Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:1.9.3.1 (
cytochrome oxidase
)
8,822
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The Arabidopsis
HCC1
gene is a homologue of the copper chaperone SCO1 from the yeast Saccharomyces cerevisiae. SCO1 (synthesis of cytochrome c oxidase 1) encodes a mitochondrial protein that is essential for the correct assembly of
complex IV
in the respiratory chain. GUS analyses showed
HCC1
promoter activity in vascular tissue, guard cells, hydathodes, trichome support cells, and embryos.
HCC1
function was studied in two hcc1 T-DNA insertion lines, hcc1-1 and hcc1-2. Gametophyte development was not affected by the disruption of
HCC1
, but homozygous hcc1-1 and hcc1-2 embryos became arrested at various developmental stages, mostly at the heart stage. Both the wild-type
HCC1
gene and the modified gene coding for the C-terminally SNAP-tagged
HCC1
were able to complement the embryo-lethal phenotype of the hcc1-1 line. Localization of the SNAP-tagged
HCC1
in transgenic lines identified
HCC1
as a mitochondrial protein. To determine if
HCC1
is a functional homologue to Sco1p, the respiratory-deficient yeast sco1 mutant was transformed with chimeric constructs containing different combinations of
HCC1
and SCO1 sequences. One of the resulting chimeric proteins restored respiration in the yeast mutant. This protein had the N-terminal mitochondrial targeting signal and the single transmembrane domain derived from Sco1p and the C-terminal half (including the copper-binding motif) derived from
HCC1
. Growth of the complemented yeast mutant was enhanced by the addition of copper to the medium. The data demonstrate that
HCC1
is essential for embryo development in Arabidopsis, possibly due to its role in cytochrome c oxidase assembly.
...
PMID:HCC1, the Arabidopsis homologue of the yeast mitochondrial copper chaperone SCO1, is essential for embryonic development. 2104 73