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Research group Erich Nigg

News Details

07.07.2015

Two are better than one – another checkpoint enzyme for flawless cell division

The error-free distribution of genetic material during cell division is important for preventing the development of tumor cells. Prof. Erich Nigg’s research group at the Biozentrum, University of Basel, has uncovered a new important function of the human enzyme Plk1. It plays a significant role in monitoring chromosome segregation. The results published in the journal "Cell Reports" may provide important clues for the treatment of cancer.

Mitotic spindle apparatus preparing for chromosome segregation: an unaligned chromosome activates the checkpoint (green) and thereby prevents premature segregation.

Each day, the cells of the human body divide billions of times; this also requires duplication of their genetic information. Errors in cell division can cause tumor formation, and an exact segregation of the DNA (chromosomes) is therefore essential to ensure the health of the whole organism. Prof. Erich Nigg’s research group at the Biozentrum, University of Basel, has demonstrated that the enzyme Plk1 plays a significant role in monitoring the segregation of chromosomes.

Plk1 has checkpoint function

The segregation of the 23 chromosome pairs of human cells only occurs when all parameters are correct. This is ensured by a surveillance process, a so-called checkpoint. Central to this checkpoint is an inhibitor formed on the chromosomes, called mitotic checkpoint complex (MCC), which prevents cell division until all settings on the mitotic spindle, the chromosome segregation apparatus, are correct. “Just like the enzyme Mps1, Plk1 also ensures the assembly of the MCC and finally the inhibition of cell division,” says the first author Conrad von Schubert. “Plk1 thus also has a checkpoint function and consequently safeguards chromosome segregation.”

In the past, various functions have been attributed to the enzyme Plk1, including the correct assembly and disassembly of the mitotic spindle. “The newly uncovered checkpoint function of Plk1 had been overlooked, however, since other functions obscured this phenomenon,” explains Conrad von Schubert. The research team could now demonstrate that Plk1 influences the inhibitor MCC via at least two pathways. In a nutshell, Plk1 supports the enzyme Mps1, whose checkpoint function had already been known for some time. “Plk1 ensures rapid and robust checkpoint activation by acting in a similar way to Mps1, thus reinforcing Mps1 activity,” says Conrad von Schubert.

Plk1 demonstrates evolutionary stability

“While Plk1 and Mps1 cooperate in human cells, Plk1 has prevailed over Mps1 during the evolution of other organisms,” remarks Conrad von Schubert. Because Mps1 has disappeared in the nematode Caenorhabditis elegans, Plk1 has taken over the entire checkpoint function in this organism, as shown by an independent study in the same issue of the journal.

Combined drugs against cancer?

Mps1 is currently being investigated as a possible target for the treatment of cancer. “However, the fact that Plk1 also exhibits checkpoint function during cell division was not known,” says Conrad von Schubert. The new findings suggest that both enzymes should be considered as targets for cancer therapy. “Drugs against Plk1 were developed some time ago and, in light of our findings, it would be interesting to test the potential of a combinatorial treatment.”

Original article:
Conrad von Schubert, Fabien Cubizolles, Jasmine M. Bracher, Tale Sliedrecht, Geert J.P.L. Kops, and Erich A. Nigg (2015): Plk1 and Mps1 Cooperatively Regulate the Spindle Assembly Checkpoint in Human Cells. Cell Reports, published online June 25, 2015.

Contact: Communications, Heike Sacher