Abstract

In Drosophila melanogaster, the mitochondrial transcription factor B1 (d-mtTFB1) transcript contains in its 5'-untranslated region a conserved upstream open reading frame denoted as CG42630 in FlyBase. We demonstrate that CG42630 encodes a novel protein, the coiled coil domain-containing protein 56 (CCDC56), conserved in metazoans. We show that Drosophila CCDC56 protein localizes to mitochondria and contains 87 amino acids in flies and 106 in humans with the two proteins sharing 42% amino acid identity. We show by rapid amplification of cDNA ends and Northern blotting that Drosophila CCDC56 protein and mtTFB1 are encoded on a bona fide bicistronic transcript. We report the generation and characterization of two ccdc56 knock-out lines in Drosophila carrying the ccdc56(D6) and ccdc56(D11) alleles. Lack of the CCDC56 protein in flies induces a developmental delay and 100% lethality by arrest of larval development at the third instar. ccdc56 knock-out larvae show a significant decrease in the level of fully assembled cytochrome c oxidase (COX) and in its activity, suggesting a defect in complex assembly; the activity of the other oxidative phosphorylation complexes remained either unaffected or increased in the ccdc56 knock-out larvae. The lethal phenotype and the decrease in COX were partially rescued by reintroduction of a wild-type UAS-ccdc56 transgene. These results indicate an important role for CCDC56 in the oxidative phosphorylation system and in particular in COX function required for proper development in D. melanogaster. We propose CCDC56 as a candidate factor required for COX biogenesis/assembly.

Highlights

  • Cytochrome c oxidase (COX), the final enzyme of the mitochondrial electron transport chain, requires several assembly factors for its proper function

  • The D. melanogaster Gene CG42630 Is Expressed in a Bicistronic mRNA with mitochondrial transcription factor B1 (mtTFB1) and Encodes a Novel Conserved Protein, coiled coil domain-containing protein 56 (CCDC56)—A search in the Drosophila genome database (FlyBase) indicated the existence of a upstream open reading frame (uORF) in the 5Ј-UTR of the mtTFB1 transcript located in the first exon of the mRNA (Fig. 1A)

  • We sequenced the cDNA clones obtained by 5Ј-Rapid amplification of cDNAs ends (RACE) from different Drosophila strains (w1118, n ϭ 8; Oregon R-C, n ϭ 6) and from cultured Schneider cells (n ϭ 6), and in all cases, sequence analyses detected a single transcript with a heterogeneous transcription start point located upstream from the CG42630 uORF (Fig. 1B)

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Summary

Background

Cytochrome c oxidase (COX), the final enzyme of the mitochondrial electron transport chain, requires several assembly factors for its proper function. Significance: Drosophila CCDC56 is a novel putative COX assembly factor conserved in humans. The lethal phenotype and the decrease in COX were partially rescued by reintroduction of a wild-type UAS-ccdc transgene These results indicate an important role for CCDC56 in the oxidative phosphorylation system and in particular in COX function required for proper development in D. melanogaster. The electron transport chain couples electron transfer from NADH and FADH2 to molecular oxygen with proton translocation from the matrix to the mitochondrial intermembrane space by complexes I, III, and IV. Our results indicate that the CCDC56 homolog is a mitochondrial protein required for COX activity and assembly in D. melanogaster, suggesting a role as a COX assembly factor

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