New understanding of why chromosome errors are high in women's eggs

March 18th, 2014 in Biology / Cell & Microbiology
Professor Keith Jones (standing) and Dr. Simon Lane. Credit: University of Southampton


Professor Keith Jones (standing) and Dr. Simon Lane. Credit: University of Southampton

A new study from the University of Southampton has provided scientists with a better understanding of why chromosome errors are high in women's eggs.

It is estimated that up to 60 per cent of eggs are affected by errors in how their divide, making it the leading cause of infertility. Chromosome errors also lead to conditions such as Down Syndrome and early pregnancy loss.

By using state-of-the-art imaging techniques, the Southampton researchers examined the most important process present in all cells to prevent chromosome errors – the Spindle Assembly Checkpoint (SAC) – and looked at how it behaves in oocytes (developing female sex cells). The SAC acts as a gatekeeper, only allowing a cell to pass through (and so divide) if its chromosomes are all ready to do so, in order to preserve the cell's identity and proper function. If cells don't have a SAC, or the SAC is damaged in some way when cells divide, often the inherit the wrong number of chromosomes.

The researchers, Dr Simon Lane and Professor Keith Jones from the University's Centre for Biological Sciences, found differences in the way SAC operates in eggs to all other . Dr Lane says: "We found that in oocytes, the classical model of how this gatekeeper works, from a closed gate to open gate, doesn't operate: instead the gate is continually left ajar. As such, an oocyte can divide its chromosomes and becomes aneuploid – a cell with fewer or more chromosomes than usual – quite easily, because the SAC isn't preventing the division."

Professor Keith Jones, who is Head of the Centre for Biological Sciences, says: "Our findings won't provide an immediate cure for preventing errors, but it gives us a better understanding for what is controlling chromosome division in eggs. Armed with such knowledge, we could potentially find ways of improving this control mechanism or alternatively find ways of screening eggs as they are dividing to detect a good egg from a bad egg – although this screening would obviously only benefit people in an IVF setting where are recovered from the patient."

More information: The paper 'Non-canonical function of SAC proteins after APC activation reduces aneuploidy in mouse oocytes' is published in the journal Nature Communications.

Provided by University of Southampton

"New understanding of why chromosome errors are high in women's eggs." March 18th, 2014. http://phys.org/news/2014-03-chromosome-errors-high-women-eggs.html