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. 2008 Nov 11;66(1):173. doi: 10.1007/s00018-008-8547-7

Hydroxylation of demethoxy-Q6 constitutes a control point in yeast coenzyme Q6 biosynthesis

S Padilla 1, U C Tran 2, M Jiménez-Hidalgo 1, J M López-Martín 1, A Martín-Montalvo 1, C F Clarke 2, P Navas 1, C Santos-Ocaña 1,
PMCID: PMC3070445  NIHMSID: NIHMS276730  PMID: 19002377

Abstract.

Coenzyme Q is a lipid molecule required for respiration and antioxidant protection. Q biosynthesis in Saccharomyces cerevisiae requires nine proteins (Coq1p–Coq9p). We demonstrate in this study that Q levels are modulated during growth by its conversion from demethoxy-Q (DMQ), a late intermediate. Similar conversion was produced when cells were subjected to oxidative stress conditions. Changes in Q6/DMQ6 ratio were accompanied by changes in COQ7 gene mRNA levels encoding the protein responsible for the DMQ hydroxylation, the penultimate step in Q biosynthesis pathway. Yeast coq null mutant failed to accumulate any Q late biosynthetic intermediate. However, in coq7 mutants the addition of exogenous Q produces the DMQ synthesis. Similar effect was produced by over-expressing ABC1/COQ8. These results support the existence of a biosynthetic complex that allows the DMQ6 accumulation and suggest that Coq7p is a control point for the Q biosynthesis regulation in yeast.

Electronic supplementary material

The online version of this article (doi:10.1007/s00018-008-8547-7) contains supplementary material, which is available to authorized users.

Keywords. Ubiquinone, coenzyme Q, mitochondria, yeast regulation

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Footnotes

Received 04 September 2008; received after revision 22 October 2008; accepted 23 October 2008

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Supplementary Materials

ESM (PDF 460 kb) (459.9KB, pdf)

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