Northern analysis showed that accumulation of Agaricus bisporus cel1 m
RNA was regulated by two independent mechanisms: (i) induction by cell
ulose; and (ii) repression by glucose and other sugars. Isolated A. bi
sporus nuclei were transcriptionally active. Nuclei isolated from cell
ulose-grown mycelium synthesized six times more cel1 mRNA than nuclei
from glucose-grown mycelium. The start point of transcription (tsp) wa
s identified by primer extension and S1 nuclease analysis. Putative gl
ucose-, and cAMP-responsive elements as well as regions with homology
to promoter regions of other fungal cellulase genes were detected both
upstream and downstream from the tsp of the cel1 gene.