The likelihood of a chromosomally abnormal conception increases strikingly with age, and is a contributory factor in the age- related decrease in fertility in women. The consequences of these errors to human health are profound. The most common type of abnormality, aneuploidy, is the leading cause of mental retardation and pregnancy failure in our species. The basis of the age effect remains unknown, but recent molecular studies indicate that meiosis I (MI, the time at which homologous chromosomes segregate) is a critical time point in the genesis of most meiotic errors. In this proposal we outline direct studies of human oocytes to examine the mechanism of non-disjunction and the age association for individual human chromosomes. In addition, we propose experimental studies using mouse oocytes to examine the factors that influence the mammalian female meiotic process. These experimental studies make use of mouse mutants and recently developed culture systems for the in vitro growth of murine oocytes as model systems for the study of age-related changes in the human meiotic process. Finally, the possibility that the early cleavage divisions of the mammalian embryo are prone to non-disjunction errors is addressed using a murine mutation with a high level of mitotic non-disjunction. The combined data from the proposed studies will provide information on the mechanism(s) responsible for the human maternal age effect. Ultimately this knowledge may be useful in refining the current procedures for human assisted reproduction and/or in designing programs for clinical intervention to provide women over the age of 35 with increased likelihood of achieving a normal pregnancy.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD031866-07
Application #
6363395
Study Section
Reproductive Biology Study Section (REB)
Program Officer
Tasca, Richard J
Project Start
1994-05-01
Project End
2005-02-28
Budget Start
2001-03-01
Budget End
2002-02-28
Support Year
7
Fiscal Year
2001
Total Cost
$307,311
Indirect Cost
Name
Case Western Reserve University
Department
Genetics
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Hunt, Patricia A; Jackson, Jodi M; Horan, Sonia et al. (2008) The mouse A/HeJ Y chromosome: another good Y gone bad. Chromosome Res 16:623-36
Hall, Heather; Hunt, Patricia; Hassold, Terry (2006) Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors. Curr Opin Genet Dev 16:323-9
Koehler, Kara E; Voigt, Robert C; Thomas, Sally et al. (2003) When disaster strikes: rethinking caging materials. Lab Anim (NY) 32:24-7
Hodges, C A; Ilagan, A; Jennings, D et al. (2002) Experimental evidence that changes in oocyte growth influence meiotic chromosome segregation. Hum Reprod 17:1171-80
Hodges, Craig A; Hunt, Patricia A (2002) Simultaneous analysis of chromosomes and chromosome-associated proteins in mammalian oocytes and embryos. Chromosoma 111:165-9
Hunt, Patricia A; Hassold, Terry J (2002) Sex matters in meiosis. Science 296:2181-3
Bean, Christopher J; Hassold, Terry J; Judis, LuAnn et al. (2002) Fertilization in vitro increases non-disjunction during early cleavage divisions in a mouse model system. Hum Reprod 17:2362-7
Bean, C J; Hunt, P A; Millie, E A et al. (2001) Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone. Hum Mol Genet 10:963-72
Hodges, C A; LeMaire-Adkins, R; Hunt, P A (2001) Coordinating the segregation of sister chromatids during the first meiotic division: evidence for sexual dimorphism. J Cell Sci 114:2417-26
Hassold, T; Sherman, S; Hunt, P (2000) Counting cross-overs: characterizing meiotic recombination in mammals. Hum Mol Genet 9:2409-19

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