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Defect in peroxisomal multifunctional enzyme MFE1 affects cAMP relay in Dictyostelium
Author(s) -
Matsuoka Satomi,
Kuwayama Hidekazu,
Ikeno Daisuke,
Oyama Masakazu,
Maeda Mineko
Publication year - 2004
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1111/j.1440-169x.2004.00732.x
Subject(s) - dictyostelium , peroxisome , microbiology and biotechnology , relay , enzyme , chemistry , biology , biochemistry , physics , receptor , gene , power (physics) , quantum mechanics
We have previously reported that cells of Dictyostelium discoideum lacking the fatty acid oxidation enzyme MFE1 accumulate excess cyclopropane fatty acids from ingested bacteria. Cells in which mfeA – is disrupted fail to develop when grown in association with bacteria but form normal fruiting bodies when grown in axenic media. Bacterially grown mfeA – cells express the genes for the cyclic AMP (cAMP) receptor ( carA ) and adenylyl cyclase ( acaA ) but fail to respond to a cAMP pulse by synthesis of additional cAMP which normally relays the signal. Moreover, they do not accumulate the adhesion protein, gp80, which is encoded by the cAMP‐induced gene, csaA . As a consequence, they do not acquire developmentally regulated EDTA‐resistant cell–cell adhesion. When mutant cells are mixed with wild‐type cells and allowed to develop together, they co‐aggregate and differentiate into both spores and stalk cells. Thus, most of the developmental consequences of excess cyclopropane fatty acids appear to result from impaired cAMP relay.