Effect of donor cell type on developmental competence, quality, gene expression, and epigenetic status of interspecies cloned embryos produced using cells from wild buffalo and oocytes from domestic buffalo

Theriogenology

Volumn 84, Issue 1, 2015, Pages 101-108.e1

  Saini, M ^a,b   Selokar, N L ^b   Raja, A K ^a   Sahare, A A ^a   Singla, S K ^a   Chauhan, M S ^a   Manik, R S ^a   Palta, P ^a  

^a NATIONAL DAIRY RESEARCH INSTITUTE   (India)

^b CENTRAL INSTITUTE FOR RESEARCH ON BUFFALOES   (India)

Author keywords

Embryo; Epigenetic; Interspecies nuclear transfer; Wild buffalo

Indexed keywords

BUBALUS BUBALIS;

HISTONE;

ANIMAL; BUFFALO; CELL LINEAGE; CELL NUCLEUS TRANSPLANTATION; CLONING; CYTOLOGY; EMBRYO DEVELOPMENT; GENE EXPRESSION REGULATION; GENETIC EPIGENESIS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; OOCYTE; PROCEDURES;

ANIMALS; BUFFALOES; CELL LINEAGE; CLONING, ORGANISM; EMBRYONIC DEVELOPMENT; EPIGENESIS, GENETIC; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HISTONES; NUCLEAR TRANSFER TECHNIQUES; OOCYTES;

EID: 84929966142     PISSN: 0093691X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.theriogenology.2015.02.018     Document Type: Article

References (30)

1. Hedges S, Sagar Baral H, Timmins RJ, Duckworth JW. Bubalus arnee. In: The IUCN Red List of threatened species. Version 2014.3. Accessed on October 2013. http://www.iucnredlist.org.
2. Dominko T., Mitalipova M., Haley B., Beyhan Z., Memili E., McKusick B., et al. Bovine oocyte cytoplasm supports development of embryos produced by nuclear transfer of somatic cell nuclei from various mammalian species. Biol Reprod 1999, 60:1496-1502.
3. Lanza R.P., Cibelli J.B., Diaz F., Moraes C.T., Farin P.W., Farin C.E., et al. Cloning of an endangered species (Bos gaurus) using interspecies nuclear transfer. Cloning 2000, 2:79-90.
4. Loi P., Ptak G., Barboni B., Fulka J., Cappai P., Clinton M. Genetic rescue of an endangered mammal by cross-species nuclear transfer using post-mortem somatic cells. Nat Biotechnol 2001, 19:962-964.
5. Kim M.K., Jang G., Oh H.J., Yuda F., Kim H.J., Hwang W.S., et al. Endangered wolves cloned from adult somatic cells. Cloning Stem Cells 2007, 9:130-137.
6. Oh H.J., Kim M.K., Jang G., Kim H.J., Hong S.G., Park J.E., et al. Cloning endangered gray wolves (Canis lupus) from somatic cells collected postmortem. Theriogenology 2008, 70:638-647.
7. Gomez M.C., Pope C.E., Giraldo A., Lyons L.A., Harris R.F., King A.L., et al. Birth of African wildcat cloned kittens born from domestic cats. Cloning Stem Cells 2004, 6:247-258.
8. Folch J., Cocero M.J., Chesné P., Alabart J.L., Domínguez V., Cognié Y., et al. First birth of an animal from an extinct subspecies (Capra pyrenaica pyrenaica) by cloning. Theriogenology 2009, 71:1026-1034.
9. Campbell K.H.S., Fisher P., Chen W.C., Choi I., Kelly R.D., Lee J.H., et al. Somatic cell nuclear transfer: past, present and future perspectives. Theriogenology 2007, 68:S214-S231.
10. Selokar N.L., George A., Saha A.P., Sharma R., Muzaffer M., Shah R.A., et al. Production of interspecies handmade cloned embryos by nuclear transfer of cattle, goat and rat fibroblasts to buffalo (Bubalus bubalis) oocytes. Anim Reprod Sci 2011, 123:279-282.
11. Priya D., Selokar N.L., Raja A.K., Saini M., Sahare A.A., Nala N., et al. Production of wild buffalo (Bubalus arnee) embryos by interspecies somatic cell nuclear transfer using domestic buffalo (Bubalus bubalis) oocytes. Reprod Domest Anim 2014, 49:343-351.
12. Selokar N.L., Saini M., Muzaffar M., Krishnakanth G., Saha A.P., Chauhan M.S., et al. Roscovitine treatment improves synchronization of donor cell cycle in G0/G1 stage and invitro development of handmade cloned buffalo (Bubalus bubalis) embryos. Cell Reprogram 2012, 14:146-154.
13. Selokar N.L., Shah R.A., Saha A.P., Muzaffar M., Saini M., Chauhan M.S., et al. Effect of post-fusion holding time, orientation and position of somatic cell-cytoplasts during electrofusion on the development of handmade cloned embryos in buffalo (Bubalus bubalis). Theriogenology 2012, 78:930-936.
14. Selokar N.L., Saini M., Palta P., Chauhan M.S., Manik R., Singla S.K. Hope for restoration of dead valuable bulls through cloning using donor somatic cells isolated from cryopreserved semen. PLoS One 2014, 10:e90755.
15. Saini M., Selokar N.L., Agrawal H., Singla S.K., Chauhan M.S., Manik R.S., et al. Treatment of buffalo (Bubalus bubalis) donor cells with trichostatin A and 5-aza-2'-deoxycytidine alters their growth characteristics, gene expression and epigenetic status and improves the invitro developmental competence, quality and epigenetic status of cloned embryos. Reprod Fertil Dev 2014, 10.1071/RD14176.
16. Panarace M., Agüero J.I., Garrote M., Jauregui G., Segovia A., Cané L., et al. How healthy are clones and their progeny: 5 years of field experience. Theriogenology 2007, 67:142-151.
17. Oback B., Wells D. Donor cells for nuclear cloning: many are called, but few are chosen. Cloning Stem Cells 2002, 4:147-168.
18. Strutz F., Okada H., Lo C.W., Danoff T., Carone R.L., Tomaszewski J.E., et al. Identification and characterization of a fibroblast marker: FSP1. J Cell Biol 1995, 130:393-405.
19. Li E. Chromatin modification and epigenetic reprogramming in mammalian development. Nat Rev Genet 2002, 3:662-673.
20. Bestor T.H. The DNA methyltransferases of mammals. Hum Mol Genet 2000, 9:2395-2402.
21. Niemann H., Tian X.C., King W.A., Lee R.S. Epigenetic reprogramming in embryonic and foetal development upon somatic cell nuclear transfer cloning. Reproduction 2008, 135:151-163.
22. Jenuwein T., Allis C.D. Translating the histone code. Science 2001, 293:1074-1080.
23. Danial N.N., Korsmeyer S.J. Cell death: critical control points. Cell 2004, 116:205-219.
24. Jang G., Jeon H.Y., Ko K.H., Park H.J., Kang S.K., Lee B.C., et al. Developmental competence and gene expression in preimplantation bovine embryos derived from somatic cell nuclear transfer using different donor cells. Zygote 2005, 13:187-195.
25. Nichols J., Zevnik B., Anastassiadis K., Niwa H., Klewe-Nebenius D., Chambers I., et al. Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4. Cell 1998, 95:379-391.
26. Reima I., Lehtonen E., Virtanen I., Flechon J. The cytoskeleton and associated proteins during cleavage, compaction and blastocyst differentiation in the pig. Differentiation 1993, 54:35-45.
27. Saadeldin I.M., Choi W., Roibas Da, Torre B., Kim B., Lee B., et al. Embryonic development and implantation related gene expression of oocyte reconstructed with bovine trophoblast cells. J Reprod Dev 2012, 58:425-431.
28. Kim M.S., Sakurai T., Bai H., Bai R., Sato D., Nagaoka K., et al. Presence of transcription factor OCT4 limits interferon-tau expression during the pre-attachment period in sheep. Asian-Australas J Anim Sci 2013, 26:638-645.
29. Bazer F., Spencer T., Ott T. Interferon tau: a novel pregnancy recognition signal. Am J Reprod Immunol 1997, 37:412-420.
30. Hochedlinger K., Jaenisch R. Nuclear reprogramming and pluripotency. Nature 2006, 441:1061-1067.