News Release

Yeast screen uncovers genes involved in chromosomal mutation

A team led by researchers at Osaka University performed genetic screening of fission yeast to identify the key players that underlie gross chromosomal rearrangement, a type of chromosomal mutation

Peer-Reviewed Publication

Osaka University

Srr1 and Skb1 promote gross chromosomal rearrangements in fission yeast.

image: rad51 and srr1 skb1 rad51 cells grown on EMM+UA non-selective plates were transferred onto 5-FOA+UA selective plates, on which only the cells containing gross chromosomal rearrangements can grow. The srr1 skb1 mutation reduced cell growth on the selective plate. view more 

Credit: Takuro Nakagawa

Osaka, Japan – When creating a computer program, errors in the code can introduce bugs to the software. Similarly, errors in our body’s genetic code, DNA, which is stored in structures known as chromosomes, can bring about mutations in the body. These mutations are the cause of many deadly diseases – including cancer. Now, researchers in Japan have shed new light on a particular type of genetic mutation: gross chromosomal rearrangement (GCR).

In a new study published in Communications Biology, a multi-institutional team led by researchers from Osaka University analyzed fission yeast to identify two key genes involved in the process of GCR.

The researchers were particularly interested in the centromere, a region important for chromosome separation during cell division. The centromere contains repeating DNA sequences, and GCR is known to occur at areas where DNA sequences repeat. Rad51 is a key enzyme involved in DNA recombination that exchanges genetic material. In contrast to what one can expect, however, Rad51 suppresses rather than promotes GCR at the centromere. It is enigmatic how GCRs occur using the centromere repeat.

“To find genes that are involved in the occurrence of GCR, we introduced mutations to yeast lacking Rad51, which exhibit increased levels of GCR,” says senior author Takuro Nakagawa. “We searched for cells that showed reduced levels of GCR and found that cells with mutations in the genes Srr1 and Skb1 had less GCR, suggesting that these genes play a role in the occurrence of GCR.”

The researchers then deleted the Srr1 and Skb1 genes in yeast lacking Rad51 and evaluated the occurrence of GCR. Cells lacking Srr1 and cells lacking Skb1 exhibited reduced rates of GCR; cells lacking both genes exhibited even lower rates of GCR.

“Our analysis revealed that Srr1 and Skb1 are involved in the formation of isochromosomes, a type of structural mutation in the chromosome,” says the lead author of the study Piyusha Mongia. “Loss of Srr1 or Skb1 led to a significant reduction in the number of isochromosomes that occurred.”

The research team’s findings represent an important step toward understanding the mechanisms underlying GCR at the centromere. Because GCRs are involved in several genetic disorders, including cancer, understanding the process of GCR formation may advance our ability to treat certain genetic diseases.


The article, “Fission yeast Srr1 and Skb1 promote isochromosome formation at the centromere,” will be published in Communications Biology at DOI:

About Osaka University

Osaka University was founded in 1931 as one of the seven imperial universities of Japan and is now one of Japan's leading comprehensive universities with a broad disciplinary spectrum. This strength is coupled with a singular drive for innovation that extends throughout the scientific process, from fundamental research to the creation of applied technology with positive economic impacts. Its commitment to innovation has been recognized in Japan and around the world, being named Japan's most innovative university in 2015 (Reuters 2015 Top 100) and one of the most innovative institutions in the world in 2017 (Innovative Universities and the Nature Index Innovation 2017). Now, Osaka University is leveraging its role as a Designated National University Corporation selected by the Ministry of Education, Culture, Sports, Science and Technology to contribute to innovation for human welfare, sustainable development of society, and social transformation.



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