In the early Caenorhabditis elegans embryo, maternally expressed PIE-1 prot
ein is required in germ-line blastomeres to inhibit somatic differentiation
, maintain an absence of mRNA transcription, and block phosphorylation of t
he RNA polymerase II large subunit (Pol II) carboxy-terminal domain (CTD).
We have determined that PIE-1 can function as a transcriptional repressor i
n cell culture assays. By fusing PIE-1 sequences to the yeast GAL4 DNA-bind
ing domain, we have identified a PIE-1 repression domain that appears to in
hibit the transcriptional machinery directly. A sequence element that is re
quired for this repressor activity is similar to the Pol II CTD heptapeptid
e repeat, suggesting that the PIE-I repression domain might target a protei
n complex that can bind the CTD. An alteration of this sequence element tha
t blocks repression also impairs the ability of a transgene to rescue a pie
-1 mutation, suggesting that this repressor activity may be important for P
IE-1 function in vivo.