Considerable progress has been made in the selection and characterizat
ion of mutants that are defective in the synthesis of ergosterol in th
e yeast, Saccharomyces cerevisiae. Mutations in nearly every step of t
he yeast sterol biosynthetic pathway have been induced and selected. T
hese mutants have been used to elucidate the sequential order of steps
in sterol synthesis, to study the mode of action of antifungal agents
and to determine the method of resistance of some pathogenic fungi, a
nd to answer questions on the role of sterols in general cell biology.
Physiological examination of ergosterol null mutants, lacking all bio
chemical activity attributed to the particular gene, supports a role f
or ergosterol in a number of critical functions in the organism. Among
the physiological functions attributed to ergosterol are sparking and
bulking requirements, involvement in amino acid and pyrimidine transp
ort, resistance to antifungal agents and certain cations, and a requir
ement for respiratory activity. Those genetic null alleles discussed i
n this review are erg24, lacking the ability to reduce the Delta(14) d
ouble bond; erg6, unable to methylate C-24; and erg3, defective in the
C-5 desaturase. The different biochemical activities that are disrupt
ed in the ergosterol mutants support a role for ergosterol in a number
of critical functions in yeast.