Localization of a locus (GLC1B) for adult-onset primary open angle glaucoma to the 2cen-q13 region

Genomics

Volumn 36, Issue 1, 1996, Pages 142-150

  Stoilova, Diliana ^a,c   Child, Anne ^b,c   Trifan, Ovidiu C ^a,c   Crick, R Pitts ^c   Coakes, Roger L ^c   Sarfarazi, Mansoor ^a,c  

^a UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

^b ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^c KING S COLLEGE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 1Q; CHROMOSOME 2; CHROMOSOME MAP; GENE LOCUS; HUMAN; HUMAN CELL; INTRAOCULAR HYPERTENSION; MAJOR CLINICAL STUDY; OPEN ANGLE GLAUCOMA; OPTIC NERVE DISEASE; PRIORITY JOURNAL; VISUAL FIELD DEFECT;

EID: 0030586892     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0434     Document Type: Article

References (63)

1. Akarsu, A. N., Turacli, M. E., Aktan, S. G., Barsoum-Homsy, M., Chevrette, L., Sayli, B. S., and Sarfarazi, M. (1996a). A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region. Hum. Mol. Genet., in press.
2. Akarsu, A. N., Turacli, M. E., Aktan, S. G., Hossain, A., Barsoum-Homsy, M., Chevrette, L., Sayli, B. S., and Sarfarazi, M. (1996b). Exclusion of primary congenital glaucoma from two candidate regions of chromosome arm 6p and chromosome 11. Am. J. Med. Genet. 61: 290-292. [Erratum 62: 102].
3. Bassam, B. S., and Caetano-Annoles, G. (1993). Silver staining of DNA in polyacrylamide gels. Protocols Biotechnol. 42: 181-188.
4. Beiguelman, B., and Prado, D. (1963). Recessive juvenile glaucoma. J. Genet. Hum. 12: 53-54.
5. Bennett, S. R., Alward, W. L., and Folberg, R. (1989). An autosomal dominant form of low tension glaucoma. Am. J. Ophthalmol. 108: 238-244.
6. Bowcock, A. M., Kavathas, P., Margolskee, R. F., Herzenburg, L., and Cavalli-Sforza, L. L. (1986). An RFLP associated with pcDLeu2-14, a human T-cell differentiation antigen CD8 (Leu2) cDNA mapped to 2p12. Nucleic Acids Res. 14: 7817.
7. Copeland, N. G., Silan, C. M., Kingsley, D. M., Jenkins, N. A., Cannisaro, L. A., Croce, C. M., Huebner, K., and Sims, J. E. (1991). Chromosomal location of murine and human IL-1 receptor genes. Genomics 9: 44-50.
8. Crick, R. P. (1974). Chronic glaucoma. A preventable cause of blindness. Lancet 1: 205-207.
9. Crick, R. P., and Blackmore, H. (1979). The King's College Hospital clinical data base for glaucoma. In "Proceedings of Symposium on Computers in Ophthalmology" (R. H. Greenfield and A. Colenbrander, Eds.), No. 79, CH 1717-2C, pp. 51-59. IEEE Computer Society New York, St. Louis.
10. Crick, R. P., and Daubs, J. G. (1980). Epidemiological aids to clinical decision making in primary open angle glaucoma. Int. Ophthalmol. 3: 37-41.
11. Crick, R. P., Reynolds, P. M., and Daubs, J. G. (1983). Epidemiological aspects of primary open angle glaucoma. Glaucoma 5: 4-14.
12. Crick, R. P., Vogel, R., Newson, R. B., Shipley, M. J., Blackmore, H., Palmer, A., and Bulpitt, C. J. (1989). The visual field in chronic simple glaucoma and ocular hypertension; its character, progress relationship to the level of intraocular pressure and response to treatment. Eye 3: 536-546.
13. Crombie, A. L., and Cullen, J. F. (1964). Hereditary glaucoma: Occurrence in five generations in an Edinburgh family. Br. J. Ophthalmol. 48: 143-147.
14. Dib, C., Faure, S., Fizames, C., Samson, D., Drouot, N., Vignal, A., Millasseau, P., Marc, S., Kazan, J., Seboun, E., Lathrop, M., Gyapay, G., Morissette, J., and Weissenbach, J. (1996). The final version of the Généthon human genetic linkage map. Nature 380: 152-154.
15. Ellis, O. H. (1948). The etiology, symptomatology and treatment of juvenile glaucoma. Am. J. Ophthalmol. 31: 1589-1596.
16. Fasman, K. H., Aeticchia, A. J., and Kingsbury, D. T. (1994). The GDB Human Genome Data Base anno 1994. Nucl. Acids Res. 22(17): 3462-3469.
17. Gastier, J. M., Pulido, J. C., Sunden, S., Brody, T., Buetow, K. H., Murray, J. C., Weber, J. L., Hudson, T. J., Sheffield, V. C., and Duyk, G. M. (1995). Survey of trinucleotide repeats in the human genome: Assessment of their utility as genetic markers. Hum. Mol. Genet. 4: 1829-1836.
18. Goldwyn, R., Waltman, S. R., and Becker, B. (1970). Primary open-angle glaucoma in adolescent and young adults. Arch. Ophthalmol. 84: 579-582.
19. Graff, C., Urbak, S. F., Jerndal, T., and Wadelius, C. (1995). Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity. Hum. Genet. 96: 285-289.
20. Grosskreutz, C., and Netland, P. A. (1994). Low tension glaucoma. Int. Ophthalmol. Clin. 34(3): 173-185.
21. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-94 Généthon human genetic linkage map. Nature Genet. 7(Suppl.): 246-339.
22. Hitchings, R. A. (1992). Low tension glaucoma - Its place in modern glaucoma practice. Br. J. Ophthalmol. 76: 494-496.
23. Hsieh, C. L., Swaroop, A., and Francke, U. (1990). Chromosomal location and cDNA sequence of human RALB, a GTP binding protein. Somat. Cell Mol. Genet. 16: 407-410.
24. Hudson, T., Stein, L., Gerety, S., Ma, J., Castle, A., Silva, J., Slonim, D., Baptista, R., Kruglyak, L., Xu, S., Hu, X., Colbert, A., Rosenberg, C., Reeve-Daly, M. P., Rozen, S., Hui, L., Wu, X., Vestergaard, C., Wilson, K., Bae, J., Maitra, S., Ganiatsas, S., Evans, C., DeAngelis, M., Ingalls, K., Nahf, R., Horton, L., Oskin, M., Collymore, A., Ye, W., Kouyoumjian, V., Zernsteva, I., Tarn, J., Devine, R., Courtney, D., Renaud, M., Nguyen, H., O'Connor, T., Fizames, C., Faure, S., Gyapay, G., Dib, C., Morissette, J., Orlin, J., Birren, B., Goodman, N., Weissenbach, J., Hawkins, T., Foote, S., Page, D., and Lander, E. (1995). An STS-based map of the human genome. Science 270: 1945-1954.
25. Jay, B., and Peterson, G. (1970). The genetics of simple glaucoma. Trans. Ophthalmol. Soc. UK 90: 161-171.
26. Jay, J. L., and Murdoch, J. R. (1993). The rate of visual field loss in untreated primary open angle glaucoma. Br. J. Ophthalmol. 77: 176-178.
27. Johnson, A. T., Drack, A. V., Kwitek, A. E., Cannon, R. L., Stone, E. M., and Alward, W. L. M (1993). Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma. Ophthalmology 100: 524-529.
28. Kohler, A., Logan, C., Joyner, A. L., and Muenke, M. (1993). Regional assignment of the human homeobox-containing gene EN1 to chromosome 2q13-q21. Genomics 15: 233-235.
29. Lathrop, G. M., and Lalouel, J. M. (1984). Easy calculations of lod scores and genetic risks on small computers. Am. J. Hum. Genet. 36: 460-465.
30. Lee, D. A., Brubaker, R. F., and Hrusca, L. (1985). Hereditary glaucoma: A report of two pedigrees. Ann. Ophthalmol. 17: 739-741.
31. Leske, M. C. (1983). The epidemiology of open angle glaucoma; A review. Am. J. Epidemiol. 118: 166-191.
32. Lichter, P. R. (1994). Genetic clues to glaucoma's secrets. The Jackson memorial lecture. Part 2. Am. J. Ophthalmol. 117: 706-727.
33. Lomasney, J. W., Lorenz, W., Allen, L. F., King, K., Regan, J. W., Yang-Feng, T. L., Caron, M. G., and Lefkowitz, R. J. (1990). Expansion of the alpha-2-adrenergic receptor family: Cloning and characterization of a human alpha-2-adrenergic receptor subtype, the gene for which is located on chromosome 2. Proc. Natl. Acad. Sci. USA 87: 5094-5098.
34. Meyer, A., Valtot, F., Bechetoille, A., Rouland, J.-F., Dascotte, J.-C., Ferec, C., Bach, J., Chaventre, A., and Garchon, H. (1994). Linkage between juvenile glaucoma and chromosome 1q in two French families. Comp. Rend. Acad. Sci. (Paris) 317: 565-570.
35. Miller, R. (1978). Genetics of glaucoma and family studies. Trans. Ophthalmol. Soc. UK 98: 290-292.
36. Morissette, J., Cote, G., Anctil, J-L., Plante, M., Amyot, M., Heon, E., Trope, G. E., Weissenbach, J., and Raymond, V. (1995). A common gene for juvenile and adult onset primary open-angle glaucomas confines on chromosome 1q. Am. J. Hum. Genet. 56: 1431-1442.
37. Murray, J. C., Buetow, K. H., Weber, J. L., Ludwigsen, S., Scherpbier-Heddema, T., Manion, F., Quillen, J., Sheffield, V. C., Sunden, S., Duyk, G. M., Weissenbach, J., Gyapay, G., Dib, C., Morrissette, J., Lathrop, G. M., Vignal, A., White, R., Matsunami, N., Gerken, S., Melis, R., Albertsen, H., Plaetke, R., Odelberg, S., Ward, D., Dausset, J., Cohen, D., and Cann, H. (1994). A comprehensive human linkage map with centimorgan density. Science 265: 2049-2054.
38. Netland, P. A., Wiggs, J. L., and Dreyer, E. B. (1993). Inheritance of glaucoma and genetic counseling of glaucoma patients. Int. Ophthalmol Clin. 33: 101-120.
39. Ott, J. (1983). Linkage analysis and family classification under heterogeneity. Ann. Hum. Genet. 47: 311.
40. Quigley, H. A. (1993). Open-angle glaucoma. N. Engl. J. Med. 328: 1097-1106.
41. Richards, E. S. (1994). "Current Protocols in Molecular Biology" (R. M. Ausubel, et al., Eds.), John Wiley, New York.
42. Richards, J. E., Lichter, P. R., Boehnke, M., Uro, J. L. A., Torrez, D., Wong, D., and Johnson, A. T. (1994). Mapping of a gene for autosomal dominant juvenile-onset open-angle glaucoma to chromosome 1q. Am. J. Hum. Genet. 54: 62-70.
43. Richards, J. E., Lichter, P. R., Herman, S., Hauser, E., Hou, Y-C., Johnson, A. T., and Boehnke, M. (1996). Genetics of middle-age onset primary open angle glaucoma. Invest. Ophthalmol. Visual Sci. 37(3): p. S34 [Abstract 155].
44. Sarfarazi, M., Akarsu, A. N., Hossain, A., Turacli, M. E., Aktan, S. G., Barsoum-Homsy, M., Chevrette, L., and Sayli, B. S. (1995). Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 30: 171-177.
45. Schaffer, A. A., Gupta, S. K., Shriram, K., and Cottingham, R. W., Jr. (1994). Avoiding recomputation in genetic linkage analysis. Hum. Hered. 44: 225-237.
46. Seghatoleslami, M. R., Child., A., Fossarelo, M., Crick, R. P., and Sarfarazi, M. (1994). Fine mapping of juvenile primary open angle glaucoma (POAG) on 1q21-q31 and exclusion of adult-POAG from the respective region. Am. J. Hum. Genet. 55: p. A203 [Abstract 1179].
47. Seghatoleslami, M. R., Stoilova, D., Child., A., Crick, R. P., and Sarfarazi, M. (1995). Exclusion mapping of the adult-onset primary open angle glaucoma (POAG). Invest. Ophthalmol. Visual Sci. 36(4): p. S1034 [Abstract 4792].
48. Sheffield, V. C., Stone, E. M., Alward, W. L. M., Drack, A. V., Johnson, A. T., Streb, L. M., and Nichols, B. E. (1993). Genetic linkage of familial open-angle glaucoma to chromosome 1q21-q31. Nature Genet. 4: 47-50.
49. Sheffield, V. C., Weber, J. L., Buetow, K. H., Murray, J. C., Even, D. A., Wiles, K., Gastier, J. M., Pulido, J. C., Yandava, C., Sunden, S. L., Mattes, G., Businga, T., McClain, A., Beck, J., Scherpier, T., Gilliam, J., Zhong, J., and Duyk, G. (1995). A collection of tri-and tetranucleotide repeat markers used to generate high quality, high resolution human genomewide linkage maps. Hum. Mol. Genet. 4: 1837-1844.
50. Shin, D. H., Becker, B., and Kolker, A. E. (1977). Family history in primary open-angle glaucoma. Arch. Ophthalmol. 95: 598-600.
51. Sommer, A., Tielsch, J. M., Katz, J., Quigley, H. J., Gottsch, J. D., Javitt, J., and Singh, K. (1991). Relationship between intraocular pressure and primary open angle glaucoma among white and black Americans. Arch. Ophthalmol. 109: 1090-1095.
52. Srivastava, M., McBride, O. W., Fleming, P. J., Pollard, H. B., and Burns, A. L. (1990). Genomic organisation and chromosomal location of the human nucleolin gene. J. Biol. Chem. 265: 14922-14931.
53. Stapleton, P., Weith, A., Urbanek, P., Kozmik, Z., and Busslinger, M. (1993). Chromosomal location of seven PAX genes and cloning of a novel family member, PAX9. Nature Genet. 3: 292-298.
54. Stoilova, D., Child., A., Stoilov, I., Seghatoleslami, R., Crick, R. P., and Sarfarazi, M. (1995). Genetic linkage study of adult-onset primary open angle glaucoma. Am. J. Hum. Genet. 57(4): p. A326 [Abstract 1895].
55. Thylefors, B., and Negrel, A. D. (1994). The global impact of glaucoma. WHO Bulletin OMS 72: 323-326.
56. Tuck, M. W., and Crick, R. P. (1992). Optometrists referral criteria for suspected glaucoma. Health Trends 24: 153-157.
57. Utah Marker Development Group (1995). A collection of ordered tetranucleotide-repeat markers from the human genome. Am. J. Hum. Genet. 57: 619-628.
58. Vogel, R., Crick, R. P., Newson, R. B., Shipley, M., Blackmore, H., and Bulpitt, C. J. (1990). Association between intraocular pressure and loss of visual field in chronic simple glaucoma. Br. J. Ophthalmol. 74: 3-6.
59. Webb, A. C., Collins, K. L., Auron, P. E., Eddy, R. L., Nakai, H., Byers, M. G., Haley, L. L., Henry, W. M., and Shows, T. B. (1986). Interleukin-1 gene (IL1) assigned to the long arm of human chromosome 2. Lymphokine Res. 5: 77-85.
60. Wiggs, J. L., Haines, J. L., Paglinauan, C., Fine, A., Sporn, C., and Lou, D. (1994). Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees. Genomics 21: 299-303.
61. Wiggs, J. L., DelBono, E. A., Schuman, J. S., Hutchinson, B. T., and Walton, D. S. (1995). Clinical features of five pedigrees genetically linked to the juvenile glaucoma locus on chromosome 1q21-q31. Ophthalmology 102: 1782-1789.
62. Wiggs, J. L., Allingham, R. R., DelBono, E. A., Reardon, M., Terminassian, M., Damji, K. F., Youn, J., Jones, K. H., Pericak-Vance, M. A., and Haines, J. L. (1996). The juvenile glaucoma gene on 21q21-q31 is not associated with primary open angle glaucoma (POAG). Invest. Ophthalmol. Visual Sci. 37(3): p. S456 [Abstract 2071].
63. Wirtz, M. K., Kramer, P. L., Topinka, J. R., Acott, T. S., and Samples, J. R. (1995). The adult-onset POAG gene in a large kindred is distinct from the juvenile glaucoma locus on chromosome 1q. Invest. Ophthalmol. Visual Sci. 36(4): p. S555 [Abstract 2578].