During reprogramming in the early zygote, the methylation is removed from most of our DNA. But IAP retrotransposons are an exception to this. The reprogramming machinery has evolved to skip these rogue elements and leave the DNA methylation marks on them. This keeps the retrotransposons in an epigenetically repressed state. This has probably evolved as a mechanism to reduce the risk that potentially dangerous IAP retrotransposons will get accidentally re-activated.
This is relevant because the two best-studied examples of transgenerational inheritance of non-genetic features are the
We met other examples of transgenerational inheritance of acquired characteristics in Chapter 6, including the effects of nutrition on subsequent generations, and the transgenerational effects of environmental pollutants such as vinclozolin. Researchers are exploring the hypothesis that these environmental stimuli create epigenetic changes in the chromatin of the gametes. These alterations are probably in regions that are protected from reprogramming during early development after the egg and sperm fuse.
Like John Gurdon, Azim Surani has continued to work highly productively in a field that he pioneered. His work has been focused on how and why eggs and sperm barcode their DNA so that a molecular memory is passed on to the next generation. A large amount of Azim Surani’s initial pioneering work was dependent on manipulating mammalian nuclei by using tiny pipettes to transfer them between cells. Technically, this is a refined version of the methods that John Gurdon used so successfully fifteen years earlier. It’s oddly pleasing to consider that Professor Surani is now based at the research institute in Cambridge that is named after Professor Gurdon, and that they frequently bump into each other in the corridors and the coffee room.
Chapter 8. The Battle of the Sexes
Nobody will ever win the Battle of the Sexes. There’s just too much fraternising with the enemy.
The laboratory stick insect
Stick insects frequently reproduce this way. They are using a mechanism known as parthenogenesis, from the Greek for ‘virgin birth’. Females lay fertile eggs without ever mating with a male, and perfectly healthy little stick insects emerge from these eggs. These insects have evolved with special mechanisms to ensure that the offspring have the correct number of chromosomes. But these chromosomes all came from the mother.
This is very different from mice and humans, as we saw in the last chapter. For us and our rodent relatives, the only way to generate live young is by having DNA from both a mother and a father. It’s tempting to speculate that stick insects are highly unusual but they’re not. We mammals are the exceptions. Insects, fish, amphibians, reptiles and even birds all have a few species that can reproduce parthenogenetically. It’s we mammals who can’t. It’s our class in the animal kingdom which is the odd one out, so it makes sense to ask why this is the case. We can begin by looking at the features which are found only in mammals. Well, we have hair, and we have three bones in our middle ear. Neither of these characteristics is found in the other classes, but it seems unlikely these are the key features that have led us to abandon virgin birth. For this issue there is a much more important characteristic.
The most primitive examples of mammals are the small number of creatures like the duck-billed platypus and the echidna, which lay eggs. After them, in terms of reproductive complexity, are the marsupials such as the kangaroo and the Tasmanian devil, which give birth to very under-developed young. The young of these species go through most of their developmental stages outside the mother’s body, in her pouch. The pouch is a glorified pocket on the outside of the body.