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Identical twins may not be so identical after all. Even though identical
twins supposedly share all of their DNA, they acquire hundreds of genetic changes
early in development that could set them on different paths, according to new
research. The findings, presented Friday (Nov. 9) here at the American Society
of Human Genetics meeting, may partly explain why one twin gets cancer while
another stays healthy. The study also suggests that these genetic changes are
surprisingly common. "It's not as rare as people previously
expected," said study presenter Rui Li, an epidemiologist at McGill
University.
While past studies have looked at genetic changes, or mutations, in
sperm and eggs, which can be passed on to offspring, very few studies have
looked at somatic
mutations. These mutations, also called copy errors, can occur early in
fetal development, but because they aren't in the sex cells (the X or Y
chromosomes) of the fetus, they can't be passed on. Other studies have shown
that chemical modifications, or epiegnetic effects, can change which genes are expressed over the years, one factor
that renders twins not completely identical. Still, other work has shown that identical twins can have different gene mutations, but this study didn't determine
how often they occur.
To find out how often these mutations occur in early development, Li and
her colleagues studied the genomes of 92 pairs of identical twins and searched
hundreds of thousands of sites in their genomes for differences between twins
in base pairs, which are represented by letters that make up DNA. For
instance, one twin may carry an A at one point while another carries a C. The
researchers could only detect differences that would occur very early in fetal
development and would show up in most cells in the body.
They then calculated the frequency with which these mutations occurred.
Only two sets of twins had such mutations, which translates to a DNA change
occurring once for every 10 million to 10 billion bases that are copied every
time a cell divides. While that may seem like a high accuracy rate, cells in
the body divide trillions of times. So that would mean an average twin pair
carries 359 genetic differences that occurred early in development.
One limitation of the study is that they could only estimate the
mutation rate based on blood cells, but some cells in the body divide much more
frequently and so may rack up many more mutations. Other cells, like brain
cells, don't regenerate much and would probably remain stable. "Our DNA samples came from blood samples," Li told
LiveScience. "You need to define different rates in different
tissues."
Source: Live Science
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