Why Identical Twins Are Not Always Identical

Source:  Why Identical Twins Are Not Always Identical    Tag:  complete heterochromia
I found this post by Kevin Mitchell in his blog Wiring the Brain to be fascinating. It explains why identical twins are not always identical:
... these studies also highlight the limits of genetic determinism, which is especially evident in comparisons of monozygotic (identical) twins, who share all their genetic inheritance in common. Though they are obviously much more like each other in psychological traits than people who are not related to each other, they are clearly NOT identical to each other for these traits. For example, if one twin has a diagnosis of schizophrenia, the chance that the other one will also suffer from the disorder is about 50% - massively higher than the population prevalence of the disorder (around 1%), but also clearly much less than 100%.

What is the source of this extra variance? What forces make monozygotic twins less identical? I have argued previously that random variation in the course of development is a major contributor. The developmental programme that specifies brain connectivity is less like a blueprint than a recipe (a recipe without a cook) – an incredibly complicated set of processes carried out by mindless biochemical algorithms mediated by local interactions between billions of individual components. As each of these processes is subject to some level of “noise” at the molecular level, it is not surprising that the outcome of this process varies considerably, even between monozygotic twins.

While such developmental variation can be referred to as “non-genetic”, a new study suggests that one important component of this variation may be genetic after all, just not inherited. Mutations can be passed on from parents to offspring or arise during generation of sperm or eggs and thus be inherited, but they can also arise any time DNA is replicated. So, each time a cell divides as an embryo grows and develops, there is a very small chance of new mutations being introduced. These “somatic” mutations (meaning ones that happen in the body and not in the germline) will be inherited by all the cells that are descendants of that new cell and so will be present in some fraction of the final cells of the individual. Mutations arising earlier in development will be inherited by more cells than those arising later.

Each person will therefore be a mosaic of cells with slightly different genetic make-up. The vast majority of such mutations will not have any effect of course (with the obvious exception of those that cause dysregulation of cellular differentiation and result in cancer). But sometimes a new mutation will affect a trait and cause a detectable difference. The most obvious examples are in genes affecting hair or eye colour – where a patch of hair may be a different colour, or the two eyes may be different colours.

But what if the mutations in question are linked to a psychiatric disorder? If such a mutation arises early in the development of the brain and is therefore inherited by many of the cells in the brain then this could lead to the psychiatric disorder, just as if the mutation had been inherited in a germ cell.

A new study adds to the evidence that such mutations do indeed occur at an appreciable frequency and may help explain the discordance in phenotype between pairs of twins where one has schizophrenia and the other does not. The authors analysed the DNA from blood cells of pairs of twins discordant for schizophrenia and their parents. They were looking for two different kinds of mutation: ones that changes the identity of a single base of DNA (one letter of the genetic code to another), called point mutations, and ones that delete or duplicate whole chunks of chromosomes, called copy number variants, or CNVs.

As expected, they were able to detect both inherited mutations (present in one of the parents) and de novo mutations (present in both twins but not in the blood cells of either parent). What is more remarkable though, is that they also detected de novo mutations present in the blood cells of one twin but not the other – lots of them. About 1,000 point mutations and 2-3 new CNVs not shared by the other twin. The implication is that these mutations arose during the somatic development of one twin. They identify a couple CNVs in the twins affected by schizophrenia, raising the (very speculative) possibility that those mutations may contribute to the development of the disorder. It will obviously require a lot more work to test that specific hypothesis.
All of this is fascinating, but especially interesting is that this effect is visible at the macro level. You can see it with the condition heterochromia iridum (the two eyes having different colours).

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