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September 29, 2021 02:02 am

Identical Twins Carry Genetic Modifications No One Else Has

sciencehabit shares a report from Science.org: Identical twins are living proof of how genetics shapes our looks and traits. Now, researchers have found they carry a molecular signature on their DNA that no one else has -- one that becomes fixed in their cells early in development and stays with them into adulthood. This signature doesn't seem to influence a twin's health, but it could offer insights into how identical twinning happens. "It is a starting point" for solving "what is really an enigma," says Jenny van Dongen, a twin genetics researcher at Free University (VU), Amsterdam. The signature could also be used to test whether a person had a "vanishing twin," an identical twin that died in the womb. An international team led by van Dongen and VU twin genetics researcher Dorret Boomsma looked for clues in what's known as the epigenome. Patterns of chemical tags called methyl groups glom onto genes, turning them on or off. (Such epigenetic changes are responsible for everything from enabling Peruvians to live at high altitudes to helping the placenta develop.) Using blood and cheek cell samples, the researchers scanned the epigenomes of more than 3000 identical twins, as well as a comparable number of fraternal twins and some twins' parents. They looked at 400,000 different places on each person's genome. About 800 locations had differences in methylation that set identical twins apart from everyone else, the team reports today in Nature Communications. "It's likely something established very early on that is propagated to subsequent cells," van Dongen says. Some of the methylated or unmethylated spots made sense, such as tags on genes involved in cell adhesion that might influence how easily a fertilized egg splits into two embryos. But changes in other locations, such as the ends of chromosomes, don't have an obvious explanation. These regions have been associated with aging, yet identical twins' life spans are similar to other people's. An epigenetic test might also be useful to determine whether a person once had an identical twin that vanished in the uterus, perhaps because it didn't have enough room or nutrients to grow. Sometimes a twin fetus appears in an ultrasound before vanishing, but other times it may be absorbed without leaving a trace. As many as 12% of pregnancies start out as multiples (including fraternal twins), according to some estimates, but only 2% of twin pairs survive. Using a separate data set, the epigenetic signature could predict whether someone was an identical twin in 70% to 80% of cases, van Dongen says. With data from a large enough group of people, the test would get even better, she says, and it could also help "predict the exact rate" of vanishing twins. That figure would be useful not only for researchers, but also "of broad interest" to twins themselves and to families who are mourning the loss of an identical twin, Boomsma says.

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