The HNF3/fork head family includes a large number of transcription factors
that share a structurally related DNA binding domain. Bork head factors hav
e been shown to play important roles both during development and in the adu
lt. We now describe the cloning of a novel mammalian fork head factor that
we have named FHX ((f) under bar ork head (h) under bar omologous (X) under
bar (FHX), which is expressed in many adult tissues. In the embryo, FHX ex
pression showed a very early onset during the cleavage stages of preimplant
ation development. Polymerase chain reaction-assisted site selection experi
ments showed that FHX bound DNA with a dual sequence specificity. Sites rec
ognized by FHX could be classified into two different types according to th
eir sequences. Binding of FHX to sequences of each type appeared to occur i
ndependently, Our data suggest that either different regions of the fork he
ad domain or different molecular forms of this domain could be involved in
binding of FHX to each type of site. In transfection assays, FHX was capabl
e of activating transcription from promoters containing FHX sites of either
type.