Exposure of growing hyphae of Neurospora crassa to heat shock (44 degr
ees C) or ethanol (2.6 M) for 1 h induced a significant increase in th
e cAMP level, which reached a maximum approximately 2 min after the be
ginning of treatment and then decreased to control values despite cont
inued heat or ethanol exposure. A 10-s heat shock or a 5-s ethanol sho
ck also resulted in a transient cAMP increase 2 min after the pulse. H
eat shock or ethanol treatment led to an increase in the amount of cat
alytic subunits of the cAMP-dependent protein kinase A in the nucleus
almost synchronously with the increase of cAMP in the cytoplasm. The c
oncentration of cGMP decreased a few seconds after the beginning of he
at shock (44 degrees C) or ethanol treatment (2.6 M) to approximately
50% of the control level. Exposure to heat shock (44 degrees C, 1 h) l
ed to an increase in the amount of inositol phosphates 0.5-2 min after
the onset of heat shock. Thereafter, inositol phosphate levels droppe
d to control values despite continued heat exposure. Incubation of gro
wing hyphae with cAMP or 8-Br-cAMP led to a two- to threefold increase
of inositol phosphates 10-300 s after the beginning of incubation. He
at treatment furthermore caused a rapid release of calcium from vacuol
es as determined by Fura-2 measurement of the calcium content released
from isolated vacuoles. These heat-shock-dependent second messenger c
hanges may play a role in the heat-shock-induced phase shifts of the c
ircadian clock and heat-shock-induced conidiation.