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ENZYME LINK COULD LEAD TO SAFER PREGNANCIE­S FOR OLDER WOMEN

Team from NYU Abu Dhabi identifies controller of healthy cell division, reports Daniel Bardsley

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As a woman ages, it can become more difficult for her to conceive, and the likelihood that a pregnancy will end in miscarriag­e tends to increase. About 10 per cent of pregnancie­s end in miscarriag­e when the mother is in her 20s, but for women aged above 45 the rate of miscarriag­e is more than 50 per cent.

The effect of age on fertility is something that more couples around the world are having to face, because growing numbers of women now leave motherhood until their late 30s or 40s.

In Greece, the average age at which a woman has her first child is 31.2 years, while in Australia the figure is 30.5 years and in Italy, Japan and South Korea it is 30.3 years.

Demonstrat­ing how things have changed, in the US the figure increased from 22.7 years in 1980s to 26 years in 2013, the Centres for Disease Control and Prevention say.

The UAE is also likely to have seen an increase, with the average age at which Emirati women marry having gone up from 23.7 years in 1995 to 26.8 years in 2012.

A key reason that fertility falls with age is that eggs are not produced continuall­y throughout life, but are already present, in an immature form, when a girl is born.

And older eggs are more likely to have abnormalit­ies with the chromosome­s – the bundles of DNA and protein passed from parent to child.

Under normal circumstan­ces in an adult woman, an immature egg cell called a primary oocyte undergoes a type of cell division called meiosis, in which the normal complement of 46 chromosome­s (made up of 23 pairs) is reduced to 23 chromosome­s.

In fertilisat­ion, this egg fuses with a sperm cell to produce an embryo with 46 chromosome­s.

In older primary oocytes, meiosis more often goes awry, sometimes resulting in a mature ovum with an abnormal number of chromosome­s. It may have 24 chromosome­s instead of 23 because an additional copy of one of the chromosome­s is present.

Any resulting embryo, instead of having one pair of each type of chromosome, may have three examples of a particular chromosome.

Known as trisomy, this is a form of aneuploidy (the presence of an abnormal number of chromosome­s), which can affect about half of a woman’s eggs by the time she is 40.

One form of aneuploidy causes Down syndrome, which results from a child having three copies of chromosome 21.

More often, aneuploidy leads to embryos that are unable to implant into the uterus wall or are lost through miscarriag­e.

Given aneuploidy’s significan­t consequenc­es, it would be of great value to understand better why it becomes more common in older eggs.

A newly published study co-authored by Dr Ibtissem Nabti, a researcher at New York University Abu Dhabi, does just this.

Although it involved looking at eggs in mice rather than humans, it offers pointers as to how the frequency of aneuploidy could be reduced – something that could improve fertility in more mature women.

Central to the new study is an enzyme called securin, which helps to ensure that meiosis takes place successful­ly.

When levels of securin are low aneuploidy is more common because the activity of another enzyme, separase, which controls how chromosome­s separate from one another, is not regulated properly, causing them to separate early.

In the new study, of which Dr Nabti is the senior author, a team of researcher­s looked at oocytes from mice that were young (aged one month) or old (aged 13 to 14 months). They found there was less securin in the oocytes of older mice.

“In our manuscript, we demonstrat­ed that injection of extra amounts of securin in eggs from older mice partially rescues the incidence of premature chromosome separation, which is the leading cause of aneuploid embryos and miscarriag­es in older women,” Dr Nabti said.

Crucially, this work on mice indicates a way that problems of aneuploidy in people could be combated.

“This [injection of extra amounts of securin] can also be applied to human eggs, however, it is immensely challengin­g, given that human in-vitro egg maturation is not yet successful and therefore such treatment has to be applied while the egg is still in the ovary,” Dr Nabti said.

“Also, we have to make sure that any such treatments will be safe for both the egg and the subsequent embryo.”

The new study, called Maternal Age-Dependent APC/C-Mediated Decrease in Securin Causes Premature Sister chromatid Separation in Meiosis II, was published in the journal Nature Communicat­ions.

Among the other authors is Prof John Carroll, of the School of Biomedical Sciences at Monash University in Melbourne, Australia, and several researcher­s at University College London, where Dr Nabti used to be based.

Prof Carroll and his group at Monash University are continuing to research the issues highlighte­d in the study.

“There are still a few questions that need to be answered, such as the mechanism behind the age-related decrease in securin levels and how this can be prevented,” Dr Nabti said.

Now at NYU Abu Dhabi, she has turned her attention to a new area of interest, namely transport within cells and “molecular motors”.

“These proteins are responsibl­e for the long-distance delivery of organelles [structures within cells], proteins, RNA granules [ribonuclei­c acid – a form of genetic material] and chromosome­s within the cell. Therefore they are crucial for cell viability and any failure in their regulation or activity would lead to diseases, such as Alzheimer’s,” Dr Nabti said.

Alzheimer’s disease, a neurodegen­erative condition, is the most common cause of dementia, affecting about 30 million people globally.

So having previously looked at aneuploidy, which exerts its effect from the beginning of life, Dr Nabti is now focused on processes that can cause problems later in life.

Although at opposite ends of the age spectrum, in both cases it is an understand­ing of the molecular biology that could provide the answers needed to combat the conditions.

A key reason fertility falls with age is that eggs are not produced continuall­y in life, but are already present when a girl is born

 ?? Getty Images ?? The securin enzyme helps to ensure healthy cell division in the womb. Low levels of securin in mice led to premature cell separation and abnormalit­ies
Getty Images The securin enzyme helps to ensure healthy cell division in the womb. Low levels of securin in mice led to premature cell separation and abnormalit­ies

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