CHST6

From Wikipedia, the free encyclopedia

Carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6

Identifiers

External IDs

OMIM: 605294 MGI: 1931825 HomoloGene: 56927

Gene ontology
Molecular Function:	• N-acetylglucosamine 6-O-sulfotransferase activity • transferase activity
Cellular Component:	• Golgi apparatus • membrane • integral to membrane • intrinsic to Golgi membrane
Biological Process:	• carbohydrate metabolic process • N-acetylglucosamine metabolic process • sulfur metabolic process • keratan sulfate biosynthetic process

Orthologs

Human

Mouse

Refseq

NM_021615 (mRNA)
NP_067628 (protein)

NM_019950 (mRNA)
NP_064334 (protein)

Location

Chr 16: 74.06 - 74.09 Mb

Chr 8: 114.78 - 114.8 Mb

Pubmed search

[1]

[2]

Carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6, also known as CHST6, is a human gene.^[1]

[edit] References

^ Entrez Gene: CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6.

[edit] Further reading

Bernstein HB, Compans RW (1992). "Sulfation of the human immunodeficiency virus envelope glycoprotein.". J. Virol. 66 (12): 6953-9. PMID 1433500.
Shilatifard A, Merkle RK, Helland DE, et al. (1993). "Complex-type N-linked oligosaccharides of gp120 from human immunodeficiency virus type 1 contain sulfated N-acetylglucosamine.". J. Virol. 67 (2): 943-52. PMID 8419650.
Vance JM, Jonasson F, Lennon F, et al. (1996). "Linkage of a gene for macular corneal dystrophy to chromosome 16.". Am. J. Hum. Genet. 58 (4): 757-62. PMID 8644739.
Uchimura K, Fasakhany F, Kadomatsu K, et al. (2000). "Diversity of N-acetylglucosamine-6-O-sulfotransferases: molecular cloning of a novel enzyme with different distribution and specificities.". Biochem. Biophys. Res. Commun. 274 (2): 291-6. doi:10.1006/bbrc.2000.3141. PMID 10913333.
Akama TO, Nishida K, Nakayama J, et al. (2000). "Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene.". Nat. Genet. 26 (2): 237-41. doi:10.1038/79987. PMID 11017086.
Spiro MJ, Spiro RG (2001). "Sulfation of the N-linked oligosaccharides of influenza virus hemagglutinin: temporal relationships and localization of sulfotransferases.". Glycobiology 10 (11): 1235-42. PMID 11087716.
Liu NP, Dew-Knight S, Rayner M, et al. (2001). "Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.". Mol. Vis. 6: 261-4. PMID 11139648.
Hemmerich S, Lee JK, Bhakta S, et al. (2001). "Chromosomal localization and genomic organization for the galactose/ N-acetylgalactosamine/N-acetylglucosamine 6-O-sulfotransferase gene family.". Glycobiology 11 (1): 75-87. PMID 11181564.
Akama TO, Nakayama J, Nishida K, et al. (2001). "Human corneal GlcNac 6-O-sulfotransferase and mouse intestinal GlcNac 6-O-sulfotransferase both produce keratan sulfate.". J. Biol. Chem. 276 (19): 16271-8. doi:10.1074/jbc.M009995200. PMID 11278593.
Bartes A, Bhakta S, Hemmerich S (2001). "Sulfation of endothelial mucin by corneal keratan N-acetylglucosamine 6-O-sulfotransferase (GST-4beta).". Biochem. Biophys. Res. Commun. 282 (4): 928-33. doi:10.1006/bbrc.2001.4668. PMID 11352640.
El-Ashry MF, Abd El-Aziz MM, Wilkins S, et al. (2002). "Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy.". Invest. Ophthalmol. Vis. Sci. 43 (2): 377-82. PMID 11818380.
Akama TO, Misra AK, Hindsgaul O, Fukuda MN (2003). "Enzymatic synthesis in vitro of the disulfated disaccharide unit of corneal keratan sulfate.". J. Biol. Chem. 277 (45): 42505-13. doi:10.1074/jbc.M207412200. PMID 12218059.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932.
Niel F, Ellies P, Dighiero P, et al. (2003). "Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophy.". Invest. Ophthalmol. Vis. Sci. 44 (7): 2949-53. PMID 12824236.
Iida-Hasegawa N, Furuhata A, Hayatsu H, et al. (2003). "Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.". Invest. Ophthalmol. Vis. Sci. 44 (8): 3272-7. PMID 12882769.
Ha NT, Chau HM, Cung le X, et al. (2003). "Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.". Invest. Ophthalmol. Vis. Sci. 44 (8): 3310-6. PMID 12882775.
Ha NT, Chau HM, Cung le X, et al. (2003). "Identification of novel mutations of the CHST6 gene in Vietnamese families affected with macular corneal dystrophy in two generations.". Cornea 22 (6): 508-11. PMID 12883341.
Warren JF, Aldave AJ, Srinivasan M, et al. (2003). "Novel mutations in the CHST6 gene associated with macular corneal dystrophy in southern India.". Arch. Ophthalmol. 121 (11): 1608-12. doi:10.1001/archopht.121.11.1608. PMID 14609920.
Sultana A, Sridhar MS, Jagannathan A, et al. (2004). "Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India.". Mol. Vis. 9: 730-4. PMID 14735064.
Abbruzzese C, Kuhn U, Molina F, et al. (2004). "Novel mutations in the CHST6 gene causing macular corneal dystrophy.". Clin. Genet. 65 (2): 120-5. PMID 14984470.