@article{mbs:/content/journal/micro/10.1099/00221287-144-9-2417, author = "Warit, Saradee and Walmsley, Richard M. and Stateva, Lubomira I.", title = "Cloning and sequencing of the Candida albicans homologue of SRB1/PSA1/VIG9, the essential gene encoding GDP-mannose pyrophosphorylase in Saccharomyces cerevisiae", journal= "Microbiology", year = "1998", volume = "144", number = "9", pages = "2417-2426", doi = "https://doi.org/10.1099/00221287-144-9-2417", url = "https://www.microbiologyresearch.org/content/journal/micro/10.1099/00221287-144-9-2417", publisher = "Microbiology Society", issn = "1465-2080", type = "Journal Article", keywords = "GDP-mannose", keywords = "Candida albicans", keywords = "glycosylation", keywords = "SRB1/PSA1/VIG9", keywords = "cell wall", abstract = "Two genomic fragments have been isolated from Candida albicans which strongly hybridize to SRB1/PSA1/VIG9, an essential gene which encodes GDP-mannose pyrophosphorylase in Saccharomyces cerevisiae. A common 2.5 kb Xbal-Pstl fragment has been identified, which Southern analysis suggests is most likely unique in the C. albicans genome. The fragment contains an ORF, which is 82% identical and 90% homologous to the Srb1p/Psa1p/Vig9p from S. cerevisiae, contains one additional amino acid at position 254 and is able to functionally complement the major phenotypic characteristics of S. cerevisiae srb1 null and conditional mutations. The authors therefore conclude that they have cloned and sequenced from C. albicans the bona fide homologue of SRB1/PSA1/VIG9, named hereafter CaSRB1. Northern analysis data indicate that the gene is expressed in C. albicans under conditions of growth in the yeast and hyphal form and suggest that its expression might be regulated.", }