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J. Biol. Chem., Vol. 265, Issue 27, 16389-16393, 09, 1990
R Aggeler and RA Capaldi
The gene COX VII coding for yeast cytochrome c oxidase subunit VII has been
cloned by a two-step procedure. Two degenerate oligonucleotides
corresponding to amino- and carboxyl-terminal protein segments were used in
a polymerase chain reaction for the amplification of a major portion of
subunit VII (residues 1-52), which was then used for the cloning of
complete COX VII. From the nucleotide sequence, an additional
amino-terminal and two additional carboxyl-terminal amino acids are
predicted as compared with the described primary sequence (Power, S. D.,
Lochrie, M. A., and Poyton, R. O. (1986) J. Biol. Chem. 261, 9206-9209).
Beside subunit VIIa the subunit described here is the only nuclear encoded
subunit of cytochrome c oxidase in yeast without a leader sequence. COX VII
exists as a single copy per haploid genome as shown by Southern blot and
gene disruption. Null mutants produced by gene disruption at the COX VII
locus were respiratory-deficient. No cytochrome c oxidase activity was
detectable nor was there an assembly of the oxidase complex.
Yeast cytochrome c oxidase subunit VII is essential for assembly of an active enzyme. Cloning, sequencing, and characterization of the nuclear- encoded gene
Institute of Molecular Biology, University of Oregon, Eugene 97403.
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