UBIAD1

UBIAD1
Identifiers
Aliases	UBIAD1, SCCD, TERE1, UbiA prenyltransferase domain containing 1
External IDs	OMIM: 611632; MGI: 1918957; GeneCards: UBIAD1
Enzyme activity
Gene location (Human)
Chr.	Chromosome 1 (human)
End	11,296,049 bp
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	148,529,228 bp
RNA expression pattern
	Top expressed in
	gastrocnemius muscle; ; muscle of thigh; ; gonad; ; secondary oocyte; ; skin of thigh; ; ganglionic eminence; ; islet of Langerhans; ; nipple; ; granulocyte; ; ventricular zone;
	Top expressed in
	zygote; ; proximal tubule; ; right kidney; ; secondary oocyte; ; primary oocyte; ; human kidney; ; interventricular septum; ; yolk sac; ; muscle of thigh; ; Rostral migratory stream;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	transferase activity; antioxidant activity; protein binding; prenyltransferase activity; transferase activity, transferring alkyl or aryl (other than methyl) groups;
Cellular component	cytoplasm; integral component of membrane; integral component of Golgi membrane; Golgi apparatus; endoplasmic reticulum membrane; membrane; mitochondrial membranes; Golgi membrane; endoplasmic reticulum; mitochondrion; nucleus;
Biological process	menaquinone biosynthetic process; ubiquinone biosynthetic process; vitamin K biosynthetic process; vitamin K metabolic process; cellular oxidant detoxification; ubiquinone biosynthetic process via 3,4-dihydroxy-5-polyprenylbenzoate;
	Sources:Amigo / QuickGO
Orthologs
Databases	NCBI: entry; OMA: entry
	29914
	71707
	ENSG00000120942
	ENSMUSG00000047719
	Q9Y5Z9
	Q9DC60
	NM_013319; NM_001330349; NM_001330350
	NM_027873
	NP_001317278; NP_001317279; NP_037451
	NP_082149
	Wikidata
View/Edit Human	View/Edit Mouse

UbiA prenyltransferase domain-containing protein 1 (UBIAD1) also known as transitional epithelial response protein 1 (TERE1) is a protein that in humans is encoded by the UBIAD1 gene.

The enzyme is named for its canonical role in ubiquinone production, catalyzing reaction EC 2.5.1.39; it thus has a role in oxidative stress pathways.

Recent evidence suggests that UBIAD1 has enzymatic activity in the vitamin K pathway, converting menadione to MK-4. This translates to a role in blood vessel development in zebrafish.

Clinical significance

Mutations of the UBIAD1 gene cause Schnyder crystalline corneal dystrophy.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000120942 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000047719 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ McGarvey TW, Nguyen T, Puthiyaveettil R, Tomaszewski JE, Malkowicz SB (December 2002). "TERE1, a novel gene affecting growth regulation in prostate carcinoma". The Prostate. 54 (2): 144–155. doi:10.1002/pros.10174. PMID 12497587. S2CID 12942882.
↑ McGarvey TW, Nguyen T, Tomaszewski JE, Monson FC, Malkowicz SB (April 2001). "Isolation and characterization of the TERE1 gene, a gene down-regulated in transitional cell carcinoma of the bladder". Oncogene. 20 (9): 1042–1051. doi:10.1038/sj.onc.1204143. PMID 11314041.
↑ "Entrez Gene: UBIAD1 UbiA prenyltransferase domain containing 1".
↑ Fredericks WJ, McGarvey T, Wang H, Lal P, Puthiyaveettil R, Tomaszewski J, et al. (November 2011). "The bladder tumor suppressor protein TERE1 (UBIAD1) modulates cell cholesterol: implications for tumor progression". DNA and Cell Biology. 30 (11): 851–864. doi:10.1089/dna.2011.1315. PMC 3206744. PMID 21740188.
↑ Hirota Y, Tsugawa N, Nakagawa K, Suhara Y, Tanaka K, Uchino Y, et al. (November 2013). "Menadione (vitamin K3) is a catabolic product of oral phylloquinone (vitamin K1) in the intestine and a circulating precursor of tissue menaquinone-4 (vitamin K2) in rats". The Journal of Biological Chemistry. 288 (46): 33071–33080. doi:10.1074/jbc.M113.477356. PMC 3829156. PMID 24085302.
↑ Nakagawa K, Hirota Y, Sawada N, Yuge N, Watanabe M, Uchino Y, et al. (November 2010). "Identification of UBIAD1 as a novel human menaquinone-4 biosynthetic enzyme". Nature. 468 (7320): 117–121. Bibcode:2010Natur.468..117N. doi:10.1038/nature09464. PMID 20953171. S2CID 9385489.
↑ Postel R (May 2008). Identification and Characterization of Novel Genes by Reverse and Forward Genetics in Zebrafish (Ph.D. thesis). Utrecht University.
↑ Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, White PS, Winters RS, et al. (November 2007). "Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy". Investigative Ophthalmology & Visual Science. 48 (11): 5007–5012. doi:10.1167/iovs.07-0845. PMID 17962451.
↑ Orr A, Dubé MP, Marcadier J, Jiang H, Federico A, George S, et al. (August 2007). "Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy". PLOS ONE. 2 (8): e685. Bibcode:2007PLoSO...2..685O. doi:10.1371/journal.pone.0000685. PMC 1925147. PMID 17668063.
↑ Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, et al. (February 2008). "Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function". American Journal of Medical Genetics. Part a. 146 (3): 271–283. doi:10.1002/ajmg.a.32201. PMID 18176953. S2CID 24627267.

Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
McGarvey TW, Nguyen TB, Malkowicz SB (2005). "An interaction between apolipoprotein E and TERE1 with a possible association with bladder tumor formation". Journal of Cellular Biochemistry. 95 (2): 419–428. doi:10.1002/jcb.20432. PMID 15782423. S2CID 43563999.
Otsuki T, Ota T, Nishikawa T, Hayashi K, Suzuki Y, Yamamoto J, et al. (2005). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Research. 12 (2): 117–126. doi:10.1093/dnares/12.2.117. PMID 16303743.
Yellore VS, Khan MA, Bourla N, Rayner SA, Chen MC, Sonmez B, et al. (September 2007). "Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy". Molecular Vision. 13: 1777–1782. PMID 17960116.

This article on a gene on human chromosome 1 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000120942 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000047719 – 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.

[McGarvey_2002-5] McGarvey TW, Nguyen T, Puthiyaveettil R, Tomaszewski JE, Malkowicz SB (December 2002). "TERE1, a novel gene affecting growth regulation in prostate carcinoma". The Prostate. 54 (2): 144–155. doi:10.1002/pros.10174. PMID 12497587. S2CID 12942882.

[McGarvey_2001-6] McGarvey TW, Nguyen T, Tomaszewski JE, Monson FC, Malkowicz SB (April 2001). "Isolation and characterization of the TERE1 gene, a gene down-regulated in transitional cell carcinoma of the bladder". Oncogene. 20 (9): 1042–1051. doi:10.1038/sj.onc.1204143. PMID 11314041.

[entrez-7] "Entrez Gene: UBIAD1 UbiA prenyltransferase domain containing 1".

[Fredericks_2011-8] Fredericks WJ, McGarvey T, Wang H, Lal P, Puthiyaveettil R, Tomaszewski J, et al. (November 2011). "The bladder tumor suppressor protein TERE1 (UBIAD1) modulates cell cholesterol: implications for tumor progression". DNA and Cell Biology. 30 (11): 851–864. doi:10.1089/dna.2011.1315. PMC 3206744. PMID 21740188.

[nat-9] Hirota Y, Tsugawa N, Nakagawa K, Suhara Y, Tanaka K, Uchino Y, et al. (November 2013). "Menadione (vitamin K3) is a catabolic product of oral phylloquinone (vitamin K1) in the intestine and a circulating precursor of tissue menaquinone-4 (vitamin K2) in rats". The Journal of Biological Chemistry. 288 (46): 33071–33080. doi:10.1074/jbc.M113.477356. PMC 3829156. PMID 24085302.

[Nakagawa_2010-10] Nakagawa K, Hirota Y, Sawada N, Yuge N, Watanabe M, Uchino Y, et al. (November 2010). "Identification of UBIAD1 as a novel human menaquinone-4 biosynthetic enzyme". Nature. 468 (7320): 117–121. Bibcode:2010Natur.468..117N. doi:10.1038/nature09464. PMID 20953171. S2CID 9385489.

[11] Postel R (May 2008). Identification and Characterization of Novel Genes by Reverse and Forward Genetics in Zebrafish (Ph.D. thesis). Utrecht University.

[Weiss_2007-12] Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, White PS, Winters RS, et al. (November 2007). "Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy". Investigative Ophthalmology & Visual Science. 48 (11): 5007–5012. doi:10.1167/iovs.07-0845. PMID 17962451.

[Orr_2007-13] Orr A, Dubé MP, Marcadier J, Jiang H, Federico A, George S, et al. (August 2007). "Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy". PLOS ONE. 2 (8): e685. Bibcode:2007PLoSO...2..685O. doi:10.1371/journal.pone.0000685. PMC 1925147. PMID 17668063.

[Weiss_2008-14] Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, et al. (February 2008). "Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function". American Journal of Medical Genetics. Part a. 146 (3): 271–283. doi:10.1002/ajmg.a.32201. PMID 18176953. S2CID 24627267.

UBIAD1

Clinical significance

References

Further reading