Yale Bulletin and Calendar

December 6-13, 1999Volume 28, Number 15



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Scientists' characterization of yeast gene
may yield clues about how human cells work

In the largest genome project of its kind to date, Yale scientists have succeeded in fully characterizing the function of the yeast gene, furthering understanding of how human cells work.

"While the human genome project so far has focused on the discovery of new genes, our study has taken gene discovery to the next level by figuring out how the genes work," says Michael Snyder, professor and chair of molecular, cellular and developmental biology. "We were pleasantly surprised to discover new genes in the process."

Because as many as 70 percent of yeast genes are strikingly similar to human genes, information about the yeast gene is expected to enhance understanding about human genes and may provide insight into human diseases, says Snyder, whose work is published in the Nov. 25 issue of Nature.

"When a human gene is discovered that has been implicated in a genetic disease such as cancer, knowing how the accompanying yeast gene works can help in designing appropriate treatments to help cure the disease," Snyder says. "The yeast gene is basically a small person. It is very easy to manipulate and is very similar to the cellular processes of human cells."

During the five-year study, Snyder's team invented a novel method of inserting pieces of DNA throughout the yeast genome. This method helps characterize the yeast gene by determining when the genes are active and also creates mutations in genes so that the functions of the genes can be analyzed. The Yale team analyzed 2,000 genes, or approximately one-third of the genes encoded in the yeast genome.

"We have discovered new genes and we can now help determine functions for many genes that had been discovered previously, but which had not been characterized," says Snyder, who is also a professor of biophysics and biochemistry. "It helps us understand both the genetic blueprint and what that blueprint actually does."

The study establishes both an information database and a set of tools that many researchers in the scientific community can use.

"Thousands of people have visited our database to help learn new things about the genes that they may either already be studying or interested in studying," says Snyder. "This helps give them clues to what experiments to try next.

"Having one thousand labs with the tools to analyze thousands of genes will provide the most detailed understanding of gene function imaginable," he adds. "By comparing the characteristics of thousands of genes, we can understand relationships that we did not realize existed before."

Snyder's team consisted of researchers from several Yale laboratories, including Shirleen Rodeur of the department of molecular, cellular and developmental biology; Perry Miller of the Center for Medical Informatics and the department of anesthesiology; and Mark Gerstein of the department of molecular biophysics and biochemistry.

-- By Karen Peart


T H I SW E E K ' SS T O R I E S

Divinity School gets $6 million grant

CMI will boost faculty's use of new media

'Accelerated life' suits Yale's youngest star

From the University Provost

Endowed Professorships

Gifts support use of new technologies in teaching and learning

Yale SOM experts take to the airwaves

Actors must connect with their characters, says Pacino

Interior Secretary to discuss environmental ethics

Ralph Reed to give lecture at Law School

Scientists' characterization of yeast gene may yield clues about how human cells work

Keith Wilson earns high honors for his musical contributions

Drama takes audience on metaphysical train ride

Doctor helps design Disney exhibit on high-tech world of radiology

Yale-related renovation projects win design awards

Researcher wins competitive McKnight Investigator Award

Duke's Men to perform in the 'Do Downtown' lunchtime series

Holiday Toys for Kids drive

Modest measures advised in preparation for Y2K

Hawkshaw speaks at conference on Bruckner

. . In the News . . .


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