Rescue of Yeast Defective in Mitochondrial ATP Synthase Subunit 8 by a Heterologous Gene from Aspergillus nidulans

Mitochondrial ATP synthase subunit 8 of the yeast Saccharomyces cerevisiae and of the filamentous fungus Aspergillus nidulans have the same length and similar structural motifs. However, the two proteins share only 50% identical residues, with the conserved residues being concentrated in the N- and...

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Veröffentlicht in:Biochemical and biophysical research communications 1994-09, Vol.203 (3), p.1567-1573
Hauptverfasser: Straffon, A.F.L., Nagley, P., Devenish, R.J.
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Sprache:eng
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Zusammenfassung:Mitochondrial ATP synthase subunit 8 of the yeast Saccharomyces cerevisiae and of the filamentous fungus Aspergillus nidulans have the same length and similar structural motifs. However, the two proteins share only 50% identical residues, with the conserved residues being concentrated in the N- and C-terminal domains. We have investigated whether it is amino acid sequence or overall structural motifs that are required for subunit and function. PCR was used to construct a gene encoding A. nidulans subunit 8 fused to an N-terminal cleavable mitochondrial targeting sequence. Following expression in the nucleus of a yeast strain deficient in subunit 8, the chimaeric precursor targeted the subunit 8 protein back to the mitochondrion. The A. nidulans subunit 8 was found to be able to restore growth on non-fermentable substrate at 18°C and 28°C, but not at 36°C. Given the sequence divergence between subunit 8 of A. nidulans and that of S. cerevisiae, this finding suggests that common structural motifs are important for subunit 8 function.
ISSN:0006-291X
1090-2104
DOI:10.1006/bbrc.1994.2365