Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo.
Author(s) -
L. R. Fraser,
I. Maudlin
Publication year - 1979
Publication title -
environmental health perspectives
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.257
H-Index - 282
eISSN - 1552-9924
pISSN - 0091-6765
DOI - 10.1289/ehp.7931141
Subject(s) - biology , aneuploidy , embryo , spermatozoon , human fertilization , chromosome , in vivo , meiosis , chromosome segregation , premature chromosome condensation , genetics , ploidy , blastomere , cleavage (geology) , sperm , in vitro fertilisation , andrology , embryogenesis , gene , medicine , paleontology , fracture (geology)
First-cleavage mouse embryos, fertilized in vitro and in vivo, provide ideal material for chromosomal analysis. With the appropriate incubation in a mitotic inhibitor, syngamy is prevented and the sperm- and egg-derived chromosomes remain as separate clusters. Because the latter chromosomes undergo condensation sooner than those from the spermatozoon, the parental source of chromosome sets can be identified even without a marker chromosome. Thus these embryos can be analyzed both for the primary incidence and the parental source of a number of chromosomal anomalies, including aneuploidy. By using fertilization in vitro to obtain the embryos, the synchrony of fertilization and nuclear development is such that 80% or more of the chromosomal preparations are suitable for analysis, compared with about 50% for embryos fertilized in vivo.
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