The R4GI gene of Kluyveromyces lactis encodes a low-affinity glucose/fructose transporter. Its transcription is induced by glucose, fructose, and several other sugars. The RAG4, RAGS, and RAG8 genes are trans-acting genes controlling the expression of the RAG) gene. We report here the characterization of one of these genes, RAG5. The nucleotide sequence of the cloned RAGS gene indicated that it encodes a protein that is homologous to hexokinases of Saccharomyces cerevisiae. ragS mutants showed no detectable hexokinase or glucokinase activity, suggesting that the sugar kinase activity encoded by this gene is the only hexokinase in K. lactis. Both high-and low-affinity transport systems of glucose were affected in ragS mutants. The defect of the low-affinity component was found to be due to a block of transcription of the RAG) gene by the hexokinase mutation. In vivo complementation of the rag5 mutation by the K2 gene of S. cerevisiae and complementation of hxikl hxk2 mutations of S. cerevisiae by the RAGS gene showed that RAGS and HXK2 were equivalent for sugar-phosphorylating activity but that RA4GS could not restore glucose repression in the S. cerevisiae hexokinase mutants.

The RAG1 gene of Kluyveromyces lactis encodes a low-affinity glucose/fructose transporter. Its transcription is induced by glucose, fructose, and several other sugars. The RAG4, RAG5, and RAG8 genes are trans-acting genes controlling the expression of the RAG1 gene. We report here the characterization of one of these genes, RAG5. The nucleotide sequence of the cloned RAG5 gene indicated that it encodes a protein that is homologous to hexokinases of Saccharomyces cerevisiae. rag5 mutants showed no detectable hexokinase or glucokinase activity, suggesting that the sugar kinase activity encoded by this gene is the only hexokinase in K. lactis. Both high- and low-affinity transport systems of glucose were affected in rag5 mutants. The defect of the low-affinity component was found to be due to a block of transcription of the RAG1 gene by the hexokinase mutation. In vivo complementation of the rag5 mutation by the HXK2 gene of S. cerevisiae and complementation of hxk1 hxk2 mutations of S. cerevisiae by the RAG5 gene showed that RAG5 and HXK2 were equivalent for sugar-phosphorylating activity but that RAG5 could not restore glucose repression in the S. cerevisiae hexokinase mutants.