The TATA-binding protein (TBP)-related factor 1 (TRF1) is expressed in a ti
ssue-restricted fashion during Drosophila embryogenesis and may serve as a
promoter-specific recognition factor that can replace TBP in regulating tra
nscription. However, bona fide target promoters that would preferentially r
espond to TRF1 have remained elusive. Polytene chromosome staining, chromat
in immunoprecipitation, direct messenger RNA analysis, and transient cotran
sfection assays identified the Drosophila gene tudor as containing a TRF1-r
esponsive promoter. Reconstituted in vitro transcription reactions and deox
yribonuclease I footprinting assays confirmed the ability of TRF1 to bind p
referentially and direct transcription of the tudor gene from an alternate
promoter. Thug, metazoans appear to have evolved gene-selective and tissue-
specific components of the core transcription machinery to regulate gene ex
pression.