During culmination of Dictyostelium aggregates, prespore and prestalk cells
undergo terminal differentiation to form spores and a cellular stalk. Disr
uption of the cell-fate gene stkA leads to a phenotype in which all the cel
ls destined to become spores end up as stalk cells. 'Stalky' mutants expres
s normal levels of prespore cell transcripts but fail to produce the culmin
ation-stage spore transcript spiA. The stkA gene encodes a putative GATA-ty
pe transcription factor (STKA). III order to identify possible downstream t
argets of STKA we used the technique of mRNA differential display and isola
ted four cDNA fragments that hybridise to mRNAs present during the later st
ages of development. All four gene tags were cloned and sequenced. mRNAs re
presented by these four sequence tags do not accumulate during culmination
of 'stalky' cells and therefore must be specific to the spore pathway. By s
creening a cDNA library, longer cDNAs for all four mere cloned and sequence
d. Three of these contained complete protein-coding regions while only a pa
rtial cDNA was recovered for the fourth. One of the corresponding proteins
has significant homology to a surface zinc metalloproteinase (GP63) of the
protozoan parasite Leishmania, while another is closely related to a human
pre-RNA binding protein (hnRNP R).