A modern human and a Neanderthal one |
Some parts of non-African genomes are totally devoid of Neanderthal DNA, but other regions abound with it, including those containing genes that affect our skin and hair. This hints that the Neanderthal gene versions conferred some benefit, and were kept during evolution.
The fact that Neanderthal DNA is totally absent from other stretches of the modern non-African genome suggests that their versions of the genes in these regions would have caused problems in modern humans, and were weeded out by natural selection.
A Neanderthal and his skull |
If a fragment of DNA is shared by Neanderthals and non-Africans, but not Africans or other primates, it is likely to be a Neanderthal heirloom. Also, Neanderthal sequences are typically inherited in large batches, since they were imported into the modern human genome relatively recently and have not had time to break apart.
In the Science study, Akey and Benjamin Vernot, both of the University of Washington in Seattle, used similar statistical features to search for Neanderthal DNA in the genomes of 665 living people—but they initially did so without the Neanderthal genome as a reference. They still managed to identify fragments that collectively amount to 20 percent of the full Neanderthal genome.
More information: Nature
Neanderthal Influence on Skin, Hair, Common Diseases
Despite their different approaches, both teams converged on similar results. They both found that genes involved in making keratin—the protein found in our skin, hair, and nails—are especially rich in Neanderthal DNA.
For example, the Neanderthal version of the skin gene POU2F3 is found in around 66 percent of East Asians, while the Neanderthal version of BNC2, which affects skin color, among other traits, is found in 70 percent of Europeans.
Comparison: Modern Humans and Neanderthals |
Neanderthals had been in these environments for hundreds or thousands of years, says Sankararaman. As modern human ancestors moved into these areas, one way to quickly adapt would be to get genes from the Neanderthals.
Unfortunately, skin and hair do so many things that it's hard to speculate on what specifically that adaptive trait was, says Akey.
Sankararaman also found Neanderthal variants in genes that affect the risk of several diseases, including lupus, biliary cirrhosis, Crohn's disease, and type 2 diabetes. The significance of these sequences is even less clear.
More information: New Historian
Both teams found that non-African genomes have large continuous deserts that are totally devoid of Neanderthal DNA. These regions include genes such as FOXP2, which is involved in motor coordination and could play an important role in human language and speech.
The Neanderthal-poor deserts are especially big in the X chromosome, and include genes that are specifically activated in testes. This hints that some Neanderthal genes may have reduced the fertility of male modern humans and were eventually lost. However, Hawks cautions that this probably happened over hundreds of generations—it was very unlikely that the sons of Neanderthals and modern humans were obviously infertile.
DNA Hints at Other Mystery Humans
A Neanderthal man |
And Akey's work shows that it may even be possible to partially reconstruct the genomes of unknown groups of ancient humans without any prehistoric DNA samples.
It is becoming increasingly clear that the Pleistocene was awash with many different groups of early humans, hooking up with each other to various degrees. Recent studies, for instance, have found tantalizing hints of unknown groups from Asia and Africa that left genes in Denisovans and modern humans, respectively. Akey's method could give us our first glimpse at these mystery humans.
If there is no fossil evidence and potentially never will be, this will be the only way of finding out about groups that were important in human history, he added.
If we turn to palaeontology to tell us about our biological evolution it is to prehistory that we look for evidence of the evolution of specifically human patterns of behaviour.
John G. D. Clark
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