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cDNA clones representing eight specific mRNAs abundantly expressed in a dikaryon of Schizophyllum commune but not in the progenitor monokaryons, were used to localize these mRNAs in whole colonies by in situ hybridization. A genomic clone for 18s rRNA was used to probe for rRNA. The colonies were grown on hybridization membranes, fixed, and treated with RNAase-depleted wall-lytic enzymes from Trichoderma harzianum to facilitate permeation -of the probes. RNAs in sectors of the colonies were then localized with (32P)DNA probes. Hybridization at different developmental stages showed that the specific mRNAs were only formed in parts of the colony where fruit-body initials arose. At later stages these mRNAs disappeared from abortive fruit bodies but remained high in fruit bodies continuing development.

In situ Localization of Specific RNAs in Whole Fruiting Colonies of Schizophyllum commune