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Autosomal Trisomy in a Heifer
Autosomal trisomi hos en kviga
Acta Veterinaria Scandinavica volume 28, pages 1–8 (1987)
Abstract
A malformed Ayrshire heifer had one additional autosome in all the lymphocyte metaphases studied. Chromosome banding techniques showed the karyotype of the calf to be 2n = 61, XX, +24.
Slight prognathia of the lower jaw and peculiar abbrevations in the structure of the genitals were the most apparent anomalies, in addition to heart abnormalities, a poorly-closed urachus and slow growth rate.
Sammanfattning
Hos en Ayrshire-kviga med långsam tillväxt och plötslig död i en ålder av 1 år kunde en extra autosomal kromosom påvisas i alla lymfocyter. Bandfärgning av kromosomerna visade karyotypen vara 2n = 61, XX, +24.
Kvigan hade en lindrig prognathia inferior, ett litet navelbrock samt utvecklingsstörningar i urogenitalsystemet och defekter i hjärtat.
References
Alberman E, Creasy MR: Frequency of chromosomal abnormalities in miscarriers and perinatal death. J. Med. Genet. 1977, 14, 313–315.
Carr DH: Genetic basis of abortation. Annu. Rev. genet. 1971, 5, 65–80.
Chandley AC: The origin of chromosomal aberrations in man and their potential for survival and reproduction an the adult human population. Ann. Génét. 1981, 24, 5–11.
Di Berardino D, Lannuzzi L: Detailed description of R-banded bovine chromosomes. J. Hered. 1982, 73, 434–4138.
Di Berardino D, Iannuzzi L, Lioi MB: The high-resolution RBA-banding pattern of bovine chromosomes. Cytogenet. Cell Genet. 1985, 39, 136–139.
Dunn HO, Johnson RH Jr: A 61 XY cell line in a calf with extreme brachygnathia. J. Dairy Sei. 1972, 55, 524–526.
Dutrillaux B, Laurent C, Couturier J, Lejeune J: Coloration des chromosomes humains par 1’acridine orange après traitement par le 5 bromodeoxyuridine. (Acridine orange staining method in human chromosomes treated with 5 bromodeoxyuridine). C. R. Acad. Sc. (Paris) 1973, 276, 3179–3181.
Ettala E, Ruohomäki H: Lypsykaijan pitkäaikaiskoe: Erirotuisten hiehojen kasvatulokset. (The growth rate in female calf of different breed). Maaseudun Tulevaisuus, Koetoiminta ja Käytänto 16.12.1980.
Fechheimer NS: Cytogenetics in animal production. J. Dairy Sei. 1979, 62, 844–853.
Gluhovschi N, Bistriceanu M: Untersuchungen zur Chromosomenpathologie in der Veterinärmedizin. (Veterinary medicine and cytogenetics). 1. europäisches Kolloquium über Zytogenetik in Veterinärmedizin und Säugetierkunde. Giessen 1970, in Giessener beitr. Erbpath. Zuchthyg. Sonderheft. 1970, 1, 93–100.
Gluhovschi N, Bistriceanu M, Palicica R: Les troubles de la reproduction chez les animeaux domestiques dus à des modifications du genome. (Cytogenetic studies of domestic animals with reproductive problems). Cah. Méd. Vét. 1975, 44, 155–163.
Gustavsson I: Chromosome aberrations and their influence on the reproductive performance of domestic animals - a review. Z. Tierzüchtg. Züchtgsbiol. 1980a, 97, 176–195.
Gustavsson I: Banding techniques in chromosome analysis of domestic animals. Adv. Vet. Sci. Comp. Med. 1980b, 24, 245–289.
Gustavsson I, Settergren I, King WA: Occurrence of two different reciprocal translocations in the same litter of domestic pigs. Hereditas 1983, 99, 257–267.
Hare WCD, Singh EL, Betteridge KJ, Eaglesome MD, Randall GCB, Mitchell D, Bilton RJ, Trounson AO: Chromosomal analysis of 159 bovine embryos collected 12 to 18 days after estrus. Can. J. Genet. Cytol. 1980, 22, 615–626.
Herzog A: Autosomale Trisomie bei der letalen Brachygnatie des Rindes (bovines Trisomie- Brachygnathia-syndrom). (Autosomal trisomy in cattle with brachygnathia inferior). Dtsch. Tierärztl. Wschr. 1974, 81, 77–100.
Herzog A, Höhn H: Autosomale Trisomie bei einem Kalb mit Brachygnathia inferior und Ascites congenitus. (Autosomal trisomy in a calf with Brachygnathia inferior and congenital edema). Dtsch. Tierärztl. Wschr. 1968, 75, 604–606.
Herzog A, Höhn H: Autosomale Trisomie bei der letalen Brachygnathie des Rindes. (Autosomal trisomy in cattle with lethal brachygnathia). Cytogenetics 1971, 10, 347–355.
Herzog A, Höhn H, Olyschläger F, Rusch P: 17-Trisomie-Mosaik beim Rind. (17-trisomicmosaic cattle). Berl. Münch. Tierärztl. Wschr. 1982, 95, 352–354.
Herzog A, Höhn H, Rieck GW: Survey of recent situation of chromosome pathology in different breeds of german cattle. Ann. Génét. Sél. Anim. 1977, 9, 471–491.
Höhn H, Herzog A: Zwei weitere Fälle von autosomaler trisomie bei Kälbern mit Brachygnathia inferior und anderen Missbildungen. (Two additional cases of autosomal trisomy in calves with brachygnathia inferior and other anerrations). Giessener Beitr. Erbpath. Zuchthyg. 1970, 3, 1–7.
Jacobs PA, Morton NE: Origin of human trisomies and polyploids. Hum. Hered. 1977, 27, 59–72.
King WA, Linares T, Gustavsson I, Bane A: Presumptive translocation type in embryos sired by bulls heterozygous for the 1/29 translocation. Hereditas 1980, 92, 167–169.
King WA, Linares T, Gustavsson I: Cytogenetics of preimplantation embryos sired by bulls heterozygous for the 1/29 translocation. Hereditas 1981, 94, 219–224.
Lejeune J, Gautier M, Turpin R: Etude des chromosomes somatiques de neuf enfants mongoliens. (Extra somatic chromosome in newborn with mongolism). C. R. Acad. Sci. 1959, 245, 1721–1722.
Lin CC, Newton DR, Church RB: Identification and nomenclature for G-banded bovine chromosomes. Can. J. Genet. Cytol. 1977, 79, 271–282.
Mayr B, Krutzler H, Auer H, Scheieger W, Sasshofer K, Glawischnig E: A viable calf with trisomy 22. Cytogenet. Cell genet. 1985, 39, 77–79.
Mori M, Sasaki M, Makino S, Ishikawa T, Kawata K: Autosomal trisomy in a malformed newborn calf. Proc. Japan Acad. 1969, 45, 955–957.
Popescu CP: Cytogenetic study on embryos sired by a bull carrier of 1/29 translocation. Proc. 4th Eur. Colloq. Cytogenet. Dornest. Anim., Uppsala 1980, pp. 182–186.
Proceedings of the First International Conference for the Standardization of Banded Karyotypes of Domestic Animals. Reading, England. 1976. (Eds. Ford CE, Pollock DL & Gustavsson I). Hereditas 1980, 92, 145–162.
Rieck GW: Veterinary medicine and cytogenetics. Proc. 6th Eur. Colloq. Cytogenet. Dornest. Anim., Zürich 1984, pp. 20–34.
Seabright M: A rapid banding technique for human chromosomes. Lancet 1971, 2, 971–972.
Sumner AT: A simple technique for demonstrating centrometric heterochromatin. Exp. Cell. Res. 1072, 75, 304–306.
Tschudi P, Ueltschi G, Martiq J, Küpfer U: Autosomale Trisomie als Ursache eines hohen Ventrikel-septumdefekts bei einem Kalb der Simmentalerrasse. (Autosomal trisomy as the cause for defects of the interventricular septum in a Simmental calf). Schweiz. Arch. Tierheilkd. 1975, 777, 335–340.
Tschudi P, Zahner B, Küpfer U, Stämpfli G: Chromosomenuntersuchungen an schweizerischen Rindermassen. (Chromosome investigation of Brown Swiss cattle). Schweiz. Arch. Tierheilkd. 1977, 119, 329–336.
Acknowledgements
We are grateful to veterinarian Eero Remes for his kind cooperation in referring the calf of the present study. We would also like to thank Tarja Väisänen for her excellent laboratory assistance, Dr. Henni Höhn for her interest in this study and Drs. Ingemar Gustavsson and Dino di Berardino for their comments on the karyotype.
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Mäkinen, A., Alitalo, I. & Alanko, M. Autosomal Trisomy in a Heifer. Acta Vet Scand 28, 1–8 (1987). https://doi.org/10.1186/BF03548250
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DOI: https://doi.org/10.1186/BF03548250