Signal transducers and activators of transcription (STATs) were discovered
as mediators of type I interferon-induced gene expression. This family of t
ranscription factors has been found in widespread signaling pathways, espec
ially those involving cytokines-regulating the immune response. Because a p
lethora and often confusing set of activators for STAT proteins was observe
d in cell culture models, it became important to define the physiologically
relevant actions of these molecules. One approach to this question has bee
n through the targeted disruption of STAT genes in transgenic mice. Now tha
t all seven STAT genes have been disrupted, both the high degree of STAT se
lectivity as well as many surprising and unexpected complexities are beginn
ing to be characterized.