Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18

Investigative Ophthalmology and Visual Science

Volumn 48, Issue 8, 2007, Pages 3506-3515

  Tetens, Jens ^a   Ganter, Martin ^a   Müller, Gundi ^a   Drogemüller, Cord ^a,b  

^a UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

^b UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ANOPHTHALMIA; ANTERIOR EYE CHAMBER; ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME; CHROMOSOME 18; CHROMOSOME 23; CHROMOSOME BREAKAGE; GENE; GENE LOCATION; GENE MUTATION; GENETIC LINKAGE; GENOME; GENOTYPE; HAPLOTYPE; HISTOLOGY; LAMB; LENS; MATING; MICROPHTHALMIA; MOUSE; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PHENOTYPE; PRIORITY JOURNAL; TGIF1 GENE; VITREOUS BODY; ANIMAL; CHROMOSOME MAP; DISEASE MODEL; FEMALE; GENETICS; HUMAN; MALE; PATHOLOGY; PEDIGREE; SHEEP;

HOMEODOMAIN PROTEIN; MICROSATELLITE DNA; REPRESSOR PROTEIN; TGIF1 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ANIMALS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, MAMMALIAN; DISEASE MODELS, ANIMAL; FEMALE; HAPLOTYPES; HOMEODOMAIN PROTEINS; HUMANS; LINKAGE (GENETICS); MALE; MICROPHTHALMOS; MICROSATELLITE REPEATS; PEDIGREE; REPRESSOR PROTEINS; SHEEP;

EID: 34648840370     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.07-0041     Document Type: Article

References (22)

1. Graw J. The genetic and molecular basis of congenital eye defects. Nat Rev Genet. 2003;4:876-888.
2. Patterson DF, Haskins ME, Jezyk PF, et al. Research on genetic diseases: reciprocal benefits to animals and man. J Am Vet Med Assoc. 1988;193:1131-1144.
3. de Groot T. Blind geboren lammeren. Landbouwkd Tijdschr. 1957;69:819-822.
4. Hanset R. Microphthalmie hereditaire chez des moutons de race Texel. Ann Med Vétérinaire. 1961;105:443-449.
5. Haring F, Gruhn R. Mikrophthalmie, ein einfach rezessiver Erbfehler beim Schaf. Züchtungskd. 1970;42:385-390.
6. Jackson EKM. Microphthalmia in sheep. Vet Rec. 1990;126:650.
7. Roe WD, West DM, Walshe MT, Jolly RD. Microphthalmia in Texel lambs. NZ Vet J. 2003;51:194-195.
8. van der Linde-Sipman JS, van den Ingh TS, Vellema P. Morphology and morphogenesis of hereditary microphthalmia in Texel sheep. J Comp Pathol. 2003;128:269-275.
9. Tetens J, Bürstel D, Ganter M, et al. Untersuchungen zur kongenitalen Mikrophthalmie beim Texelschaf. Tierärztl Prax. 2007;35:165-172.
10. Labs I. Untersuchungen zur Morphologie der kongenitalen Mikrophthalmie beim Schaf mit Beiträgen zur Átiopathogenese. Dissertation. Giessen, Universität, Veterinärmedizinische Fakultät; 1977.
11. Cockett NE. Current status of the ovine genome map. Cytogenet Genome Res. 2003;102:76-78.
12. Tetens J, Goldammer T, Maddox JF, Cockett NE, Leeb T, Drögemüller C. A radiation hybrid map of sheep chromosome 23 based on ovine BAC end sequences. Anim Genet. 2007;38:132-140.
13. Everts-van der Wind A, Larkin DM, Green CA, et al. A high-resolution whole-genome cattle-human comparative map reveals details of mammalian chromosome evolution. Proc Natl Acad Sci USA. 2005;102:18526-18531.
14. Schibler L, Roig A, Mahe MF, et al. High-resolution comparative mapping among man, cattle and mouse suggests a role for repeat sequences in mammalian genome evolution. BMC Genomics. 2006;7:194.
15. Tammen I, Houweling PJ, Frugier T, et al. A missense mutation (c. 184C→T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA. Biochim Biophys Acta. 2006;1762:898-905.
16. Lander ES, Green P. Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA. 1987;84:2363-2367.
17. Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet. 2002;30:97-101.
18. Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet. 1996;58:1347-1363.
19. Aso S, Horiwaki S, Noda S. Lens aplasia: a new mutation producing lens abnormality in the mouse. Lab Anim Sci. 1995;45:41-46.
20. Gripp KW, Wotton D, Edwards MC, et al. Mutations in TGIF1 cause holoprosencephaly and link NODAL signalling to human neural axis determination. Nat Genet. 2000;25:205-208.
21. Abbasi AR, Ihara N, Watanabe T, et al. Linkage mapping of the locus responsible for congenital multiple ocular defects in cattle on bovine chromosome 18. Mamm Genome. 2005;16:731-737.
22. Abbasi AR, Geriletoya, Ihara N, Khalaj M, Sugimoto Y, Kunieda T. An integrated radiation hybrid map of bovine chromosome 18 that refines a critical region associated with multiple ocular defects in cattle. Anim Genet. 2006;37:58-61.