The mammalian ME1 gene encodes a non-tissue-specific, helix-loop-helix
transcription factor that is enriched in morphogenetically active reg
ions during development, Regulation of mouse ME1 gene expression is co
ntrolled by a novel initiator (ME1 Inr) that promotes transcription fr
om the center of a 13 bp poly(dA) tract. We show here that the ME1 Inr
autonomously directs initiation from the poly(dA) tract both in vitro
and in vivo. This transcription was dependent upon two protein comple
xes; MBP alpha, which associated directly with the poly(dA) tract, and
MBP beta, which introduced an similar to 60 degrees bend immediately
downstream of the poly(dA) tract. The MBP alpha and MBP beta binding s
ites were strikingly conserved in homologous DNA from several mammalia
n species and the frog Xenopus laevis. These results suggest that the
ME1 Inr constitutes a robust nucleation site that promotes transcripti
on initiation in the absence of conventional promoter elements.