Author(s): Zanhua Yi, Nanibaa’ Garrison, Orit Cohen-Barak, Tatiana M. Karafet, Richard A. King, Robert P. Erickson, Michael F. Hammer, Murray H. Brilliant
Journal: American Journal of Human Genetics
Oculocutaneous albinism (OCA) is a genetically heterogeneous disorder. There are four known types of OCA: OCA1OCA4. The clinical manifestations of all types of OCA include skin and hair hypopigmentation and visual impairment. Although there are a few documented observations of high frequency of albinism among Native Americans, including the Hopi, Zuni, Kuna, Jemez, Laguna, San Juan, and Navajo, no causative molecular defect has been previously reported. In the present study, we show that albinism in one Native American population, the Navajo, is caused by a LINE-mediated 122.5-kilobase deletion of the P gene, thus demonstrating that albinism in this population is OCA2. This deletion appears to be Navajo specific, because this allele was not detected in 34 other individuals with albinism who listed other Native American origins, nor has it been reported in any other ethnic group. The molecular characterization of this deletion allele allowed us to design a three-primer polymerase chain reaction system to estimate the carrier frequency in the Navajo population by screening 134 unrelated normally pigmented Navajos. The carrier frequency was found to be ?4.5%. The estimated prevalence of OCA2 in Navajos is between ?1 per 1,500 and 1 per 2,000. We further estimate that this mutation originated 4001,000 years ago from a single founder.
Source Link: http://dx.doi.org/10.1086/345380
Peoples: Hopi, Jemez, Kuna, Laguna, Navajo, San Juan, and Zuni | Places: North America | Topics: Oculocutaneous Albinism Type 2 | DNA Type: Autosomal DNA