| |
Focus
Research in our laboratory focuses on mammalian germ cell development
with the aim of increasing our understanding of the genetic control
of sex determination and of the meiotic process in mammals. Our
research involves studies of both humans and mice.
We are conducting studies of human oocytes in association with
the Department of Reproductive Biology at University Hospitals.
The aim of this research is to elucidate the basis of the maternal
age effect in the human female; that is, to determine why, as women
age, they are at an increased risk of producing chromosomally abnormal
children. Although we know that the maternal age effect is the result
of meiotic errors in the egg and that most errors occur during the
completion of the first meiotic division (around the time of ovulation),
the mechanism by which age increases the frequency of errors remains
unknown. Recent studies in our laboratory suggest that, with increasing
age, the growth process of the human oocyte may become perturbed
(Volarcik et al., 1998). Hence one goal of our research is to understand
how changes in the environment in which the oocyte undergoes its
final growth and maturation effect the meiotic process.
In addition, we are studying a number of different mouse mutants
to understand the genetic control of the meiotic cell cycle in mammals
and the factors that influence meiotic chromosome alignment and
segregation. These studies make use of new techniques for the in
vitro growth of murine follicles, the production of chimeric ovaries,
the analysis of meiotic cell cycle progression and the analysis
of meiotic chromosome behavior. Our recent studies suggest that
the control of mammalian female meiosis differs in fundamental respects
from both male meiosis and mitosis and that these differences may
provide a key to understanding the high error rate in female meiosis
(LeMaire-Adkins et al., 1997).
|
|

|
|
|
|