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J Cell Biol. 2010 January 11; 188(1): 2.
PMCID: PMC2812856
In This Issue

Segregating out UbcH10's role in tumorigenesis

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A single chromosome lags behind the others in a dividing cell overexpressing UbcH10.

Aubiquitin-conjugating enzyme that regulates the cell cycle promotes chromosome missegregation and tumor formation, say van Ree et al.

The mitotic E2 enzyme UbcH10 partners with the anaphase-promoting complex/cyclosome (APC/C) to ubiquitinate cell cycle regulators, targeting them for proteasomal destruction, and ensuring progression through mitosis. UbcH10 is overexpressed in a variety of human cancers, but whether it causes tumors or is simply up-regulated due to the increased number of proliferating cancer cells is unknown.

van Ree et al. generated mice expressing high levels of UbcH10 and found that they formed tumors in a broad range of tissues. Many of these tumors displayed aneuploidy—abnormal numbers of chromosomes resulting from errors in cell division. Live microscopy showed that cells expressing high amounts of UbcH10 had problems segregating sister chromatids correctly, possibly because the cells contained extra numbers of centrosomes that might complicate formation of a normal mitotic spindle. UbcH10 overexpression also reduced levels of the mitotic regulator cyclinB—a substrate of the APC/C—though it remains to be seen if this contributes directly to centrosome amplification and aneuploidy.

The same research group recently demonstrated that chromosome segregation defects drive tumorigenesis by promoting the loss of tumor suppressor genes like p53. Senior author Jan van Deursen now wants to investigate whether UbcH10 synergizes with other factors to promote chromosome instability in human cancers.

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Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press