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Journal of Assisted Reproduction and Genetics logoLink to Journal of Assisted Reproduction and Genetics
. 1998 May;15(5):331–337. doi: 10.1023/A:1022560914833

Role of the Ped Gene and Apoptosis Genes in Control of Preimplantation Development

Carol M Warner 1,, Abigail S McElhinny 1, Lizi Wu 1, Carsta Cieluch 1, Xiaoling Ke 1, Wei Cao 1, Chaoyu Tang 1, Ginger E Exley 1
PMCID: PMC3454758  PMID: 9604770

Abstract

Purpose:The properties of the mouse Ped gene and the genes that mediate apoptosis in mediating preimplantation embryonic survival were reviewed.

Methods:Preimplantation mouse oocytes and embryos were evaluated microscopically and biochemically for rate of development, degree of fragmentation, and gene expression to correlate these characteristics with embryo mortality. Biochemical assays included PCR for DNA analysis, RT-PCR for mRNA analysis, immuno-PCR for protein analysis, and TUNEL assay for assessment of apoptosis.

Results:Using the mouse as a model system we have identified a gene that controls the rate of development, the Ped gene. The Ped gene product is a class Ib major histocompatibility complex protein called the Qa-2 antigen. Research to understand the molecular mechanisms of Ped gene action and to identify the human homologue of the Ped gene is under way. We have also shown using the mouse model, that fragmented embryos show the morphological and biochemical characteristics of apoptosis. Genes in the two major gene families that regulate apoptosis, the caspase and Bcl-2 families, are expressed in mouse oocytes and preimplantation embryos.

Conclusions:Preimplantation embryonic survival depends on two major morphological parameters: rate of development and degree of fragmentation. A fast rate of development and a low degree of fragmentation lead to a better chance of producing live offspring. Both rate of development and degree of fragmentation are genetically controlled, the former by the Ped gene and the latter most likely by genes that mediate apoptosis. It seems probable that regulation of apoptosis will prove to be a major mechanism that mediates oocyte and preimplantation embryonic survival.

Keywords: Ped gene, apoptosis genes, mouse, preimplantation development

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REFERENCES

  • 1.Verbanac KM, Warner CM. Role of the major histocompatibility complex in the timing of early mammalian development. In: Glasser SR, Bullock DW, editors. Cellular and Molecular Aspects of Implantation. New York: Plenum Press; 1981. pp. 467–470. [Google Scholar]
  • 2.Warner CM, Cao W, Exley GE, McElhinny AS, Alikani M, Cohen J, Scott RT, Brenner CA: Genetic regulation of egg and embryo survival. Hum Reprod 1998 (in press) [DOI] [PubMed]
  • 3.Xu Y, Jin P, Mellor AL, Warner CM. Identification of the Ped gene at the molecular level: The Q9 MHC class I transgene converts the Ped slow to the Ped fast phenotype. Biol Reprod. 1994;51:695–699. doi: 10.1095/biolreprod51.4.695. [DOI] [PubMed] [Google Scholar]
  • 4.Cai W, Cao W, Wu L, Exley GE, Waneck GL, Karger BL, Warner CM. Sequence and transcription of Qa-2 encoding genes in mouse lymphocytes and blastocysts. Immunogenetics. 1996;45:97–107. doi: 10.1007/s002510050177. [DOI] [PubMed] [Google Scholar]
  • 5.Warner CM, Gollnick SO, Flaherty L, Goldbard SB. Analysis of Qa-2 antigen expression by preimplantation mouse embryos: Possible relationship to the Ped gene product. Biol Reprod. 1987;36:611–616. doi: 10.1095/biolreprod36.3.611. [DOI] [PubMed] [Google Scholar]
  • 6.McElhinny A, Warner CM. Detection of major histocompatibility complex class I antigens on the surface of a single murine blastocyst by immuno-PCR. BioTechniques. 1997;23:660–662. doi: 10.2144/97234bm26. [DOI] [PubMed] [Google Scholar]
  • 7.Tian Z, Xu Y, Warner CM. Removal of Qa-2 antigen alters the Ped gene phenotype of preimplantation mouse embryos. Biol Reprod. 1992;47:271–276. doi: 10.1095/biolreprod47.2.271. [DOI] [PubMed] [Google Scholar]
  • 8.Warner CM: Methods for enhancing or reducing preimplantation embryo survival rates. U.S. Patent Application No. 60/053,499 (pending)
  • 9.Bolton VN, Hawes SM, Taylor CT, Parsons JH. Development of spare human preimplantation embryos in vitro: An analysis of the correlations among gross morphology, cleavage rates, and development to the blastocyst. J Vitro Fert Embryo Transfer. 1989;6:30–35. doi: 10.1007/BF01134578. [DOI] [PubMed] [Google Scholar]
  • 10.Levy T, Goldman JA, Dicker D, Ashkenazi J, Feldberg D. Very early pregnancy wastage in in vitro fertilization and embryo transfer (IVF-ET) J Vitro Fert Embryo Transfer. 1991;8:250–253. doi: 10.1007/BF01139779. [DOI] [PubMed] [Google Scholar]
  • 11.Trounson A, Osborn J. In vitro fertilization and embryo development. In: Trounson A, Gardner DK, editors. Handbook of In Vitro Fertilization. Boca Raton, FL: CRC Press; 1993. pp. 57–84. [Google Scholar]
  • 12.Jurisicova A, Casper RF, MacLusky NJ, Mills GB, Librach CL. HLA-G expression during preimplantation human embryo development. Proc Natl Acad Sci USA. 1996;93:161–165. doi: 10.1073/pnas.93.1.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Jurisicova A, Casper RF, MacLusky NJ, Librach CL. Embryonic human leukocyte antigen-G expression: Possible implication for human preimplantation development. Fertil Steril. 1996;65:997–1002. [PubMed] [Google Scholar]
  • 14.Jacobson MD, Weil M, Raff MC. Role of Ced-3/ICE-family proteases in staurosporine-induced programmed cell death. J Cell Biol. 1996;133:1041–1051. doi: 10.1083/jcb.133.5.1041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Weil M, Jacobson MD, Coles HSR, Davies TJ, Gardner RL, Raff KD, Raff MC. Constitutive expression of the machinery for programmed cell death. J Cell Biol. 1996;133:1053–1059. doi: 10.1083/jcb.133.5.1053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Takase K, Ishikawa M, Hoshiai H. Apoptosis in the degeneration process of unfertilized mouse ova. Tohoku J Exp Med. 1995;175:69–76. doi: 10.1620/tjem.175.69. [DOI] [PubMed] [Google Scholar]
  • 17.Nicholson DW, Thornberry NA. Caspases: killer proteases. TIBS. 1997;22:299–306. doi: 10.1016/s0968-0004(97)01085-2. [DOI] [PubMed] [Google Scholar]
  • 18.Reed JC. Double identity for proteins of the Bcl-2 family. Nature. 1997;387:773–776. doi: 10.1038/42867. [DOI] [PubMed] [Google Scholar]
  • 19.Munne S, Alikani M, Tonkin G, Grifo J, Cohen J. Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities. Fertil Steril. 1995;64:382–391. [PubMed] [Google Scholar]

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