In Saccharomyces cerevisiae, utilization of galactose requires four inducible enzyme activities. Three of these activities (galactose-l-phosphate uridyl transferase, EC 2.7.7.10; uridine diphosphogalactose 4-epimerase, EC 5.1.3.2; and galactokinase, EC 2.7.1.6) are specified by three tightly linked genes (GAL7, GALlO, and GALI, respectively) on chromosome II, whereas the fourth, galactose transport, is specified by a gene (GALS) located on chromosome XIL Although classic genetic analysis has revealed both positive and negative regulatory genes that coordinately affect the appearance of ail four enzyme activities, neither the basic events leading to the appearance of enzyme activities nor the roles of the regulatory genes have yet been determined. Regulation of inducible enzyme activity could be mediated by events related to transcription, tra n, or enzyme activation. For the purpose of studying galae thway induction and its regulation, we have developedan _unoprecipitation assay that enables us to detect the GAL7specifieduridyl transferase polypeptide in yeast extracts and among the polypeptides synthesized in an RNA-dependent in vitro translation system. Use of this immunoprecipitation assay in conjunction with in vivo labeling experiments demonstrates the presence of [3Hleucine-labeled transferase in extracts prepared from cells grown in galactose but not from cells grown in glucose. This gaactose-specific induction of transferase polypeptide is mediated by the de novo appearance of a functional mRNA species whose synthetic capacity is detectable by the combination of in vitro translation and immunoprecipitation. The appearance of functional th ge ST=RNA depends on wild-type expression of the _qlatory gene, GALA. Cells carrying a nonsense _ aion in the GALA gene fail to produce the trans___lA, whereas a nonsense suppressor of the GALA __utant regains the galactose-specific mRNA response.Results estab ish that the induction of the GAL7 specified uridyl transferase activity is mediated by de novo appearance of a functional mRNA and that this galactose-specific response is dependent a wild-type GALA gene product. In the simple eukaryote, Saccharomyces cerevtslae, the utilization of carbon from exogenously provided galactose requires