In 1909, Danish botanist Wilhelm Johanssen coined the term "gene," describing it as the mechanism that allowed children to inherit traits from their parents. By the 1960s, that definition had taken a turn for the specific: Genes were the
DNA code used to make proteins. Ten years ago the
Human Genome Project produced the first draft of our genetic blueprints--but scientists weren't able to rejoice in their complete knowledge of the secrets that lie tucked inside our cells, because the story was already unravelling.
In the 1980s and 1990s, researchers found that only about 1.2 percent of our DNA codes for proteins: some called these other parts "junk." A 1980
review paper (pdf) by Leslie Orgel and Francis Crick calls this DNA "the ultimate parasite." Yet in this apparent junk-pile, researchers continue to find functioning scraps.
It seems that as we probe deeper into the human genome, we realize how much we have left to learn. For example, researchers have discovered that some sections of our DNA are like genetic switchboards. Molecules attaching to these sections can turn on or shut off protein-making genes, and malfunctions there may be responsible for conditions ranging from
depression to
obesity. What's more, these switches can be flipped after birth, as the attaching molecules can be added or removed by environmental factors. For example,
Michael Meaney, a researcher at McGill University, recently
found that how often young rats' mothers licked them changed what molecules attached to their DNA--and possibly in turn their stress levels. The ongoing
Human Epigenome Project hopes to study these DNA accoutrements and their effects.