Deciphering the Origin, Evolution, and Physiological Function of the Subtelomeric Aryl-Alcohol Dehydrogenase Gene Family in the Yeast Saccharomyces cerevisiae

• Published in: Applied and environmental microbiology Vol. 84; no. 1; pp. e01553 - 17
• Main Authors: Yang, Dong-Dong, de Billerbeck, Gustavo M., Zhang, Jin-jing, Rosenzweig, Frank, Francois, Jean-Marie
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.01.2018
• Subjects: Alcohol dehydrogenase; Alcohol Oxidoreductases - genetics; Alcohol Oxidoreductases - metabolism; Alcohols; Aldehydes; Aliphatic compounds; Aromatic compounds; Aryl-alcohol dehydrogenase; Baking; Baking yeast; Biodegradation; Brewing; Chromosomes; Cinnamaldehyde; Degradation; Dehydrogenase; Domestication; Evolution; Evolution, Molecular; Evolutionary and Genomic Microbiology; Food engineering; Fungal Proteins - genetics; Fungal Proteins - metabolism; Fungi; Gene expression; Genes; Genomes; Homology; Industrial applications; Life Sciences; Lignin; Lignocellulose; Missense mutation; Multigene Family - genetics; NADP; Nucleotide sequence; Oxidation; Phylogenetics; Phylogeny; Physiology; Pseudogenes - genetics; Repair; Saccharomyces cerevisiae; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae - metabolism; Substrates; Vanillin; Veratraldehyde; Yeast; AKR superfamily; pseudogenization; lignin; subtelomeric; evolution; aryl-alcohol dehydrogenases; Lignin; analyse phylogénique; Aryl-alcohol dehydrogenases; brewer s; yeast; Subtelomeric; saccharomyces cerevisiae; expression génique; Evolution; Pseudogenization; séquence génomique; gene expression; pseudogénisation
• ISSN: 0099-2240; 1098-5336; 1098-5336
• DOI: 10.1128/AEM.01553-17

Homology searches indicate that Saccharomyces cerevisiae strain BY4741 contains seven redundant genes that encode putative aryl-alcohol dehydrogenases (AAD). Yeast AAD genes are located in subtelomeric regions of different chromosomes, and their functional role(s) remain enigmatic. Here, we show that two of these genes, AAD4 and AAD14 , encode functional enzymes that reduce aliphatic and aryl-aldehydes concomitant with the oxidation of cofactor NADPH, and that Aad4p and Aad14p exhibit different substrate preference patterns. Other yeast AAD genes are undergoing pseudogenization. The 5′ sequence of AAD15 has been deleted from the genome. Repair of an AAD3 missense mutation at the catalytically essential Tyr 73 residue did not result in a functional enzyme. However, ancestral-state reconstruction by fusing Aad6 with Aad16 and by N-terminal repair of Aad10 restores NADPH-dependent aryl-alcohol dehydrogenase activities. Phylogenetic analysis indicates that AAD genes are narrowly distributed in wood-saprophyte fungi and in yeast that occupy lignocellulosic niches. Because yeast AAD genes exhibit activity on veratraldehyde, cinnamaldehyde, and vanillin, they could serve to detoxify aryl-aldehydes released during lignin degradation. However, none of these compounds induce yeast AAD gene expression, and Aad activities do not relieve aryl-aldehyde growth inhibition. Our data suggest an ancestral role for AAD genes in lignin degradation that is degenerating as a result of yeast's domestication and use in brewing, baking, and other industrial applications. IMPORTANCE Functional characterization of hypothetical genes remains one of the chief tasks of the postgenomic era. Although the first Saccharomyces cerevisiae genome sequence was published over 20 years ago, 22% of its estimated 6,603 open reading frames (ORFs) remain unverified. One outstanding example of this category of genes is the enigmatic seven-member AAD family. Here, we demonstrate that proteins encoded by two members of this family exhibit aliphatic and aryl-aldehyde reductase activity, and further that such activity can be recovered from pseudogenized AAD genes via ancestral-state reconstruction. The phylogeny of yeast AAD genes suggests that these proteins may have played an important ancestral role in detoxifying aromatic aldehydes in ligninolytic fungi. However, in yeast adapted to niches rich in sugars, AAD genes become subject to mutational erosion. Our findings shed new light on the selective pressures and molecular mechanisms by which genes undergo pseudogenization.