Clue found to why egg flaws seen in older women

The release of a human egg The protein is a key factor in the ovulation process

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Scientists say they are closer to knowing why older women are more likely to produce abnormal eggs.

The Newcastle University team saw a fall in levels of proteins called cohesins, essential for chromosomes to divide properly for fertilisation.

Writing in Current Biology, they said understanding this process could help develop ways to prevent cohesin loss.

Abnormal eggs are linked to infertility, miscarriage and conditions including Down's Syndrome.

Start Quote

This is a neat explanation”

End Quote Professor Adam Balen, British Fertility Society

It was already known that pregnancy problems in older women can be linked to eggs containing the wrong number of chromosomes, but not why this occurred.

Messy division

All the cells in the body, except for sperm and eggs, contain two copies of each chromosome.

Sperm and eggs must lose one copy in readiness for fertilisation, a complex process. Cohesins bind chromosomes together by entrapping them in a ring. This is essential for them to divide properly.

If there is too little cohesin, the structure can be too "floppy" for division to happen equally.

In eggs, the problem is compounded by the fact that the physical attachments which hold chromosomes together are established before birth and must be maintained by cohesins until the egg divides just before ovulation - which can be decades later.

The researchers looked at eggs from young and old mice - and found cohesin levels declined with age.

By tracking chromosomes during division in the egg, the Newcastle team found that the reduced cohesin in eggs from older females resulted in some chromosomes becoming trapped and unable to divide properly.

Lead researcher Dr Mary Herbert, of the Centre for Life at Newcastle University, said: "Reproductive fitness in women declines dramatically from the mid-thirties onwards. Our findings point to cohesin being a major culprit in this.

"The aged mice we used are equivalent to a woman in her early forties.

"Cohesin levels were very much reduced in eggs from older mice and the chromosomes underwent a very messy division resulting in the wrong number of chromosomes being retained in the egg."


She said the next step was to look at human egg development, and work out why cohesin is lost with age.

"If we can understand this, we will be in a better position to know if there is any possibility of developing interventions to help reduce cohesin loss."

But Dr Herbert added: "Undoubtedly, the best way for women to avoid this problem is to have their children earlier."

Adam Balen, professor of reproductive medicine and surgery at the Leeds Centre for Reproductive Medicine, said the study was scientifically very interesting.

"This is a neat explanation as to why we see mismatches in chromosomes as women get older."

But Professor Balen, who is also chair of the British Fertility Society's practice and policy committee, added it was "far too early to say" if the finding would have any bearing on clinical care for older women with fertility problems.

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