Distribution of corticotropin-releasing hormone promoter polymorphism in different ethnic groups: evidence for natural selection in human populations

Citation
Cgo. Baerwald et al., Distribution of corticotropin-releasing hormone promoter polymorphism in different ethnic groups: evidence for natural selection in human populations, IMMUNOGENET, 49(10), 1999, pp. 894-899
Citations number
28
Categorie Soggetti
Immunology
Journal title
IMMUNOGENETICS
ISSN journal
00937711 → ACNP
Volume
49
Issue
10
Year of publication
1999
Pages
894 - 899
Database
ISI
SICI code
0093-7711(199909)49:10<894:DOCHPP>2.0.ZU;2-W
Abstract
The regulatory region of the corticotropin-releasing hormone (CRH) is highl y conserved across species and plays a crucial role in the response of the organism to stress. Release of CRH initiates a cascade of events leading to the release of cortisol and the regulation of inflammatory and immune even ts, In this report we describe polymorphisms in the 5' regulatory region of the CRH gene in humans, We studied the distribution of CRH alleles in thre e different African populations, in white UK Caucasoids, and in a Chinese p opulation. In the African and UK populations we found three new polymorphis ms which cosegregated, resulting in two alleles, A1 and A2. Gene frequencie s for A1 and A2 were extremely divergent between the African and the UK pop ulations. The African A1 frequency ranged from 0.27-0.3, while the UK Cauca soid frequency was 0.9. Compound alleles could be assigned by taking into a ccount the previously described biallelic polymorphism at position 225 in t he CRH promoter. The A2B1 compound allele is the commonest in contemporary African human populations (allele frequency range 0.44-0.61) and was the on ly allele observed in a population of chimpanzees from Sierra Leone. Wright 's F-ST for the A2B1 allele over the four sampled populations was 0.612, a value exceeded in human populations only by loci which have apparently been subject to natural selection. Taken together, these findings support A2B1 as the ancestral allele and suggest that the CRH genomic region may have be en subject to strong disruptive selection throughout human evolution.