DNA discovery could help identify mothers at risk of pre-eclampsia

The human genome is riddled with relics of viral infections—bits of DNA from viruses that have been inserted in human DNA over millions of years and never left. Most are silent but some have taken on functional roles, particularly in organs that evolve relatively rapidly, including the placenta.

An international collaboration between geneticists, evolutionary biologists, bioinformaticians and clinicians has identified how some of these ancient viral DNA fragments are influencing new life today—specifically, helping regulate genes that control normal placenta development and operation. One particular gene, EPS8L1, when overexpressed, induces key features of pre-eclampsia, a potentially life-threatening disorder during pregnancy. The research was reported this week in Genome Biology.

“These findings connect a deep evolutionary process to a very modern clinical problem and point to a potential biomarker to detect pre-eclampsia risk before symptoms develop,” says Professor Zsuzsanna Izsvák, Group Leader of the Mobile DNA Lab at the Max Delbrück Center in Berlin and co-corresponding author.

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