Wikipedia

COX7B

Cytochrome c oxidase subunit 7B, mitochondrial (COX7B) is an enzyme that in humans is encoded by the COX7B gene.[5] COX7B is a nuclear-encoded subunit of cytochrome c oxidase (COX). 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.[6] Work with Oryzias latices has linked disruptions in COX7B with microphthalmia with linear skin lesions (MLS), microcephaly, and mitochondrial disease. Clinically, mutations in COX7B have been associated with linear skin defects with multiple congenital anomalies.[7]

COX7B
Identifiers
AliasesCOX7B, APLCC, LSDMCA2, cytochrome c oxidase subunit 7B
External IDsOMIM: 300885; MGI: 1913392; HomoloGene: 1406; GeneCards: COX7B; OMA:COX7B - orthologs
Orthologs
SpeciesHumanMouse
Entrez

1349

66142

Ensembl

ENSG00000131174

ENSMUSG00000031231

UniProt

P24311

P56393

RefSeq (mRNA)

NM_001866

NM_025379

RefSeq (protein)

NP_001857

NP_079655

Location (UCSC)Chr X: 77.9 – 77.91 MbChr X: 105.06 – 105.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Structure

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COX7B is located on the q arm of the X chromosome in position 21.1 and has 3 exons.[6] The COX7B gene produces a 9.2 kDa protein composed of 80 amino acids.[8][9] COX7B is one of the nuclear-encoded polypeptide chains of cytochrome c oxidase (COX), a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The protein encoded by COX7B belongs to the cytochrome c oxidase VIIb family. COX7B has a 24 amino acid transit peptide domain from positions 1-24, an 8 amino acid topological mitochondrial matrix domain from positions 25–32, a helical, 27 amino acid transmembrane domain from positions 33–59, and a 21 amino acid topological intermembrane domain from positions 60–80.[10][11][12][7] COX7B may also have several pseudogenes on chromosomes 1, 2, 20 and 22.[6]

Function

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Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. The mitochondrially-encoded subunits of COX function in electron transfer, while the nuclear-encoded subunits may be involved in the regulation and assembly of the complex. The COX7B nuclear gene encodes subunit 7B, which is located on the inner mitochondrial membrane in association with several other proteins encompassing the COX complex. It is found in all tissues and has been shown to be highly similar to bovine COX VIIb protein.[6] COX7B is believed to be important for COX assembly and activity, the function of mitochondrial respiratory chain, and the proper development of the central nervous system in vertebrates.[7][10][11]

Model organisms

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Oryzias latices (also known as medaka) is a Japanese rice fish that has been used as a model organism in COX7B studies. By using a morpholino knockdown technique, COX7B has been shown to be indispensable for COX assembly, COX activity, and mitochondrial respiration. Additionally, the down-regulation of an ortholog of COX7B has suggested that there may be an association between COX7B dysfunction and microphthalmia with linear skin lesions (MLS), microcephaly, and mitochondrial disease. Work with Oryzias latices could also indicate an evolutionary conserved role for the mitochondrial respiratory chain complexes in central nervous system development.[7]

Clinical significance

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Mutations in COX7B have been associated with linear skin defects with multiple congenital anomalies. This disorder is a distinct form of aplasia cutis congenita presenting as multiple linear skin defects on the face and neck associated with poor growth and short stature, microcephaly, and facial dysmorphism. Additional clinical features include intellectual disability, nail dystrophy, cardiac abnormalities, diaphragmatic hernia, genitourinary abnormalities, pale optic discs and altered visual-evoked potentials, agenesis of the corpus callosum, and other central nervous system abnormalities.[10][11] The COX7B mutations associated with disease include c.196delC, a heterozygous mutation leading to a frameshift in exon 3, c.41-2A>G, a heterozygous splice mutation in a novel acceptor site in intron 1, and c.55C>T, a heterozygous nonsense mutation in exon 2. Additionally, experiments with Oryzias latices suggest COX7B may be associated with microphthalmia with linear skin lesions (MLS), an X-linked, dominant, male-lethal mitochondrial disorder.[7]

Interactions

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COX7B has been shown to have 6 binary protein-protein interactions including 3 co-complex interactions. GNMT, MYB, MT-CO1, HSCB, and SLC25A13 have all been found to interact with COX7B.[13]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000131174 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031231 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Sadlock JE, Lightowlers RN, Capaldi RA, Schon EA (February 1993). "Isolation of a cDNA specifying subunit VIIb of human cytochrome c oxidase". Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1172 (1–2): 223–5. doi:10.1016/0167-4781(93)90301-s. PMID 8382530.
  6. ^ a b c d "Entrez Gene: COX7B cytochrome c oxidase subunit VIIb".  This article incorporates text from this source, which is in the public domain.
  7. ^ a b c d e Indrieri A, van Rahden VA, Tiranti V, Morleo M, Iaconis D, Tammaro R, D'Amato I, Conte I, Maystadt I, Demuth S, Zvulunov A, Kutsche K, Zeviani M, Franco B (November 2012). "Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease". American Journal of Human Genetics. 91 (5): 942–9. doi:10.1016/j.ajhg.2012.09.016. PMC 3487127. PMID 23122588.
  8. ^ Yao, Daniel. "Cardiac Organellar Protein Atlas Knowledgebase (COPaKB) —— Protein Information". amino.heartproteome.org. Retrieved 2018-08-06.[permanent dead link‍]
  9. ^ 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 (October 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
  10. ^ a b c "COX7B - Cytochrome c oxidase subunit 7B, mitochondrial precursor - Homo sapiens (Human) - COX7B gene & protein". uniprot.org. Retrieved 2018-08-06.  This article incorporates text available under the CC BY 4.0 license.
  11. ^ a b c "UniProt: the universal protein knowledgebase". Nucleic Acids Research. 45 (D1): D158–D169. January 2017. doi:10.1093/nar/gkw1099. PMC 5210571. PMID 27899622.
  12. ^ Van Kuilenburg AB, Van Beeumen JJ, Van der Meer NM, Muijsers AO (January 1992). "Subunits VIIa,b,c of human cytochrome c oxidase. Identification of both 'heart-type' and 'liver-type' isoforms of subunit VIIa in human heart". European Journal of Biochemistry. 203 (1–2): 193–9. doi:10.1111/j.1432-1033.1992.tb19847.x. PMID 1309697.
  13. ^ "6 binary interactions found for search term COX7B". IntAct Molecular Interaction Database. EMBL-EBI. Retrieved 2018-08-25.
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Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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