Pax genes encode transcription factors known to play crucial roles dur
ing the development of specific embryonic tissues. In humans and mice,
several abnormalities have been linked to deficiencies in Pax gene do
sage, indicating that normal development is particularly sensitive to
the level of Pax gene expression. Despite these facts, relatively litt
le is known about how these proteins act as transcriptional regulators
, In this study we define the transactivation domains of murine Pax-2,
an essential factor in kidney organogenesis. Within the COOH terminus
of Pax-2, amino acids 279-373 are essential for transactivation. Howe
ver, this region alone is insufficient for full transactivation when f
used to the paired domain alone or to a heterologous DNA binding domai
n. Mutation or deletion of the conserved octapeptide sequence results
in increased transactivation by Pax proteins. The octapeptide-mediated
repression is also seen within a heterologous context using the GAL4
DNA binding domain. Thus transactivation by Pax-2 relies upon several
regions within the COOH terminus and is down-modulated by the octapept
ide element.