Genetic diagnosis of band 3 deficiency and sexing in bovine preimplantation embryos

Journal of Veterinary Medical Science

Volumn 68, Issue 4, 2006, Pages 319-323

  Kageyama, Soichi ^a   Hirayama, Hiroki ^a   Moriyasu, Satoru ^a   Inaba, Mutsumi ^b   Ito, Daisuke ^b   Ohta, Hiroshi ^b   Sawai, Ken ^a   Minamihashi, Akira ^a   Onoe, Sadao ^a  

^a Hokkaido Animal Research Center   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Band 3 deficiency; Cattle; Embryo; Genetic diagnosis; Sexing

Indexed keywords

ERYTHROCYTE BAND 3 PROTEIN;

ANIMAL; ANIMAL DISEASE; ARTICLE; BLASTOCYST; CATTLE; CATTLE DISEASE; EMBRYO TRANSFER; ERYTHROCYTE; FEMALE; GENETICS; GENOTYPE; HEMOLYTIC ANEMIA; HEREDITARY SPHEROCYTOSIS; MALE; METABOLISM; MUTATION; PRENATAL DEVELOPMENT; SEX DETERMINATION;

ANEMIA, HEMOLYTIC; ANIMALS; ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; BLASTOCYST; CATTLE; CATTLE DISEASES; EMBRYO TRANSFER; ERYTHROCYTES; FEMALE; GENOTYPE; MALE; MUTATION; SEX DETERMINATION (ANALYSIS); SPHEROCYTOSIS, HEREDITARY;

ANIMALIA; BOS TAURUS; BOVINAE;

EID: 33646493000     PISSN: 09167250     EISSN: 13477439     Source Type: Journal    
DOI: 10.1292/jvms.68.319     Document Type: Article

References (15)

1. Appa Rao, K.B. and Totey, S.M. 1999. Cloning and sequencing of buffalo male-specific repetitive DNA: sexing of in-vitro developed buffalo embryos using multiplex and nested polymerase chain reaction. Theriogenology 51: 785-797.
2. Ban, A., Sakai, J., Koya, M., Watanabe, D., Abe, S., Abe, S., Itagaki, M., Hoshi, M. and Inaba, M. 1999. Genetic control of red cell band 3 deficiency in Japanese black cattle. J. Jpn. Vet. Med Assoc. 52: 85-89.
3. Chrenek, P., Boulanger, L., Heyman, Y., Uhrin, P., Laurincik, J., Bulla, J. and Renard, J.P. 2001. Sexing and multiple genotype analysis from a single cell of bovine embryo. Theriogenology 55: 1071-1081.
4. Garcia, J.F. 2001. Practical considerations of embryo manipulation: preimplantation genetic typing. Theriogenology 56: 1393-1399.
5. Hirayama, H., Kageyama, S., Moriyasu, S., Hirano, T., Sugimoto, Y., Kobayashi, N., Inaba, M., Sawai, K., Onoe, S. and Minamihashi, A. 2004. Genetic diagnosis of claudin-16 deficiency and sex determination in bovine preimplantation embryos. J. Reprod. Dev. 50: 613-618.
6. Hoeschele, I. and Meinert, T.R. 1990. Association of genetic defects with yield and type traits: the weaver locus effect on yield. J. Dairy Sci. 73: 2503-2515.
7. Inaba, M., Yawata, A., Koshino, I., Sato, K., Takeuchi, M., Takakuwa, Y., Manno, S., Yawata, Y., Kanzaki, A., Sakai, J., Ban, A., Ono, K. and Maede, Y. 1996. Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation. J. Clin. Invest. 97: 1804-1817.
8. Inaba, M. 2000. Chapter 156: Red blood cell membrane defects. pp. 1012-1019. In: Schalm's Veterinary Hematology, 5th ed. (Feldman, R.F., Zinkl, J.G. and Jain, N.C. eds.), Lippincott Williams and Wilkins, New York.
9. Kageyama, S., Yoshida, I., Kawakura, K. and Chikuni, K. 2004. A novel repeated sequence located on the bovine Y chromosome: its application to rapid and precise embryo sexing by PCR. J. Vet. Med. Sci. 66: 509-514.
10. Kobayashi, N., Hirano, T., Ibi, T., Ohtani, T. and Sugimoto, Y. 2002. Association analysis between the deletion mutant allele of claudin-16 deficiency and carcass traits in Japanese black cattle. Nihon Chikusan Gakkaiho 73: 19-23.
11. Niemann, H. Cryopreservation of ova and embryos from livestock: current status and research needs. Theriogenology 35: 109-124.
12. Liu, S.C., Jarolim, P., Rubin, H.L., Palek, J., Amato, D., Hassan, K., Zaik, M. and Sapak, P. 1994. The homozygous state for the band 3 protein mutation in Southeast Asian Ovalocytosis may be lethal. Blood 84: 3590-3591.
13. Schofield, A.E., Reardon, D.M. and Tanner, M.J. 1992. Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells. Nature (Lond.) 355: 836-838.
14. Tanner, M.J. 1993. Molecular and cellular biology of the erythrocyte anion exchanger (AE1). Semin. Hematol. 30: 34-57.
15. Tse, W.T. and Lux, S.E. 2001. Hereditary spherocytosis and hereditary elliptocytosis. pp. 4665-4727. In: The metabolic & Molecular Bases of Inherited Diseases, 8th ed. (C.R. Scriver, Beaudet, A.L., Sly, W.S. and Valle, D., eds.), McGraw-Hill, New York.