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J. Biol. Chem., Vol. 269, Issue 50, 31383-31389, Dec, 1994
L Hiser, ME Basson and J Rine
Two recessive alleles of ERG10 and three temperature-sensitive recessive
alleles of HMG1 (3-hydroxy-3-methyl-glutaryl-CoA reductase isoenzyme 1)
were isolated in a screen for mevalonate auxotrophs in Saccharomyces
cerevisiae. The essential, single-copy ERG10 gene was cloned by
complementation of the temperature-sensitive phenotype of erg10-21. The
1,194-base pair continuous open reading frame, encoding a 398-amino acid
polypeptide with a calculated molecular mass of 41,681 daltons, was
demonstrated to encode cytoplasmic aceto-acetyl-CoA thiolase.
Acetoacetyl-CoA thiolase activity corresponded to the number of copies of
ERG10 present in cell extracts, and null alleles of ERG10 produced no
detectable acetoacetyl-CoA thiolase enzyme activity. The deduced amino acid
sequence was 40-95% identical to acetoacetyl-CoA thiolases from other
organisms. This identity included the active site cysteines located at
amino acids 91 and 384 in the Erg10 protein.
ERG10 from Saccharomyces cerevisiae encodes acetoacetyl-CoA thiolase
Department of Molecular and Cell Biology, University of California, Berkeley 94720.
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