COQ7
{{Short description|Protein-coding gene in humans}}
{{Redirect|clk-1|other uses|CLK-1 (disambiguation)}}
{{Infobox_gene}}
Mitochondrial 5-demethoxyubiquinone hydroxylase (DMQ hydroxylase), also known as coenzyme Q7, hydroxylase, is an enzyme that in humans is encoded by the COQ7 gene. The clk-1 (clock-1) gene encodes this protein that is necessary for ubiquinone biosynthesis in the worm Caenorhabditis elegans and other eukaryotes. The mouse version of the gene is called mclk-1 and the human, fruit fly and yeast homolog COQ7 (coenzyme Q biosynthesis protein 7).{{cite web | title = Entrez Gene: COQ7 coenzyme Q7 homolog, ubiquinone (yeast)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10229}}
CLK-1 is not to be confused with the unrelated human protein CLK1 which plays a role in RNA splicing.
Structure
The protein has two repeats of approximately 90 amino acids, that contain two conserved motifs predicted to be important for coordination of iron. The structure and function of the gene are highly conserved among different species.{{cite journal | vauthors = Liu X, Jiang N, Hughes B, Bigras E, Shoubridge E, Hekimi S | title = Evolutionary conservation of the clk-1-dependent mechanism of longevity: loss of mclk1 increases cellular fitness and lifespan in mice | journal = Genes Dev. | volume = 19 | issue = 20 | pages = 2424–34 |date=October 2005 | pmid = 16195414 | pmc = 1257397 | doi = 10.1101/gad.1352905 }}
The C. elegans protein contains 187 amino acid residues (20 kilodaltons), the human homolog 217 amino acid residues (24 kilodaltons, gene consisting of six exons spanning 11 kb and located on chromosome 16).{{cite journal | vauthors = Asaumi S, Kuroyanagi H, Seki N, Shirasawa T | title = Orthologues of the Caenorhabditis elegans longevity gene clk-1 in mouse and human | journal = Genomics | volume = 58 | issue = 3 | pages = 293–301 |date=June 1999 | pmid = 10373327 | doi = 10.1006/geno.1999.5838 }}
Mitochondrial function
Ubiquinone is a small redox active lipid that is found in most cellular membranes where it acts as a cofactor in numerous cellular redox processes, including mitochondrial electron transport. As a cofactor, ubiquinone is often involved in processes that produce reactive oxygen species (ROS). In addition, ubiquinone is one of the main endogenous antioxidants of the cell. The CLK-1 enzyme is responsible for the hydroxylation of 5-demethoxyubiquinone to 5-hydroxyubiquinone.
It has been shown that mutations in the gene are associated with increased lifespan.{{cite journal | vauthors = Ewbank JJ, Barnes TM, Lakowski B, Lussier M, Bussey H, Hekimi S | title = Structural and functional conservation of the Caenorhabditis elegans timing gene clk-1 | journal = Science | volume = 275 | issue = 5302 | pages = 980–3 |date=February 1997 | pmid = 9020081 | doi = 10.1126/science.275.5302.980 | s2cid = 32191959 }} Defects of the gene slow down a variety of developmental and physiological processes, including the cell cycle, embryogenesis, post-embryonic growth, rhythmic behaviors and aging.{{cite journal | vauthors = Felkai S, Ewbank JJ, Lemieux J, Labbé JC, Brown GG, Hekimi S | title = CLK-1 controls respiration, behavior and aging in the nematode Caenorhabditis elegans | journal = EMBO J. | volume = 18 | issue = 7 | pages = 1783–92 |date=April 1999 | pmid = 10202142 | pmc = 1171264 | doi = 10.1093/emboj/18.7.1783 }}
Nuclear function
CLK-1 and COQ7 predominantly localise to mitochondria to participate in the ubiquinone biosynthetic pathway which is found there. However, a small pool of CLK-1 and COQ7 translocates to the nucleus in response to the production of ROS by normally functioning mitochondria in both worms and human cells, respectively.{{cite journal | vauthors = Monaghan RM, Barnes RG, Fisher K, Andreou T, Rooney N, Poulin GB, Whitmarsh AJ | title = A nuclear role for the respiratory enzyme CLK-1 in regulating mitochondrial stress responses and longevity | journal = Nature Cell Biology |date=June 2015 | pmid = 25961505 | doi = 10.1038/ncb3170 | volume=17 | issue = 6 | pages=782–92 | pmc=4539581}} Translocation of CLK-1 and COQ7 represents a mitochondrial to nuclear retrograde signalling pathway that acts to suppress mitochondrial stress responses. The mitochondrial and nuclear pools of CLK-1 are thought to contribute independently to worm lifespan regulation. The nuclear form of CLK-1 and COQ7 is thought to regulate gene expression through an unidentified mechanism.
References
{{Reflist}}
Further reading
{{refbegin | 2}}
- {{cite journal | vauthors=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1–2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }}
- {{cite journal | vauthors=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1–2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 |display-authors=etal}}
- {{cite journal | vauthors=Jonassen T, Proft M, Randez-Gil F |title=Yeast Clk-1 homologue (Coq7/Cat5) is a mitochondrial protein in coenzyme Q synthesis. |journal=J. Biol. Chem. |volume=273 |issue= 6 |pages= 3351–7 |year= 1998 |pmid= 9452453 |doi=10.1074/jbc.273.6.3351 |display-authors=etal|doi-access=free }}
- {{cite journal | vauthors=Asaumi S, Kuroyanagi H, Seki N, Shirasawa T |title=Orthologues of the Caenorhabditis elegans longevity gene clk-1 in mouse and human. |journal=Genomics |volume=58 |issue= 3 |pages= 293–301 |year= 1999 |pmid= 10373327 |doi= 10.1006/geno.1999.5838 }}
- {{cite journal | vauthors=Vajo Z, King LM, Jonassen T |title=Conservation of the Caenorhabditis elegans timing gene clk-1 from yeast to human: a gene required for ubiquinone biosynthesis with potential implications for aging. |journal=Mamm. Genome |volume=10 |issue= 10 |pages= 1000–4 |year= 2000 |pmid= 10501970 |doi=10.1007/s003359901147 |s2cid=13800512 |display-authors=etal}}
- {{cite journal | vauthors=Hartley JL, Temple GF, Brasch MA |title=DNA cloning using in vitro site-specific recombination. |journal=Genome Res. |volume=10 |issue= 11 |pages= 1788–95 |year= 2001 |pmid= 11076863 |doi=10.1101/gr.143000 | pmc=310948 }}
- {{cite journal | vauthors=Wiemann S, Weil B, Wellenreuther R |title=Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. |journal=Genome Res. |volume=11 |issue= 3 |pages= 422–35 |year= 2001 |pmid= 11230166 |doi= 10.1101/gr.GR1547R | pmc=311072 |display-authors=etal}}
- {{cite journal | vauthors=Simpson JC, Wellenreuther R, Poustka A |title=Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. |journal=EMBO Rep. |volume=1 |issue= 3 |pages= 287–92 |year= 2001 |pmid= 11256614 |doi= 10.1093/embo-reports/kvd058 | pmc=1083732 |display-authors=etal}}
- {{cite journal | vauthors=Stenmark P, Grünler J, Mattsson J |title=A new member of the family of di-iron carboxylate proteins. Coq7 (clk-1), a membrane-bound hydroxylase involved in ubiquinone biosynthesis. |journal=J. Biol. Chem. |volume=276 |issue= 36 |pages= 33297–300 |year= 2001 |pmid= 11435415 |doi= 10.1074/jbc.C100346200 |display-authors=etal|doi-access=free }}
- {{cite journal | vauthors=Takahashi M, Asaumi S, Honda S |title=Mouse coq7/clk-1 orthologue rescued slowed rhythmic behavior and extended life span of clk-1 longevity mutant in Caenorhabditis elegans. |journal=Biochem. Biophys. Res. Commun. |volume=286 |issue= 3 |pages= 534–40 |year= 2001 |pmid= 11511092 |doi= 10.1006/bbrc.2001.5439 |display-authors=etal}}
- {{cite journal | author=Rea S |title=CLK-1/Coq7p is a DMQ mono-oxygenase and a new member of the di-iron carboxylate protein family. |journal=FEBS Lett. |volume=509 |issue= 3 |pages= 389–94 |year= 2002 |pmid= 11749961 |doi=10.1016/S0014-5793(01)03099-X |s2cid=28650687 |doi-access=free }}
- {{cite journal | vauthors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |bibcode=2002PNAS...9916899M |display-authors=etal|doi-access=free }}
- {{cite journal | vauthors=Ota T, Suzuki Y, Nishikawa T |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |display-authors=etal|doi-access=free }}
- {{cite journal | vauthors=Wiemann S, Arlt D, Huber W |title=From ORFeome to biology: a functional genomics pipeline. |journal=Genome Res. |volume=14 |issue= 10B |pages= 2136–44 |year= 2004 |pmid= 15489336 |doi= 10.1101/gr.2576704 | pmc=528930 |display-authors=etal}}
- {{cite journal | vauthors=Mehrle A, Rosenfelder H, Schupp I |title=The LIFEdb database in 2006. |journal=Nucleic Acids Res. |volume=34 |issue= Database issue |pages= D415–8 |year= 2006 |pmid= 16381901 |doi= 10.1093/nar/gkj139 | pmc=1347501 |display-authors=etal}}
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External links
{{Portal|Biology}}
- {{UCSC genome browser|COQ7}}
- {{UCSC gene details|COQ7}}
{{Monooxygenases}}
{{Enzymes}}
{{gene-16-stub}}