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2002 | 49 | 4 |

Tytuł artykułu

Genetyczne podloze niektorych chorob koni

Treść / Zawartość

Warianty tytułu

Języki publikacji

PL

Abstrakty

EN
Recently recognized genetical background of a few disease unit in the horses was reviewed in presented paper. The identification of these disorders was possible to great extent due to the improvement had been done in studies on equine gene mapping. A molecular basis of the following diseases were discussed: hypercalaemic periodic paralysis (HYPP), severe combined immunodeficiency (SCID) and overo lethal white syndrome (OLWS). Preliminary studies on the reasons of such disorders like: exertional rhabdomyolisis (ER), summer dermatitis and chronic obstructive pulmonary disease (COPD) were also presented.

Wydawca

-

Rocznik

Tom

49

Numer

4

Opis fizyczny

s.155-164,bibliogr.

Twórcy

  • Instytut Genetyki i Hodowli Zwierzat PAN, Jastrzebiec, 05-551 Mrokow
autor

Bibliografia

  • [1] Amiel J., Attie T., Jan D., Pelet A., Edery P. 1996. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschprung disease. Hum. Mol. Genet. 5: 355-357.
  • [2] Auricchio A., Casari G., Staiano A., Ballabio A. 1996. Endothelin-B receptor mutations in patients with isolated Hirschprung disease from non-inbred population. Hum. Mol. Genet. 5: 351-354.
  • [3] Badner J.A., Sieber W.K., Garver K.L., Chakravarti A. 1990. A genetic study of Hirschprung disease. Amer. J. Hum. Genet. 46: 568-580.
  • [4] Bailey E., Binns M.M. 1998. The horse gene map. ILAR J. 39: 171-176.
  • [5] Bailey E., Reid R.C., Skow L.C., Mathiason K., Lear T.L., McGuire T. C.1997. Linkage of the gene for equine combined immunodeficiency disease to mikrosatellite markers HTG8 and HTG4; synteny and FISH mapping to ECA9. Anim. Genet. 28: 268-273.
  • [6] Bernoco D., Bailey E. 1998. Frequency of the SCID gene among Arabian horses in the USA. Anim. Genet. 29: 41-42.
  • [7] Bowling A.T., Byrns G., Spier S. 1996. Evidence for a single pedigree source of the hyperkalemic periodic paralysis susceptibility gene in Quarter horses. Anim. Genet. 27: 279-281.
  • [8] Broström H., Larsson A., Troedsson M. 1987. Allergic dermatitis (sweet itch) of Icelandic horses in Sweden: an epidemiological study. Equine Vet. J. 19: 229-236.
  • [9] Goldberg E.L. 1984. An epidemiological study of Hirschprung's disease. Int. J. Epidemiol. 13: 355-363.
  • [10] Guerin G., Bailey E., Anderson I., Antczak D.F., Bell K., Bernoco D., Binns M.M., Bowlind A.T., Brandon R., Cholewiński G., Cothran E.G., Ellegren H., Forster M., Godard S., Horin P., Ketchum M., Lindgren G., McPartlan H., Meriaux J.C., Mickelson J., Millon L.V., Neau A., Roed K.H., Sandberg K., Skow L., Stott M., Swinburne J., Van Haeringen H., Van Haeringen W.A., Ziegle J. 1998. Report of the International Equine Gene Mapping Workshop: First linkage map. Anim. Genet. 29 (Suppl. 1): 42.
  • [11] Guerin G., Bailey E., Bernoco D., Anderson I., Antczak D.F., Bell K., Binns M.M., Bowling A.T., Brandon R., Cholewiński G., Cothran E.G., Ellegren H., Forster M., Godard S., Horin P., Ketchum M., Lindgren G., McPartlan H., Meriaux J.C., Mickelson J.R., Millon L.V., Murray J., Neau A., Roed K., Sandberg K., Shiue Y.L., Skow L.C., Stott M., Swinburne S., Valberg J., Van Haeringen H., Van Haeringen W.A., Ziegle J. 1999. Report of the International Equine Gene Mapping Workshop: Male linkage map. Anim. Genet. 30: 341-354.
  • [12] Jeffcott L.B. 1996. Osteochondrosis - an international problem for the horse industry. J. Equine Vet. Sci. 16: 32-37.
  • [13] Lazary S., Marti E., Szalai G., Gaillard C., Gerber H. 1994. Studies on the frequency and assotiation of equine leucocyte antigens in sarcoid and summer dermatitis. Anim. Genet. 25 (Suppl. 1): 75-80.
  • [14] Lindgren G., Sandberg K., Persson H., Marklund S., Breen M., Sandgren B., Carlsten J., Ellegren H. 1998. A primary male autosomal linkage map of the horse genome. Genome Res. 8: 951-966.
  • [15] Marti E., Gerber H., Essich G., Oulehla J., Lazary S. 1991. The genetic basis of equine allergic diseases I. Chronic hypersensitivity bronchitis. Equine Vet. J. 23: 457-460.
  • [16] Marti E., Gerber H., Lazary S. 1992. On the genetic basis of equine allergic diseases: II. Insect bite dermal hypersensitivity. Equine Vet. J. 24: 113-117.
  • [17] McCabe L., Griffin L.D., Kinzer A., Chandler M., Beckwith J.B., McCabe R.B. 1990. Overo lethal white foal syndrome: equine model of aganglionic megacolon (Hirschprung disease). Amer. J. Med. Genet. 36: 336-340.
  • [18] McGuire T.C., Poppie M.J., Banks K.L. 1974. Combined (B- and T-lymphocyte) immunodeficiency: a fatal genetic disease in Arabian foals. J. Amer. Vet. Med. Assn. 164: 70-76.
  • [19] Metallinos D.L., Bowling A.T., Rine J. 1998. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Syndrome: an equine version of Hirschprung Disease. Mamm. Genome 9: 426-431.
  • [20] Naylor J.M., Nickel D.D., Trimino G., Card C., Lightfoot K., Adams G. 1999. Hyperkalaemic periodic paralysis in homozygous and heterozygous horses: a co-dominant genetic condition. Equine Vet. J. 2: 153-159.
  • [21] Poppie M.J., McGuire T.C. 1977. Combined immunodeficiency in foals of Arabian breeding: evaluation of mode of inheritance and estimation of prevalence of affected foals and carrier mares and stallions. J. Amer. Vet. Med. Assn. 170: 31-33.
  • [22] Raudsepp T., Frönicke L., Schertan H., Gustavsson I., Chowdhary B.P. 1996. ZOO-FISH delineates conserved chromosomal segments in horse and man. Chromosome Res. 4: 218-225.
  • [23] Rudel R. 1986. The pathophysiologic basis of the myotonias and the periodic paralyses. W: Myology: Basic and Clinical (ed. By A.G. Engel & B.Q. Banker). McGraw-hill, New York: 1297-1311.
  • [24] Rudolph J.A., Spier S.J., Byrns G., Hoffman E.P. 1992. Linkage of hyperkalaemic periodic paralysis in Quarterhorses to the horse adult skeletal muscle sodium channel gene. Anim. Genet. 23: 241-250.
  • [25] Rudolph J.A., Spier S.J., Byrns G., Royas C.V., Bernoco D., Hoffman E.P. 1992. Periodic paralysis in Quarterhorses: a sodium chanel mutation disseminated by selective breeding. Nature Genet. 2: 144-147.
  • [26] Santschi E.M., Purdy A.K., Valberg S.J., Vrotsos P.D., Kaese H., Mickelson J.R. 1998. Endothelin receptor B polymophism associated with lethal white foal syndrome in horses. Mamm. Genome 9: 306-309.
  • [27] Santschi E.M., Vrotsos P.D., Purdy A.K., Mickelson J.R. 2001. Incidence of endothelin receptor B mutation that causes lethal white foal syndrome in white-patterned horses. Amer. J. Vet. Res. 1: 97-103.
  • [28] Schneider L.E., Leipold H.W. 1978. Recessive lethal white in foals. J. Equine Med. Surgery 2: 479-482.
  • [29] Shin E.K., Perryman L.E., Meek K. 1997. A kinase negative mutation of DNA-PKcs in eguine SCID results in defective coding and signal joint formation. J. Immunol. 158: 3565-3569.
  • [30] Spier S.J., Carlson G.P., Holliday T.A., Cardinet III G.H., Pickar J.G. 1990. Hypercalemic periodic paralysis in horses. J. Amer. Vet. Med. Assn. 197: 1009-1017.
  • [31] Spier S.J., Carlson G.P., Harrold D., Bowling A., Byms G., Bemoco D. 1993. Genetic study of hypercalemic periodic paralysis in horses. J. Amer. Vet. Med. Assn. 202: 933-937.
  • [32] Steiss J.E., Naylor J.M. 1986. Episodic muscle tremors in a Quater Horse: resemblance to hypercalemic periodic paralysis. Can. Vet. J. 27: 332-335.
  • [33] Terry R.R., Cholewiński G., Cothran E.G. 1999. Absence of the severe combined immunodeficiency disease gene among Arabian horses in Poland. J. Appl. Genet. 1: 39-41.
  • [34] Trommershausen-Smith A. 1977. Lethal White foals in matings of overo spotted horses. Theriogenology 8: 303-311.
  • [35] Valberg S.J., Mickelson J.R., Gallant E.M.1999. Genetic studies of equine myopathies. Plant and Animal Genome VII Conference, San Diego,USA, 17-21.01.1999.
  • [36] Valberg S., Mickelson J., Gallant E., de La Corte F., Ward T. 2001. Investigating Heritable Myopathies in the Horse. 4th International Equine Gene Mapping Workshop, Brisbane, Australia, 4-6.06.2001.
  • [37] Wiler R., Leber R., Moore B.B., VanDyk L., Perryman L.E., Meek K.D. 1995. Equine severe combined immunodeficiency: a defect in V(D)J recombination and DNA-dependent protein kinase activity. Proc. Nat. Acad. Sci. USA 92: 11485-11489.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-5377f986-8822-4395-9898-db88c449d651
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