The lineage of domesticated chickens can be traced from red junglefowl in southeast Asia. But hanging around humans for thousands of years has transformed this animal into the familiar egg-laying feathered fowl we know and love. As a consequence of domestication and accompanying humans in their travels, many chicken breeds can be found worldwide. Researchers decided to look at the genetics of breeds from two very different environments: Northern Europe and Africa. These chickens have lived for numerous generations in their locales and thus would be subject to the local climate conditions. These environmental stresses would likely exert selective pressures on the poultry so Fleming et al. were interested in see what differences might exist. They started by genotyping single nucleotide polymorphisms (SNPs) from 718 individuals of indigenous breeds (375 from Africa and 343 from Europe) encompassing five European countries and nine African countries. After some quality control of the data, only 634 birds had acceptable data dividing into 315 African samples and 319 European samples.
These genotype data were then subjected to various software analyses. Analyzing the data by temperature profiles and genotype showed that the Northern European chickens clustered together both by country and continent, and the same held true for the African chickens. Taking both genotype data sets and looking for regions of increasing genomic differentiation, chromosomes 4, 17 and 27 showed peaks during analysis. Examining the gene ontology of the region of chromosome 4, which showed higher allele frequency in the Northern European chickens, included functions related to developmental pathways and immune response. The chromosome 17 region had genes involved with calcium sequestration and blood vessel creation. For chromosome 27, the possible region under selection included genes for feather keratin and nearby a recently discovered quantitative trait locus (QTL) for body temperature under heat stress conditions.
Using these various computed selection signatures, Fleming et al. analyzed the downstream gene ontology from the genes found near the significant SNVs in the various chromosomes. For the chickens indigenous to Africa, apoptosis, immune function and homeostasis processes were altered significantly whereas chickens indigenous to Northern Europe had changes in pathways involved in cell adhesion and angiogenesis.
Additional analysis on gene diversity and environmental factors (precipitation and temperature) on the two chicken populations found selective associations with both factors. Some of these loci under pressure also overlapped with those that were significant in selection signatures analyses including chromosomes 25, 26 and 27 for African chickens and chromosomes 2, 3 and 20 for Northern European chickens.
What have Fleming et al. discovered with their analysis of African and Northern European chickens? Their results indicate that there are different regions of the chicken genome under selection and that those areas of diversity are affected by the climate in which the breed of poultry has existed. African chickens seem to have strong selection markers on chromosome 27, suggesting mechanisms that allow the birds to tolerate heat from homeostatic functioning to angiogenesis. Northern European chickens showed selection in loci on chromosomes 2 and 3 that affect metabolism and feathering, two processes that can affect how the animal keeps warm in the colder climate. Not only will I look at my flock with new appreciation for their adaptations but know it is appropriate that that most of my chickens are classified as American Large Fowl breeds, ones likely adapted for the environmental conditions in my locale.
Reference
Fleming, D.S., Weigend, S., Simianer, H., Weigend, A., Rothschild, M., Schmidt, C., Ashwell, C., Persia, M., Reecy, J. and Lamont, S.J. (2017) Genomic comparison of indigenous African and Northern European chickens reveals putative mechanisms of stress tolerance related to environmental selection pressure. G3 (Bethesda) 7, 1525–37. doi: 10.1534/g3.117.041228.
Sara Klink
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