Localization of the locus causing Spider Lamb Syndrome to the distal end of ovine Chromosome 6

Mammalian Genome

Volumn 10, Issue 1, 1999, Pages 35-38

  Cockett, N E ^a   Shay, T L ^a   Beever, J E ^b   Nielsen, D ^c   Albretsen, J ^d   Georges, M ^e   Peterson, K ^a   Stephens, A ^a   Vernon, W ^a   Timofeevskaia, O ^a   South, S ^a   Mork, J ^a   Maciulis, A ^a   Bunch, T D ^a  

^a UTAH STATE UNIVERSITY   (United States)

^b UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^c NORTH CAROLINA STATE UNIVERSITY   (United States)

^d ASPCA ANIMAL POISON CONTROL CENTER   (United States)

^e UNIVERSITY OF LIÈGE   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; AUTOSOMAL INHERITANCE; CATTLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 6; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; LAMB; NONHUMAN; SHEEP; SYNDROME; TELOMERE;

ANIMAL DISEASES; ANIMALS; CHROMOSOME MAPPING; FEMALE; GENETIC MARKERS; INBREEDING; LINKAGE (GENETICS); MALE; OSTEOCHONDRODYSPLASIAS; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3; RECEPTORS, FIBROBLAST GROWTH FACTOR; SHEEP;

ANIMALIA; ARANEAE; BOS TAURUS; MAMMALIA; OVIS; OVIS ARIES;

EID: 0032768474     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900938     Document Type: Article

References (38)

1. Beever JE, Fisher SR, Lewin HA (1997) Polymorphism identification in the ACADM, AT3 IL10, MYOG and TSHB genes of cattle. Anim Genet 28, 373-374
2. Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, et al. (1995) A recurrent mutation in the tyrosine kinase domain of fibroblast growth receptor 3 causes hypochondroplasia. Nat Genet 10, 357-359
3. Berg PT, Alstad AD, Moore BL, Vanek JA, Berg IE, et al. (1987) The mode of inheritance of the Spider Lamb Syndrome in Suffolk sheep. SID Res Digest 4, 1-3
4. Bishop MD, Kappes SM, Keele JW, Stone RT, Sunden SLF, et al. (1994) A genetic linkage map for cattle. Genetics 136, 619-639
5. Colvin JS, Bohne BA, Harding GW, McEwen DG, Ornitz DM (1996) Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. Nat Genet 12, 390-397
6. Cottingham Jr RW, Idury RM, Schdffer AA (1994) Faster sequential genetic linkage computations. Am J Hum Genet 53, 252-263
7. Crawford AM, Dodds KG, Ede AJ, Pierson CA, Montgomery GW, et al. (1995) An autosomal genetic linkage map of the sheep genome. Genetics 140, 703-724
8. Deng C, Wynshaw-Boris A, Zhou F, Kuo A, Leder P (1996) Fibroblast growth factor receptor 3 is a negative regulator of bone growth. Cell 84, 911-921
9. Green P, Falls K, Crooks S (1990) Documentation for CRI-MAP, version 2.4. (St. Louis: Washington University School of Medicine)
10. Gusella JF, Tanzi RE, Bader PI, Phelan MC, Stevenson R, et al. (1985) Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome. Nature 318, 75-78
11. Hollway GE, Phillips HA, Ades LC, Haan EA, Mulley JC (1995) Localisation of craniosynostosis Adelaide type to 4p16. Hum Mol Genet 4, 681-683
12. Hulme DJ, Smith AJ, Silk JP, Redwin JM, Beh KJ (1995) Polymorphic sheep microsatellites at the McM2, McM131, McM135, McM136, McM140, McM200, McM214, McM373, McM505, McM507 and McM512 loci. Anim Genet 26, 369-370
13. Kappes SM, Keele JW, Stone RT, McGraw RA, Sonstegard TS, et al. (1997) A second generation linkage map of the bovine genome. Genome Res 7, 235-249
14. Keegan K, Johnson DE, Williams LT, Hayman MJ (1991) Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3. Proc Natl Acad Sci USA 88, 1095-1099
15. Lathrop GM, Lalouel JM, Julier C, Ott J (1984) Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 101, 3443-3446
16. Lord EA, Penty JM, Dodds KG, Henry HM, Crawford AM, et al. (1996) The linkage map of sheep chromosome 6 compared with orthologous regions in other species. Mamm Genome 7, 373-376
17. Lumsden JM, Lord EA, Montgomery GW (1996) Characterization and linkage mapping of ten sheep microsatellite markers derived from a sheep x hamster cell hybrid. Anim Genet 27, 203-206
18. Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16, 1215
19. Partington MW, Fagan K, Soubjaki V, Turner G (1997) Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome. J Med Genet 34, 719-728
20. Phillips PH, Bunn CM, Anderson CE (1993) Ovine hereditary chondrodysplasia (spider syndrome) in Suffolk lambs. Aust Vet J 70, 73-74
21. Polymeropoulos MH, Ide SE, Wright M, Goodship J, Weissenbach J, et al. (1996) The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16. Genomics 35, 1-5
22. Rook JS, Kopcha M, Spaulding K, Coe P, Benson M, (1988) Diagnosis of hereditary chondrodysplasia (spider lamb syndrome) in sheep. J Am Vet Med Assoc 188, 713-718
23. Saperstein G, Leipold HW, Dennis SM (1975) Congenital defects of sheep. J Am Vet Med Assoc 167, 314-322
24. Schdffer AA, Gupta SK, Shriram K, Cottingham Jr RW (1994) Avoiding recomputation in linkage analysis. Hum Hered 44, 225-237
25. Shiang R, Thompson LM, Zhu Y-Z, Church DM, Fielder TJ, et al. (1994) Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78, 335-342
26. Tavormina PL, Shiang T, Thompson LM, Zhu Y-Z, Wilkin DJ, et al. (1995) Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nat Genet 9, 321-328
27. Teres V, Lester DH, Williams JL (1996) Mapping of bovine fibroblast growth factor receptor 3 (FGFR3) to the telomeric region of chromosome 6 by SSCP analysis. Anim Genet 27, 371
28. Thomas DL, Cobb AR, Waldron DF (1988) Spider syndrome - a genetic defect found in American Suffolk sheep. Proc Third World Congress on Sheep and Beef Cattle Breeding 1, 649-651
29. Thompson LM, Plummer S, Schalling M, Altherr MR, Gusella JF, et al. (1991) A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4. Genomics 11, 1133-1142
30. Troyer DL, Thomas DL, Stein LE (1988) A morphologic and biochemical evaluation of the spider syndrome in Suffolk sheep. Anat Histol Embryol 17, 289-300
31. Vanek JA, Alstad AD, Berg IE, Misek AR (1986) Spider syndrome in lambs: a clinical and postmortem analysis. Vet Med 81, 663-668
32. Vanek JA, Walter PA, Alstad AD (1987) Comparing spider syndrome in Hampshire and Suffolk sheep. Food-Anim Prac 82, 430-437
33. Vanek JA, Bleier WJ, Whited DA, Alstad AD (1988) Comparison of G-banded chromosomes from clinically normal lambs and lambs affected with ovine hereditary chondrodysplasia (spider syndrome). Am J Vet Res 49, 1164-1168
34. Vanek JA, Walters PA, Alstad AD (1989) Radiographic diagnosis of hereditary chondrodysplasia in newborn lambs. J Am Vet Med Assoc 194, 244-248
35. Wang CT, Dickerson GE (1991) Simulated effects of reproductive performance on life-cycle efficiency of lamb and wool production at three lambing intervals. J Anim Sci 69, 4338-4347
36. Weber B, Reiss O, Hutchinson G, Collins C, Lin BY, Kowbel D, Andrew S, Schappert K, Hayden MR (1991) Genomic organisation and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localization to 4p16.3. Nucleic Acids Res 19, 6263-6268
37. Webster MK, Donoghue DJ (1997) FGFR activation in skeletal disorders: too much of a good thing. Trends Genet 13, 178-182
38. Womack JE, Kata SR (1995) Bovine genome mapping: evolutionary inference and the power of comparative genomics. Curr Opin Genet Dev 5, 725-733