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   <subfield code="a">Fujimura</subfield>
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   <subfield code="u">Laboratory for Molecular Biology, Pharma Research Laboratories, Hoechst Japan Ltd., 1-3-2 Minamidai, 350, Kawagoe, Japan</subfield>
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   <subfield code="a">Molecular cloning of the DAC2/FUS3 gene essential for pheromone-induced G1-arrest of the cell cycle in Saccharomyces cerevisiae</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Hiro-aki Fujimura]</subfield>
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   <subfield code="a">Summary: Mating pheromones, known as a and α-factors, arrest the division of cells of opposite mating types, α and a respectively, in Saccharomyces cerevisiae. I have cloned the DAC2 gene, which is required for both pheromone-induced division-arrest and cell-fusion during conjugation. The constructed dac2::LEU2 null mutation leads to defects in both pheromone-induced divisionarrest and cell-fusion during conjugation; it also suppresses the growth defect caused by the gpal mutation (a mutation in the α subunit of the S. cerevisiae G protein). These results indicate that DAC2 may be the same gene as FUS3, which was recently isolated by Elion et al. (1990) as a gene essential for cell-fusion during conjugation. The dac2::LEU2 null mutant also showed morphological alterations in response to mating pheromones. I show here that the DAC2 product plays an essential role in both the division-arrest signalling pathway of the yeast pheromone response and in cell-fusion during conjugation.</subfield>
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   <subfield code="a">Pheromone response pathway</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Signal transduction</subfield>
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   <subfield code="a">Cell cycle control</subfield>
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   <subfield code="a">Yeast DAC2/FUS3 gene</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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