Where's the evolution?
But how did scientists get from a "golden" fish to human ethnic groups, and what does this all have to do with evolution? The answer relies upon the evolutionary relationship between humans and fish and helps illuminate how and why human skin color differences evolved in the first place.
Though the Human Genome Project has revealed the string of three billion base pairs that represents our genetic sequence, we still know relatively little about the meaning of that sequence. However, because all life on Earth shares common ancestors and because we and other species have inherited many of the same genes from those ancestors, we can learn more about our own genome by studying the genes of other species. For example, researchers can experimentally manipulate a gene in another organism (such as a zebrafish) in order to figure out how the gene works and then look for the homologous gene in humans — the version of the gene that humans also inherited from an ancestor we share with the study organism.
That strategy was the approach that the Penn State researchers took when they began studying the zebrafish. The common ancestor of humans and zebrafish swam in the oceans more than 400 million years ago. Despite the enormous length of time that separates those two lineages, they share many genes, such as this recently-discovered pigmentation gene. The zebrafish and human versions of the gene are about 70% identical. In zebrafish, the gene codes for dark stripes — but by breaking the gene and cutting short the protein that it produces, researchers can engineer a golden-hued zebrafish without dark stripes. The same gene was also discovered in the human genome, where it explains much of the difference in skin color between African and European descendents. Interestingly, the gene variants that correspond to dark and light skin in humans are remarkably similar to one another — they differ by just one base pair!
But how did different ethnic groups wind up with these different versions of the pigmentation gene? Research suggests that more than 100,000 years ago, the earliest humans lived in Africa and carried the "G" allele, which causes lots of melanin to be present in skin cells and hence, dark skin. Melanin absorbs UV rays from the sun and controls the amount of UV radiation that penetrates our skin. Our bodies need some UV radiation (to build the essential vitamin, vitamin D) but not too much (because UV radiation can damage the skin and destroy another essential vitamin, folate). In the sun-drenched environs of Africa, dark skin was advantageous, preventing UV rays from doing too much damage, while allowing in enough UV to synthesize vitamin D. In that environment, individuals born with a mutant version of the gene associated with less melanin and lighter skin would probably have had poor health and low reproductive success.
Many biologists hypothesize that between 55,000 and 85,000 years ago, humans began to migrate out of Africa. Some of them wound up living in the colder, darker climes of Europe. There, too much UV radiation was not a problem, but too little UV to synthesize vitamin D probably was. At some point either before or after the migration out of Africa, a mutation occurred in one of the ancestors of modern Europeans. This mutation was tiny, changing just a single base, but it caused much less melanin to be present in the skin of those who carried the mutation. This was the "A" allele. Among the new Europeans, this allele likely had an advantage over the "G" allele. Individuals carrying the "A" allele had less melanin, which allowed more UV light to penetrate their skin, which could have allowed them to synthesize vitamin D better than those carrying only the "G" allele. These "A"-carrying individuals had increased reproductive success in their sun-poor environment, and via natural selection, the "A" allele spread throughout the European population. Meanwhile, among Africans, the "G" allele continued to be advantageous and to maintain its majority there.
The discovery of this pigmentation gene has helped us piece together a more complete picture of the evolutionary changes that underlie skin color differences between human ethnic groups. It suggests that a great deal of the skin color difference that has delineated the boundaries of social tensions for much of recorded history can be traced back to a tiny genetic change that allowed humans to better survive and reproduce in particular environments.
This discovery also highlights the fundamental similarity of all humans. Skin color, it turns out, really is skin deep; at a genetic level, the skin color difference between a European descendent and an African descendent might be largely influenced by a single base pair difference in a genome composed of three billion base pairs. However, neither does this single gene tell the whole story. For example, many East Asians carry the "G" allele and yet have light-colored skin. Why? We don’t know, but it is probably due to many other undiscovered genes. And though, on average, people who carry only the "A" allele have lighter skin than those who carry only the "G" allele, there is a huge overlap in skin color between the groups — so knowing which alleles an individual carries will not let you predict with much certainty the shade of his or her skin. It is clear that the concept of "race" is more a sociological construct than a biological one, and that many genes and environmental factors influence skin color. As we learn more about these genes, we will learn more about our own evolutionary history as a species.
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| Variation in humans, demonstrated by some members of the University of California faculty. |
Finally, methods used to discover this pigmentation gene reveal the deep connections between our own species and others that have lived over the approximately 3.5 billion years of life's history. Studying the zebrafish, for example, led to discoveries about our own evolutionary history and genetic variation. And because of the common ancestry of all life on Earth, other species (as different from us as they may seem) represent our evolutionary cousins and can teach us about ourselves and our history.
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For teachers
Discussion and extension questions:
- How is the zebrafish pigmentation gene relevant to the human pigmentation gene discussed here?
- What is a homology? Describe an example of a homology from the article above. Describe an example of a homology NOT mentioned in the article above.
- List some ways in which melanin could be helpful for human survival and reproduction. List some ways in which melanin could be bad for human survival and reproduction.
- In what circumstances is the "A" allele advantageous for humans? In what circumstances is the "G" allele advantageous for humans? Is one better than the other? Explain why or why not.
- Review some background information on natural selection. Imagine that in the ancestral European population, the "G" allele is common and just a few people carry the mutant "A" version of the gene. Explain how the allele frequencies of "A" and "G" would have changed over many generations in the sun-poor environment of Europe. Make sure to include the concepts of variation, selection, and inheritance in your explanation.
Related lessons and teaching resources:
References
- Biello, D. (2005, December 16). Researchers identify human skin color gene. Scientific American.
Retrieved January 17, 2006 from Scientific American
- Jablonski, N. G., and Chaplin, G. (2000). The evolution of human skin coloration. Journal of Human Evolution. 39: 57-106.
- Lamason, R. L., Mohideen, M. P. K., Mest, J. R., Wong, A. C., Norton, H. L., Aros, M. C., et al. (2005, December 16). SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science. 310:1782-1786.
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