When Dictyostelium cells starve, they begin secreting a glycoprotein called
conditioned medium factor (CMF). When there is a high density of starved c
ells, as indicated by a high concentration of CMF, the cells begin expressi
ng some genes and aggregate using pulses of cAMP as a chemoattractant. CMF
regulates gene expression via a G protein-independent pathway, whereas CMF
regulates cAMP signal transduction via a G protein-dependent pathway. To el
ucidate receptors mediating cell density sensing, we used CMF-Sepharose to
isolate membrane proteins that bind CMF. We identified a 50-kDa protein, CM
FR1, that is sensitive to trypsin treatment of whole cells. We obtained par
tial amino acid sequence of CMFR1 and isolated the cDNA encoding it, The de
rived amino acid sequence has no significant similarity to known proteins a
nd has two or three predicted transmembrane domains. Expression of CMFR1 in
insect cells caused an increase in CMF binding. Repression of CMFR1 in Dic
tyostelium by gene disruption resulted in a similar to 50% decrease of the
CMF binding and a loss of CMF-induced G protein-independent gene expression
. The G protein-dependent CMF signal transduction pathways appear to be fun
ctional in cmfr1 cells, suggesting that cells sense the density-sensing fac
tor CMF using two or more different receptors.