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词条 COX4I2
释义

  1. Structure

  2. Function

  3. Clinical Significance

  4. Interactions

  5. References

  6. External links

  7. Further reading

{{Infobox_gene}}Cytochrome c oxidase subunit 4 isoform 2, mitochondrial is an enzyme that in humans is encoded by the COX4I2 gene.[1][2] COX4I2 is a nuclear-encoded isoform of cytochrome c oxidase (COX) subunit 4. Cytochrome c oxidase (complex IV) is a multi-subunit enzyme complex that couples the transfer of electrons from cytochrome c to molecular oxygen and contributes to a proton electrochemical gradient across the inner mitochondrial membrane, acting as the terminal enzyme of the mitochondrial respiratory chain. Mutations in COX4I2 have been associated with exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis (EPIDACH).[3][4]

Structure

COX4I2 is located on the q arm of chromosome 20 in position 11.21 and has 6 exons.[3] The COX4I2 gene produces a 20 kDa protein composed of 171 amino acids.[5][6] The protein encoded by COX4I2 belongs to the cytochrome c oxidase IV family. COX4I2 has a transit peptide domain and a disulfide bond amino acid modification.[7][8] A Glu138 residue, which corresponds to a Glu136 residue in COX4I1, is believed to be highly conserved and structurally important for the mitochondrial COX response to hypoxia.[4]

Function

Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. It is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. The COX4I2 nuclear gene encodes isoform 2 of subunit IV. Isoform 1 of subunit IV is encoded by a different gene, however, the two genes show a similar structural organization. Subunit IV is the largest nuclear encoded subunit which plays a pivotal role in COX regulation. It is located on the inner mitochondrial membrane on the matrix side. Expression of COX4I2 is highest in the placenta and the lungs.[3][7][8] Additionally, the expression of COX4I2, along with COX4I1, may be regulated by oxygen levels, with reduced levels of oxygen leading to increased COX4I2 expression and COX4I1 degradation. This suggests a role for COX4I2 in the optimization of the electron transfer chain under different conditions.[9]

Clinical Significance

Mutations in COX4I2 have been associated with exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis (EPIDACH). Characteristics of this disease include pancreatic insufficiency, intestinal malabsorption, failure to thrive, and anemia soon after birth. Additional symptoms have included steatorrhea, splenomegaly and hepatomegaly, pancreatic atrophy, generalized muscle hypotonia, hyperostosis, yellowish sclera associated with mild indirect hyperbilirubinemia, impaired coagulation functions, elevated LDH, alanine, and bilirubin, and reduced vitamin E levels. A homozygous mutation, E138K, has been found to result in reduced COX4I2 expression (25% in fibroblasts) and an impaired response to hypoxia. Functional COX4I2 expression below 40% of its normal level is predicted to be rate-limiting, with the E138K mutation occurring in what is believed to be a highly conserved residue of subunit IV.[7][8][4]

Interactions

COX4I2 has been shown to interact with Cytochrome c (CYCS).[10][11][12][13] Additionally, APP, COA3, and KRAS have been found to have protein-protein interactions with COX4I2.[14]

References

1. ^{{cite journal | vauthors = Hüttemann M, Kadenbach B, Grossman LI | title = Mammalian subunit IV isoforms of cytochrome c oxidase | journal = Gene | volume = 267 | issue = 1 | pages = 111–23 | date = April 2001 | pmid = 11311561 | pmc = | doi = 10.1016/S0378-1119(01)00385-7 }}
2. ^{{cite journal | vauthors = Hüttemann M, Lee I, Liu J, Grossman LI | title = Transcription of mammalian cytochrome c oxidase subunit IV-2 is controlled by a novel conserved oxygen responsive element | journal = The FEBS Journal | volume = 274 | issue = 21 | pages = 5737–48 | date = November 2007 | pmid = 17937768 | pmc = | doi = 10.1111/j.1742-4658.2007.06093.x }}
3. ^1 2 {{cite web|url=https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=84701|title=Entrez Gene: COX4I2 cytochrome c oxidase subunit IV isoform 2 (lung)|access-date=}}{{PD-notice}}
4. ^1 2 {{cite journal | vauthors = Shteyer E, Saada A, Shaag A, Al-Hijawi FA, Kidess R, Revel-Vilk S, Elpeleg O | title = Exocrine pancreatic insufficiency, dyserythropoeitic anemia, and calvarial hyperostosis are caused by a mutation in the COX4I2 gene | journal = American Journal of Human Genetics | volume = 84 | issue = 3 | pages = 412–7 | date = March 2009 | pmid = 19268275 | pmc = 2668012 | doi = 10.1016/j.ajhg.2009.02.006 }}
5. ^{{cite journal | vauthors = Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P | title = Integration of cardiac proteome biology and medicine by a specialized knowledgebase | journal = Circulation Research | volume = 113 | issue = 9 | pages = 1043–53 | date = October 2013 | pmid = 23965338 | pmc = 4076475 | doi = 10.1161/CIRCRESAHA.113.301151 }}
6. ^{{Cite web|url=https://amino.heartproteome.org/web/protein/Q96KJ9|title=Cardiac Organellar Protein Atlas Knowledgebase (COPaKB) —— Protein Information|last=Yao|first=Daniel|website=amino.heartproteome.org|access-date=2018-08-06}}
7. ^1 2 {{Cite web|url=https://www.uniprot.org/uniprot/Q96KJ9|title=COX4I2 - Cytochrome c oxidase subunit 4 isoform 2, mitochondrial precursor - Homo sapiens (Human) - COX4I2 gene & protein|website=www.uniprot.org|language=en|access-date=2018-08-06}}{{CC-notice|cc=by4}}
8. ^1 2 {{cite journal | vauthors = | title = UniProt: the universal protein knowledgebase | journal = Nucleic Acids Research | volume = 45 | issue = D1 | pages = D158-D169 | date = January 2017 | pmid = 27899622 | pmc = 5210571 | doi = 10.1093/nar/gkw1099 | url = https://doi.org/10.1093/nar/gkw1099 }}
9. ^{{cite journal | vauthors = Fukuda R, Zhang H, Kim JW, Shimoda L, Dang CV, Semenza GL | title = HIF-1 regulates cytochrome oxidase subunits to optimize efficiency of respiration in hypoxic cells | journal = Cell | volume = 129 | issue = 1 | pages = 111–22 | date = April 2007 | pmid = 17418790 | doi = 10.1016/j.cell.2007.01.047 }}
10. ^{{cite journal | vauthors = Michel B, Bosshard HR | title = Spectroscopic analysis of the interaction between cytochrome c and cytochrome c oxidase | journal = The Journal of Biological Chemistry | volume = 259 | issue = 16 | pages = 10085–91 | date = August 1984 | pmid = 6088481 }}
11. ^{{cite journal | vauthors = Wiedemann FR, Vielhaber S, Schröder R, Elger CE, Kunz WS | title = Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples | journal = Analytical Biochemistry | volume = 279 | issue = 1 | pages = 55–60 | date = March 2000 | pmid = 10683230 | doi = 10.1006/abio.1999.4434 }}
12. ^{{cite journal | vauthors = Sampson V, Alleyne T | title = Cytochrome c/cytochrome c oxidase interaction. Direct structural evidence for conformational changes during enzyme turnover | journal = European Journal of Biochemistry | volume = 268 | issue = 24 | pages = 6534–44 | date = December 2001 | pmid = 11737208 | doi = 10.1046/j.0014-2956.2001.02608.x }}
13. ^{{cite journal | vauthors = Lynch SR, Sherman D, Copeland RA | title = Cytochrome c binding affects the conformation of cytochrome a in cytochrome c oxidase | journal = The Journal of Biological Chemistry | volume = 267 | issue = 1 | pages = 298–302 | date = January 1992 | pmid = 1309738 }}
14. ^{{Cite web|url=https://thebiogrid.org/124215|title=COX4I2 Result Summary {{!}} BioGRID|last=Lab|first=Mike Tyers|website=thebiogrid.org |access-date=2018-08-06}}

External links

  • {{UCSC gene info|COX4I2}}

Further reading

{{refbegin | 2}}
  • {{cite journal | vauthors = Garber EA, Margoliash E | title = Interaction of cytochrome c with cytochrome c oxidase: an understanding of the high- to low-affinity transition | journal = Biochimica et Biophysica Acta | volume = 1015 | issue = 2 | pages = 279–87 | date = February 1990 | pmid = 2153405 | doi = 10.1016/0005-2728(90)90032-Y }}
  • {{cite journal | vauthors = Bolli R, Nałecz KA, Azzi A | title = The interconversion between monomeric and dimeric bovine heart cytochrome c oxidase | journal = Biochimie | volume = 67 | issue = 1 | pages = 119–28 | date = January 1985 | pmid = 2986725 | doi = 10.1016/S0300-9084(85)80237-6 }}
  • {{cite journal | vauthors = Michel B, Bosshard HR | title = Spectroscopic analysis of the interaction between cytochrome c and cytochrome c oxidase | journal = The Journal of Biological Chemistry | volume = 259 | issue = 16 | pages = 10085–91 | date = August 1984 | pmid = 6088481 | doi = }}
  • {{cite journal | vauthors = Hare JF, Ching E, Attardi G | title = Isolation, subunit composition, and site of synthesis of human cytochrome c oxidase | journal = Biochemistry | volume = 19 | issue = 10 | pages = 2023–30 | date = May 1980 | pmid = 6246917 | doi = 10.1021/bi00551a003 }}
  • {{cite journal | vauthors = Papadopoulou LC, Tsiftsoglou AS | title = Effects of hemin on apoptosis, suppression of cytochrome c oxidase gene expression, and bone-marrow toxicity induced by doxorubicin (adriamycin) | journal = Biochemical Pharmacology | volume = 52 | issue = 5 | pages = 713–22 | date = September 1996 | pmid = 8765469 | doi = 10.1016/0006-2952(96)00349-8 }}
  • {{cite journal | vauthors = Vizirianakis IS, Pappas IS, Tsiftsoglou AS | title = Differentiation-dependent repression of c-myc, B22, COX II and COX IV genes in murine erythroleukemia (MEL) cells | journal = Biochemical Pharmacology | volume = 63 | issue = 5 | pages = 1009–17 | date = March 2002 | pmid = 11911854 | doi = 10.1016/S0006-2952(01)00937-6 }}
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