Uterine differentiation in cattle and sheep begins prenatally, but is compl
eted postnatally. Mechanisms regulating this process are not well defined.
However, studies of urogenital tract development in murine systems, particu
larly those involving tissue recombination and targeted gene mutation, indi
cate that the ideal uterine organizational programme evolves epigenetically
through dynamic cell-cell and cell-matrix interactions that define the mic
roenvironmental context within which gene expression occurs and may ensure
adult tissue stability. In the cow and ewe, transient postnatal exposure of
the developing uterus to steroids can produce immutable changes in adult u
terine tissues that may alter the embryotrophic potential of the uterine en
vironment. Thus, success of steroid-sensitive postnatal events supporting u
terine growth and development can dictate the functional potential of the a
dult uterus. Studies to determine effects of specific steroidal agents on p
atterns of uterine development during defined neonatal periods, as well. as
the functional consequences of targeted neonatal steroid exposure in the a
dult uterus, should enable identification of critical developmental mechani
sms and determinants of uterine integrity and function. Extreme adult uteri
ne phenotypes (lesion models) created in cattle and sheep by strategic post
natal steroid exposure hold promise as powerful tools for the study of fact
ors affecting uterine function and the rapid identification of novel uterin
e genes.