TY - JOUR
T1 - Structural requirements for activity of the pheromones of Ustilago hordei
AU - Kosted, Paula J.
AU - Gerhardt, Shirley A.
AU - Anderson, Cynthia M.
AU - Stierle, Andrea
AU - Sherwood, John E.
N1 - Funding Information:
This research was supported by USDA/NRICGP Grant 94-37303-0765 and the Montana Agricultural Experiment Station.
PY - 2000/3
Y1 - 2000/3
N2 - Ustilago hordei, the cause of barley-covered smut, initiates mating with pheromones. Gene sequence analysis suggested that these pheromones, Uhmfa1 and Uhmfa2, would be farnesylated peptides. Although isolation of mating-type-specific activity was rarely possible, chromatographic separations of culture supernatants yielded fractions that stimulated or inhibited mating. Based on predicted amino acid sequences and mass spectra of stimulating fractions, a series of pheromone analogs were synthesized and their activities were determined. Underivatized Uhmfa1 (PGKSGSGLGYSTC) or Uhmfa2 (EGKGEPAPYC) peptides were inactive, while peptides that were farnesylated and/or methyl esterified specifically induced conjugation tubes by cells of the opposite mating type. Uhmfa1 truncated from the amino terminus beyond the lysine lost activity, while truncated Uhmfa2 remained partially active. In mating bioassays, a pheromone concentration-dependent default mating response was observed. In competition studies, shorter Uhmfa1 peptides lacking pheromone activity inhibited activity of full-length peptides most effectively when both had the same functional groups. (C) 2000 Academic Press.
AB - Ustilago hordei, the cause of barley-covered smut, initiates mating with pheromones. Gene sequence analysis suggested that these pheromones, Uhmfa1 and Uhmfa2, would be farnesylated peptides. Although isolation of mating-type-specific activity was rarely possible, chromatographic separations of culture supernatants yielded fractions that stimulated or inhibited mating. Based on predicted amino acid sequences and mass spectra of stimulating fractions, a series of pheromone analogs were synthesized and their activities were determined. Underivatized Uhmfa1 (PGKSGSGLGYSTC) or Uhmfa2 (EGKGEPAPYC) peptides were inactive, while peptides that were farnesylated and/or methyl esterified specifically induced conjugation tubes by cells of the opposite mating type. Uhmfa1 truncated from the amino terminus beyond the lysine lost activity, while truncated Uhmfa2 remained partially active. In mating bioassays, a pheromone concentration-dependent default mating response was observed. In competition studies, shorter Uhmfa1 peptides lacking pheromone activity inhibited activity of full-length peptides most effectively when both had the same functional groups. (C) 2000 Academic Press.
KW - Cell growth arrest
KW - Conjugation tube
KW - Default mating
KW - Farnesyl group
KW - Lipopeptide pheromone
KW - Methyl ester
KW - Peptide
UR - http://www.scopus.com/inward/record.url?scp=0033937644&partnerID=8YFLogxK
U2 - 10.1006/fgbi.2000.1191
DO - 10.1006/fgbi.2000.1191
M3 - Article
C2 - 10919379
AN - SCOPUS:0033937644
SN - 1087-1845
VL - 29
SP - 107
EP - 117
JO - Fungal Genetics and Biology
JF - Fungal Genetics and Biology
IS - 2
ER -