Genome sequencing and comparative analysis of <i>Saccharomyces cerevisiae</i> strain YJM789

Wei Wu(Chinese Academy of Sciences), John H. McCusker(Duke Medical Center), Richard W. Hyman(Stanford University), Ted Jones(Stanford University), Ning Ye(European Molecular Biology Laboratory), Zhiwei Cao(Shanghai Center For Bioinformation Technology), Zhenglong Gu(Cornell University), Dan Bruno(Stanford University), Molly Miranda(Stanford University), Michelle Nguyen(Stanford University), Julie Wilhelmy(Stanford University), C. Komp(Stanford University), Raquel Tamse(Stanford University), Xiaojing Wang(Chinese Academy of Sciences), Peilin Jia(Chinese Academy of Sciences), Philippe P. Luedi(Duke Medical Center), Peter J. Oefner(Stanford University), Lior David(Stanford University), Fred S. Dietrich(Duke Medical Center), Yixue Li(Chinese Academy of Sciences), Ronald W. Davis(Stanford University), Lars M. Steinmetz(European Molecular Biology Laboratory)
Proceedings of the National Academy of Sciences
July 26, 2007
Cited by 254Open Access
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Abstract

We sequenced the genome of Saccharomyces cerevisiae strain YJM789, which was derived from a yeast isolated from the lung of an AIDS patient with pneumonia. The strain is used for studies of fungal infections and quantitative genetics because of its extensive phenotypic differences to the laboratory reference strain, including growth at high temperature and deadly virulence in mouse models. Here we show that the approximately 12-Mb genome of YJM789 contains approximately 60,000 SNPs and approximately 6,000 indels with respect to the reference S288c genome, leading to protein polymorphisms with a few known cases of phenotypic changes. Several ORFs are found to be unique to YJM789, some of which might have been acquired through horizontal transfer. Localized regions of high polymorphism density are scattered over the genome, in some cases spanning multiple ORFs and in others concentrated within single genes. The sequence of YJM789 contains clues to pathogenicity and spurs the development of more powerful approaches to dissecting the genetic basis of complex hereditary traits.


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