukuhara M; Frontali L; Francisci S
Gene; 2013 Sep; 527(1):1-9. PubMed ID: 23727608
[TBL] [Abstract][Full Text] [Related]
6. Saccharomyces cerevisiae imports the cytosolic pathway for Gln-tRNA synthesis into the mitochondrion.
Rinehart J; Krett B; Rubio MA; Alfonzo JD; Söll D
Genes Dev; 2005 Mar; 19(5):583-92. PubMed ID: 15706032
[TBL] [Abstract][Full Text] [Related]
7. Yeast mitochondrial Gln-tRNA(Gln) is generated by a GatFAB-mediated transamidation pathway involving Arc1p-controlled subcellular sorting of cytosolic GluRS.
Frechin M; Senger B; Brayé M; Kern D; Martin RP; Becker HD
Genes Dev; 2009 May; 23(9):1119-30. PubMed ID: 19417106
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial cysteinyl-tRNA synthetase is expressed via alternative transcriptional initiation regulated by energy metabolism in yeast cells.
Nishimura A; Nasuno R; Yoshikawa Y; Jung M; Ida T; Matsunaga T; Morita M; Takagi H; Motohashi H; Akaike T
J Biol Chem; 2019 Sep; 294(37):13781-13788. PubMed ID: 31350340
[TBL] [Abstract][Full Text] [Related]
9. Recent Advances in Mitochondrial Aminoacyl-tRNA Synthetases and Disease.
Sissler M; González-Serrano LE; Westhof E
Trends Mol Med; 2017 Aug; 23(8):693-708. PubMed ID: 28716624
[TBL] [Abstract][Full Text] [Related]
10. Idiosyncrasies in decoding mitochondrial genomes.
Huot JL; Enkler L; Megel C; Karim L; Laporte D; Becker HD; Duchêne AM; Sissler M; Maréchal-Drouard L
Biochimie; 2014 May; 100():95-106. PubMed ID: 24440477
[TBL] [Abstract][Full Text] [Related]
11. Mitochondrial diseases: Yeast as a model for the study of suppressors.
Francisci S; Montanari A
Biochim Biophys Acta Mol Cell Res; 2017 Apr; 1864(4):666-673. PubMed ID: 28089773
[TBL] [Abstract][Full Text] [Related]
12. Human mitochondrial tRNA quality control in health and disease: a channelling mechanism?
Belostotsky R; Frishberg Y; Entelis N
RNA Biol; 2012 Jan; 9(1):33-9. PubMed ID: 22258151
[TBL] [Abstract][Full Text] [Related]
13. Cytonuclear Interactions in the Evolution of Animal Mitochondrial tRNA Metabolism.
Pett W; Lavrov DV
Genome Biol Evol; 2015 Jun; 7(8):2089-101. PubMed ID: 26116918
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial tRNA import and its consequences for mitochondrial translation.
Schneider A
Annu Rev Biochem; 2011; 80():1033-53. PubMed ID: 21417719
[TBL] [Abstract][Full Text] [Related]
15. The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.
Sasarman F; Antonicka H; Shoubridge EA
Hum Mol Genet; 2008 Dec; 17(23):3697-707. PubMed ID: 18753147
[TBL] [Abstract][Full Text] [Related]
16. Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy.
Scheidecker S; Bär S; Stoetzel C; Geoffroy V; Lannes B; Rinaldi B; Fischer F; Becker HD; Pelletier V; Pagan C; Acquaviva-Bourdain C; Kremer S; Mirande M; Tranchant C; Muller J; Friant S; Dollfus H
Hum Mutat; 2019 Oct; 40(10):1826-1840. PubMed ID: 31116475
[TBL] [Abstract][Full Text] [Related]
17. Three genes for mitochondrial proteins suppress null-mutations in both Afg3 and Rca1 when over-expressed.
Rep M; Nooy J; Guélin E; Grivell LA
Curr Genet; 1996 Aug; 30(3):206-11. PubMed ID: 8753648
[TBL] [Abstract][Full Text] [Related]
18. Rmd9p controls the processing/stability of mitochondrial mRNAs and its overexpression compensates for a partial deficiency of oxa1p in Saccharomyces cerevisiae.
Nouet C; Bourens M; Hlavacek O; Marsy S; Lemaire C; Dujardin G
Genetics; 2007 Mar; 175(3):1105-15. PubMed ID: 17194787
[TBL] [Abstract][Full Text] [Related]
19. The transcriptional activator HAP4 is a high copy suppressor of an oxa1 yeast mutation.
Hlavacek O; Bourens M; Salone V; Lachacinski N; Lemaire C; Dujardin G
Gene; 2005 Jul; 354():53-7. PubMed ID: 15908145
[TBL] [Abstract][Full Text] [Related]
20. Does the study of genetic interactions help predict the function of mitochondrial proteins in Saccharomyces cerevisiae?
Ostojić J; Glatigny A; Herbert CJ; Dujardin G; Bonnefoy N
Biochimie; 2014 May; 100():27-37. PubMed ID: 24262604
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]