Ooplasmic donation in humans - The potential for epigenic modifications

被引:44
作者
Hawes, SM [1 ]
Sapienza, C
Latham, KE
机构
[1] Monash Univ, Inst Reprod & Dev, Ctr Early Human Dev, Melbourne, Vic 3168, Australia
[2] Temple Univ, Sch Med, Fels Inst Canc Res & Mol Biol, Philadelphia, PA 19140 USA
[3] Temple Univ, Sch Med, Dept Pathol, Philadelphia, PA 19140 USA
[4] Temple Univ, Sch Med, Dept Biochem, Philadelphia, PA 19140 USA
关键词
assisted reproduction; mitochondrial heteroplasmy; ooplasm donation;
D O I
10.1093/humrep/17.4.850
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Ooplasm donation, wherein ooplasm is transferred from a donor oocyte to a recipient oocyte in an effort to increase embryo viability, has been applied in the human, with resulting pregnancies and births. Neither the safety nor efficacy of this method has been adequately investigated. Mitochondrial heteroplasmy in the blood of children conceived using ooplasm donation has recently been described. A follow-up study of children born following the use of this technique primarily focused on the presence of mitochondria from the donor oocyte highlighting possible problems due to mitochondrial heteroplasmy. Other effects related to epigenetic events may also arise, but have not been addressed. Studies using inbred mouse strains reveal that genetically diverse ooplasms can impose diverse epigenetic modifications on parental genomes. Incompatibilities produced by combining maternal genome and ooplasm from different genotypes leads to defects in gene expression and development. Such defects can be heritable and observed in the next generation. Given the potential for epigenetic modifications to arise following ooplasm donation, the safety and efficacy of this method need to be evaluated in a suitable animal model.
引用
收藏
页码:850 / 852
页数:3
相关论文
共 22 条
[1]   THE LOCUS OM, RESPONSIBLE FOR THE DDK SYNDROME, MAPS CLOSE TO SIGJE ON MOUSE CHROMOSOME-11 [J].
BALDACCI, PA ;
RICHOUX, V ;
RENARD, JP ;
GUENET, JL ;
BABINET, C .
MAMMALIAN GENOME, 1992, 2 (02) :100-105
[2]   Mitochondria in human offspring derived from ooplasmic transplantation [J].
Barritt, JA ;
Brenner, CA ;
Malter, HE ;
Cohen, J .
HUMAN REPRODUCTION, 2001, 16 (03) :513-516
[3]  
BARRITT JA, 2001, RBM ONLINE, V3
[4]   Culture of preimplantation embryos: Facts and artifacts [J].
Bavister, BD .
HUMAN REPRODUCTION UPDATE, 1995, 1 (02) :91-148
[5]   Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone [J].
Bean, CJ ;
Hunt, PA ;
Millie, EA ;
Hassold, TJ .
HUMAN MOLECULAR GENETICS, 2001, 10 (09) :963-972
[6]   Birth of infant after transfer of anucleate donor oocyte cytoplasm into recipient eggs [J].
Cohen, J ;
Scott, R ;
Schimmel, T ;
Levron, J ;
Willadsen, S .
LANCET, 1997, 350 (9072) :186-187
[7]   Ooplasmic transfer in mature human oocytes [J].
Cohen, J ;
Scott, R ;
Alikani, M ;
Schimmel, T ;
Munne, S ;
Levron, J ;
Wu, L ;
Brenner, C ;
Warner, C ;
Willadsen, S .
MOLECULAR HUMAN REPRODUCTION, 1998, 4 (03) :269-280
[8]   Mitochondria: potential roles in embryogenesis and nucleocytoplasmic transfer [J].
Cummins, JM .
HUMAN REPRODUCTION UPDATE, 2001, 7 (02) :217-228
[9]  
de Villena FPM, 2000, GENETICS, V155, P283
[10]   Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal ''DDK syndrome'' genes are linked [J].
deVillena, FPM ;
Naumova, AK ;
Verner, AE ;
Jin, WH ;
Sapienza, C .
MAMMALIAN GENOME, 1997, 8 (09) :642-646