Skin Pigmentation

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Skin pigmentation in modern humans is an adaptation to ultraviolet radiation. The most darkly pigmented skin is found among people living at or near the equator; the most lightly pigmented skin is found among people living above 45N latitude. The primary pigment in human skin is melanin, mostly in the form of the very dark brown eumelanin. Yellow-red pheomelanin is present in human skin to varying degrees, and is most obvious as the pigment causing freckles in people with very lightly pigmented skin. Eumelanin is a superior natural sunscreen with abilities to absorb wavelengths of visible and ultraviolet radiation. Darkly pigmented skin with high concentrations of eumelanin confers protection against high levels of both ultraviolet A (UVA=315-345 nm) and ultraviolet B (UVB=280-315 nm) radiation. Ultraviolet radiation is mostly harmful to humans because it damages DNA and breaks down folate, a B vitamin necessary for DNA synthesis and cell division.

The earliest members of Homo sapiens living in eastern and northeastern Africa were darkly pigmented, and genetic evidence indicates that variation in one of the primary genes controlling eumelanin production, the melanocortin 1 receptor (MC1R), was lost as the result of a selective sweep about 1.2 myr. Human dispersal into higher latitudes with lower levels of UVR was associated with positive selection for depigmentation. Although UVR is mostly harmful, UVB (optimally at 297 nm) initiates the production of vitamin D in the skin from a cholesterol-like precursor. Vitamin D is required for absorption of calcium and the growth and maintenance of a healthy skeleton; it is also important for normal development and functioning of the immune system and brain. Positive selection for depigmentation was driven by the importance of maintaining vitamin D photosynthesis in the skin under conditions of reduced UVB at higher latitudes. Evolution of depigmented skin occurred at least twice in Homo sapiens, in both the ancestors of modern northern Europeans and eastern Asians.

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 (Ito 2003; Jablonski and Chaplin 2000; Lamason et al. 2005; Makova and Norton 2005; Norton et al. 2007; Rogers et al. 2004; Thody et al. 1991)
 
Ito S (2003) A chemist's view of melanogenesis. Pigment Cell Res 16:230-236
Jablonski NG, Chaplin G (2000) The evolution of human skin coloration. Journal of Human Evolution 39(1):57-106
Lamason RL, Mohideen M-APK, Mest JR, Wong AC, Norton HL, Aros MC, Jurynec MJ, Mao X, Humphreville VR, Humbert JE, Sinha S, Moore JL, Jagadeeswaran P, Zhao W, Ning G, Makalowska I, McKeigue PM, O'Donnell D, Kittles R, Parra EJ, Mangini NJ, Grunwald DJ, Shriver MD, Canfield VA, Cheng KC (2005) SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310(5755):1782-1786
Makova K, Norton HL (2005) Worldwide polymorphism at the MC1R locus and normal pigmentation variation in humans. Peptides 26(10):1901-1908
Norton HL, Kittles RA, Parra E, McKeigue P, Mao X, Cheng K, Canfield VA, Bradley DG, McEvoy B, Shriver MD (2007) Genetic evidence for the convergent evolution of light skin in Europeans and East Asians. Molecular Biology and Evolution 24(3):710-722
Rogers AR, Iltis D, Wooding S (2004) Genetic variation at the MC1R locus and the time since loss of human body hair. Current Anthropology 45(1):105-124
Thody AJ, Higgins EM, Wakamatsu K, Ito S, Burchill SA, Marks JM (1991) Pheomelanin as well as eumelanin is present in human epidermis. Journal of Investigative Dermatology 97(2):340-344