Abstract

To determine whether chromosomes in the porcine first polar body (PB1) can complete the second meiotic division and subsequently undergo normal pre-implantation embryonic development, we examined the developmental competence of PB1 chromosomes injected into enucleated MII stage oocytes by nuclear transfer method (chromosome replacement group, CR group). After parthenogenetic activation (PA) or in vitro fertilization (IVF), the cleavage rate of reconstructed oocytes in the IVF group (CR-IVF group, 36.4 ± 3.2%) and PA group (CR-PA group, 50.8 ± 4.2%) were significantly lower than that of control groups in which normal MII oocytes were subjected to IVF (MII-IVF group, 75.8 ± 1.5%) and PA (MII-PA group, 86.9 ± 3.7%). Unfertilized rates was significantly higher in the CR-IVF group (48.6 ± 3.3%) than in the MII-IVF group (13.1 ± 3.4%). The blastocyst formation rate was 8.3 ± 1.9% in the CR-PA group, whereas no blastocyst formation was observed in the CR-IVF group. To produce tetraploid parthenogenetic embryos, intact MII stage oocytes injected with PB1chromosomes were electrically stimulated, treated with 7.5 μg/mL cytochalasin B for 3 h (MII oocyte + PB1 + CB group), and then cultured without cytochalasin B. The average cleavage rate of reconstructed oocytes was 72.5% (48 of 66), and the blastocyst formation rate was 18.7% (9 of 48). Chromosome analysis showed similar proportions of haploid and diploid cells in the control (normal MII oocytes) and CR groups after PA; overall, 23.6% of blastocysts were tetraploid in the MII oocyte + PB1 + CB group. These results demonstrate that chromosomes in PB1 can participate in normal pre-implantation embryonic development when injected into enucleated MII stage oocytes, and that tetraploid PA blastocysts are produced (although at a low proportion) when PB1 chromosomes are injected into intact MII stage oocytes.

Highlights

  • The chromosomes in the first polar body (PB1) have the same genetic potential as their sister chromosomes remaining in the oocyte [1,2,3,4,5]

  • Oocytes with a uniform ooplasm and compact cumulus cell mass were selected for in vitro maturation. These Cumulus Oocyte Complexes (COCs) were cultured in 500 μl TCM medium supplemented with 10% porcine follicular fluid (PFF), 10 ng/ml epidermal growth factor (EGF), 10 IU/ml PMSG and 10 IU/ml hCG in each well of a four-well multi dish

  • The present study examined two type of reconstructed oocytes: 1) enucleated MII stage oocytes injected with PB1 chromosomes; and 2) intact MII stage oocytes injected with PB1 chromosomes (MII oocyte + PB1 group)

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Summary

Introduction

The chromosomes in the first polar body (PB1) have the same genetic potential as their sister chromosomes remaining in the oocyte [1,2,3,4,5]. Studies have shown that the polar bodies of mice are capable of participating in normal embryonic development in vitro and in vivo; producing normal offspring [2,3,4,5] or parthenogenetic embryonic stem (ES) cell lines [1]. It is difficult to extrapolate mouse results to large domestic animals because the latter require a much longer interval for oocyte development in vitro. Chimeras produced with tetraploid embryos and ES cells, can produce genetically modified animals and may offer an alternative to somatic cell nuclear transfer.

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