1994
DOI: 10.1128/jb.176.18.5622-5630.1994
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NADH dehydrogenase subunit genes in the mitochondrial DNA of yeasts

Abstract: The genes encoding the NADH dehydrogenase subunits of respiratory complex I have not been identified so far in the mitochondrial DNA (mtDNA) of yeasts. In the linear mtDNA of Candida parapsilosis, we found six new open reading frames whose sequences were unambiguously homologous to those of the genes known to code for NADH dehydrogenase subunit proteins of different organisms, i.e., ND1, ND2, ND3, ND4L, ND5, and ND6. The gene for ND4 also appears to be present, as judged from hybridization experiments with a P… Show more

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Cited by 72 publications
(51 citation statements)
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“…mtDNA was analyzed by pulsed-field gel electrophoresis (PFGE) essentially as described previously (59). Briefly, whole-cell DNA samples were prepared in agarose plugs containing Zymolyase 20T (final concentration, 0.5 mg/ml; Seikagaku Corp.) and were incubated overnight in solution I (10 mM Tris-HCl, 0.45 M EDTA-NaOH [pH 8.8], 7.5% [vol/vol] 2-mercaptoethanol) at 37°C.…”
Section: Microbialmentioning
confidence: 99%
“…mtDNA was analyzed by pulsed-field gel electrophoresis (PFGE) essentially as described previously (59). Briefly, whole-cell DNA samples were prepared in agarose plugs containing Zymolyase 20T (final concentration, 0.5 mg/ml; Seikagaku Corp.) and were incubated overnight in solution I (10 mM Tris-HCl, 0.45 M EDTA-NaOH [pH 8.8], 7.5% [vol/vol] 2-mercaptoethanol) at 37°C.…”
Section: Microbialmentioning
confidence: 99%
“…Pulsed Field Gel Electrophoresis-DNA samples were prepared as described previously (16). Briefly, yeast cells were lysed in agarose blocks by sequential treatment with zymolyase and proteinase K. Samples were electrophoretically separated in a 0.8% agarose gel in 0.5ϫ TBE (45 mM Tris borate, 1 mM EDTA) buffer in a Pulsaphor apparatus (LKB) in contour-clamped homogeneous electric field configuration.…”
Section: Preparation Of Mitochondrial Protein Extracts and Purificatimentioning
confidence: 99%
“…Next, the gene contents in both mtDNAs were inferred by sequencing the termini of the restriction fragments inserted within the plasmid vector. The data were then compared with the GenBank database as well as with the complete sequence of mtDNA of the group I strain CBS 7157 (Nosek & Fukuhara, 1994a Tomaska, unpublished). This approach led to the identification of nad1-5, cytb, atp6 and rrnL genes in MCO 456 and nad1-5, cytb, cox1, cox3, atp6 and rrnL in MCO 448.…”
Section: Physical Mapping Of Mtdna In Different Groups Of C Parapsilmentioning
confidence: 99%