Genome sequencing and comparative analysis of Saccharomyces cerevisiae strain YJM789

被引:211
作者
Wei, Wu
McCusker, John H.
Hyman, Richard W.
Jones, Ted
Ning, Ye
Cao, Zhiwei
Gu, Zhenglong
Bruno, Dan
Miranda, Molly
Nguyen, Michelle
Wilhelmy, Julie
Komp, Caridad
Tamse, Raquel
Wang, Xiaojing
Jia, Peilin
Luedi, Philippe
Oefner, Peter J.
David, Lior
Dietrich, Fred S.
Li, Yixue
Davis, Ronald W.
Steinmetz, Lars M. [1 ]
机构
[1] Chinese Acad Sci, Grad Sch, Shanghai Inst Biolsci, Key Lab Syst Biol,Bioinformat Ctr, Shanghai 200031, Peoples R China
[2] Shanghai Ctr Bioinformat Technol, Shanghai 200235, Peoples R China
[3] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[4] Stanford Univ, Dept Biochem, Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
[5] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
[6] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
comparative genomics; genome architecture; introgression; lateral gene transfer;
D O I
10.1073/pnas.0701291104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 approximate to 12-Mb genome of YJM789 contains approximate to 60,000 SNPs and approximate to 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.
引用
收藏
页码:12825 / 12830
页数:6
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