In Specific Aim 1, we will
clone & sequence genes that are
differentially expressed between incipient testis and ovary in
snapping turtle and mouse embryos. We will then confirm sexually
dimorphic expression of these genes. Finally, we will compare cDNA
sequences to identify novel genes that are conserved in sequence
between these species and query electronic databases to identify
homologous genes in humans.
In Specific Aim 2, we will use fluorescence in situ hybridization
to determine which gonadal cell types express the conserved sex-determining
genes (Sertoli, Leydig, Granulosa, or Thecal cells, as well as
primordial germ cells).
These studies pioneer the fusion of comparative genomics and functional
genomics to identify coexpressed gene orthologs in a massively
parallel manner. Using this approach, we expect to identify novel
genes that are conserved in sequence, sexually dimorphic expression,
and cell-type specific expression in vertebrates with distinct
modes of sex determination. Such genes are highly likely to have
the same function in sex determination in all vertebrates, including
humans. This approach promises to speed the rate of discovery of
sex-determining genes in humans, which to date has been slow and
haphazard.