Mapping of the genes encoding mouse prostaglandin D, E, and F and prostacyclin receptors

Genomics

Volumn 32, Issue 2, 1996, Pages 285-288

  Ishikawa, Tomo O ^a   Tamai, Yoshitaka ^a   Rochelle, Julie M ^c   Hirata, Masakazu ^b   Namba, Tsunehisa ^b   Sugimoto, Yukihiko ^b   Ichikawa, Atsushi ^b   Narumiya, Shuh ^b   Taketo, Makoto M ^a   Seldin, Michael F ^c  

^a TAIHO PHARMACEUTICAL CO LTD   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL SURFACE RECEPTOR; PROSTACYCLIN RECEPTOR; PROSTAGLANDIN D; PROSTAGLANDIN E; PROSTAGLANDIN F; PROSTAGLANDIN RECEPTOR;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 14; CHROMOSOME 3; CHROMOSOME 7; CHROMOSOME 8; CHROMOSOME ANALYSIS; CHROMOSOME MAP; GENE LOCATION; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; MOUSE; NONHUMAN; PRIORITY JOURNAL;

EID: 17644441130     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0118     Document Type: Article

References (50)

1. 3 prostaglandin receptor. FEBS Lett. 338: 170-174.
2. 2 subtype. J. Biol. Chem. 269: 11873-11877.
3. Belin, D., Vasslli, J.-D., Combepine, C., Godeau, F., Nagamine, Y., Reich, E., Kocher, H. P., and Duvoisin, R. M. (1985). Cloning, nucleotide sequencing and expression of cDNAs encoding mouse urokinase-type plasminogen activator. Eur. J. Biochem. 148: 225-232.
4. Bishop, D. T. (1985). The information content of phase-known matings for ordering genetic loci. Genet. Epidemiol. 2: 349-361.
5. [Ser]Sec gene (Trsp). Mol. Gen. Genet. 248: 247-252.
6. Brilliant, M. H., Williams, R. W., Conti, C. J., Angel, J. M., Oakey, R. J., and Holdener, B. C. (1994). Mouse Chromosome 7. Mamm. Genome 5: S104-S123.
7. Bronson, R. T., Sweet, H. O., Spencer, C. A., and Davisson, M. T. (1992). Genetic and age related models of neurodegeneration in mice: Dystrophic axons. J. Neurogenet. 8: 71-73.
8. Brunet, J. F., Dosseto, M., Denozot, F., Mattei, M. G., Clark, W. R., Haqqi, T. M., Ferrier, P., Nabholz, M., Schmitt-Verhulst, A. M., Luciani, M. F., and Goldstein, P. (1986). The inducible cytotoxic T-lymphocyte-associated gene transcript CTLA-1 sequence and gene localization to mouse chromosome 14. Nature 322: 268-271.
9. Campbell, W. B. (1990). Lipid-derived autacoids: Eicosanoids and platelet-activating factor. In "The Pharmacological Basis of Therapeutics" (A. G. Gilman, T. W. Rall, A. S. Nies, and P. Taylor, Eds.), 8th ed., pp. 600-617, Pergamon Press, New York.
10. Ceci, J. D. (1994). Mouse Chromosome 8. Mamm. Genome 5: S124-S138.
11. Cloudman, M. M., and Bunker, L. E. (1954). The varitint-waddler mouse. J. Hered. 36: 258-263.
12. Coleman, R. A., Kennedy, I., Humphrey, P. P. A., Bunce, K., and Lumley, P. (1990). Prostanoids and their receptors. In "Comprehensive Medicinal Chemistry. The Rational Design, Mechanistic Study and Therapeutic Application of Chemical Compounds" (J. C. Emmet, Ed.), Vol. 3, pp. 634-714, Pergamon Press, New York.
13. Coleman, R. A., Smith, W. L., and Narumiya, S. (1994). International Union of Pharmacology classification of prostanoid receptors: Properties, distribution, and structure of the receptors and their subtypes. Pharmacol. Rev. 46: 205-229.
14. Duncan, A. M. V., Anderson, L. L., Funk, C. D., Abramovitz, M., and Adam, M. (1995). Chromosomal localization of the human prostanoid receptor gene family. Genomics 25: 740-742.
15. Falconer, D. S., Latyszewski, M., and Isaacson, J. H. (1964). Diabetes insipidus associated with oligosyndactylism in the mouse. Genet. Res. 5: 473-488.
16. 1 subtype. J. Biol. Chem. 268: 26767-26772.
17. Gibb, S., Hakensson, E. M., Lundin L.-G., and Shire, J. G. M. (1982). Reduced pigmentation (rp): A new coat colour gene with effects on kidney lysosomal glycosidase in the mouse. Genet. Res. 37: 95-103.
18. Green, E. L. (1981). Linkage, recombination and mapping. In "Genetics and Probability in Animal Breeding Experiments" (E. Green, Ed.), pp. 77-113, MacMillan, New York.
19. Grüneberg, H. (1961). General studies on the skeleton of the mouse. XXIX. Pudgy. Genet. Res. 2: 384-393.
20. 2 receptor. Nature 349: 617-620.
21. Hirata, M., Kakizuka, A., Aizawa, M., Ushikubi, F., and Narumiya, S. (1994). Molecular characterization of a mouse prostaglandin D receptor and functional expression of the cloned gene. Proc. Natl. Acad. Sci. USA 91: 11192-11196.
22. 2 subtype. J. Biol. Chem. 268: 7759-7762.
23. Howard, T. A., Rochelle, J. M., Saunders, A. M., and Seldin, M. F. (1991). A linkage map of mouse chromosome 8: Further definition of the syntenic relationship between mouse chromosome 8 and human chromosomes 8, 16, and 19. Genomics 10: 207-213.
24. Justice, M. J., and Stephenson, D. A. (1994). Mouse Chromosome 13. Mamm. Genome 5: S196-S206.
25. 2 subtype: Cloning, expression and Northern blot analysis. FEBS Lett. 372: 151-156.
26. Lane, P. W., Beamer, T. C., and Myers, D. D. (1976). Myodystrophy, a new myopathy on chromosome 8 of the mouse. J. Hered. 67: 135-138.
27. Lane, P. W., Taylor, B. A., Davisson, M. T., Cook, S., and Rowe, L. (1989). Juvenile bare (jb). Mouse News Lett. 83: 166.
28. Larget-Piet, D., Gerber, S., Bonneau, D., Rozet, J.-M., Maro, S., Ghazi, I., Dufier, J.-L., David, A., Bitoun, P., Weissenbach, J., Munnich, A., and Kaplan, J. (1994). Genetic heterogeneity of Usher syndrome type 1 in French families. Genomics 21: 138-143.
29. Levitt, P., and Noebels, J. L. (1981). Mutant mouse tottering: Selective increase of locus ceruleus axons in a defined single locus mutation. Proc. Natl. Acad. Sci. USA 78: 4630-4634.
30. Lyon, M. F., and Glenister, P. H. (1989). Extra-toes spotting, a new polydactyly mutation. Mouse News Lett. 83: 158-159.
31. 2 receptor: cDNA cloning, expression and Northern blot analysis. Biochem. Biophys. Res. Commun. 184: 1197-1203.
32. Namba, T., Oida, H., Sugimoto, Y., Kakizuka, A., Negishi, M., Ichikawa, A., and Narumiya, S. (1994). cDNA cloning of a mouse prostacyclin receptor. J. Biol. Chem. 269: 9986-9992.
33. 4 subtype. FEBS Lett. 364: 339-341.
34. Ogawa, Y., Tanaka, I., Inoue, M., Yoshitake, Y., Isse, N., Nakagawa, O., Usui, T., Itoh, H., Yoshimasa, T., Narumiya, Y., and Nakao, K. (1995). Structural organization and chromosomal assignment of the human prostacyclin receptor gene. Genomics 27: 142-148.
35. Orn, A., Hakansson, E. M., Gidlund, M., Ramstedt, U., Axberg, I., Wigzell, H., and Lundin, L.-G. (1982). Pigment mutations in the mouse which also affect lysosomal functions lead to suppressed natural killer cell activity. Scand J. Immunol. 15: 305-310.
36. Prins, J.-B., Meister, M. H., and Seldin, M. F. (1994). Mouse Chromosome 3. Mamm. Genome 5: S40-S50.
37. 2 subtype. Mol. Pharmacol. 46: 213-220.
38. Rudert, F., Saunders, A. M., Rebstock, S., Thompson, J. A., and Zimmermann, W. (1992). Characterization of murine carcinoembryonic antigen gene family members. Mamm. Genome 3: 262-273.
39. Samuelson, B., Goldyne, M., Granstorom, E., Hamberg, M., Hammarstrom, S., and Malmsten, C. (1978). Prostaglandins and thromboxanes. Annu. Rev. Biochem. 47: 997-1029.
40. Saunders, A. M., and Seldin, M. F. (1990). A molecular genetic linkage map of mouse chromosome 7. Genomics 8: 525-535.
41. Saunders, A. M., and Seldin, M. F. (1990). The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q. Genomics 6: 324-332.
42. Schaible, R. H. (1961). Stock notes/Notes on mutants. Mouse News Lett. 24: 38-40.
43. 3 subtype. J. Biol. Chem. 267: 6463-6466.
44. Sugimoto, Y., Hasumoto, K., Namba, T., Irie, A., Katsuyama, M., Negishi, M., Kakizuka, A., Narumiya, S., and Ichikawa, A. (1994). Cloning and expression of a cDNA for mouse prostaglandin F receptor. J. Biol. Chem. 269: 1356-1360.
45. 3. Genomics 19: 585-588.
46. Ushikubi, F., Hirata, M., and Narumiya, S. (1995). Molecular biology of prostanoid receptors; an overview. J. Lipid Mediators 12: 343-359.
47. van Abeelen, J. H. F., and van der Kroon, P. H. W. (1967). Nijmegen waltzer - A new biological mutant in the mouse. Genet. Res. 10: 117-118.
48. 1 subtype of prostaglandin E receptor. J. Biol. Chem. 268: 20175-20178.
49. Watson, M. L., D'Eustachio, P. D., Mock, B. A., Steinberg, A. D., Morse, H. C. III, Oakey, R. J., Howard, T. A., Rochelle, J. M., and Seldin, M. F. (1992). A linkage map of mouse chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation. Mamm. Genome 2: 158-171.
50. Zabel, B. U., Eddy, R. L., Lalley, P. A., Scott, J., Bell, G. I., and Shows, T. B. (1985). Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the β subunit of nerve growth factor. Proc. Natl. Acad. Sci. USA 82: 469-473.