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A new method to analyse the genomes of yeast families

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Published on Monday, 13 May 2013

Researchers at the Institute for Systems Biology in Seattle (USA) and the Luxembourg Centre for Systems Biomedicine (LCSB) at the University of Luxembourg have jointly developed a revolutionary method to analyse the genomes of yeast families. The team of Dr. Aimée Dudley from the ISB and Dr. Patrick May from LCSB published their paper in the renowned scientific journal Nature Methods on May 12th. It describes a new method called BEST: Barcode Enabled Sequencing of Tetrads (DOI: 10.1038/nmeth.2479).

Baker’s yeast is one of the most powerful and widely used organisms in genetic research because of the ability to perform a technique called tetrad analysis. Matings between two yeast “parents” produce four yeast “children” or spores that stick together as “tetrads”. To genetically analyse these progeny, one needs to physically separate (“dissect”) the four spores of each tetrad.

The current method for doing this is extremely labour-intensive and has remained essentially unchanged for 75 years. A number of methods have tried to circumvent this manual process, but until now, none has been able to capture a crucial piece of information, the tetrad relationships between the spores.

The research team designed a new method that is several hundred times faster and is based on the following principles: First, two DNA sequences are added to the cells: A short sequence, called a barcode, that labels spores that come from the same tetrad and additionally a GFP (Green Fluorescent Protein) reporter gene. This fluorescent reporter allows the separation of tetrads away from other types of yeast cells by FACS sorting.

Then, the four spores of the tetrad are disrupted using a specific enzymatic reaction and allowed to grow up as individuals. Ultimately, the barcode and the same 2-3% of each individual’s genome are sequenced allowing the spore strain to be placed in the correct position of the family tree for further genetic analysis.

“Identifying the genes that underlie complex traits requires extremely large numbers of progeny and high volumes of DNA sequencing,” says Patrick May. “BEST combines the power of a gold standard genetic technique with ultra-high-throughput genome sequencing in a way that will enable the study of problems that were previously not possible.”

Ludlow, C.L., Scott, A.C., Cromie, G.A., Jeffery, E.W., Sirr, A., May, P., Lin J., Hays, M., Gilbert, T., Dudley, A.M. (2013) High-throughput Tetrad Analysis.Nature Methods, 2013


Consult this publication in ORBi lu , the University of Luxembourg's Open Access Repository: http://orbilu.uni.lu/handle/10993/1413



Photo caption:

BEST method: The plasmid library transformed into the yeast parents provides a unique barcode to each tetrad (4 yeast children) and permits the FACS (by GFP fluorescence) of tetrads away from other yeast cells. Tetrads are sorted onto an agar plate, where they are enzymatically digested and disrupted to allow each spore to form a colony. Colonies then are transferred into 96-well plates for genotyping and phenotyping. The plasmid barcode is read during genotyping and is used to identify the sister spores derived from each tetrad.