7 results on '"Ephrem Mekonnen"'
Search Results
2. Genetic differentiation in East African ethnicities and its relationship with endurance running success.
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André L S Zani, Mateus H Gouveia, Marla M Aquino, Rodrigo Quevedo, Rodrigo L Menezes, Charles Rotimi, Gerald O Lwande, Collins Ouma, Ephrem Mekonnen, and Nelson J R Fagundes
- Subjects
Medicine ,Science - Abstract
Since the 1960s, East African athletes, mainly from Kenya and Ethiopia, have dominated long-distance running events in both the male and female categories. Further demographic studies have shown that two ethnic groups are overrepresented among elite endurance runners in each of these countries: the Kalenjin, from Kenya, and the Oromo, from Ethiopia, raising the possibility that this dominance results from genetic or/and cultural factors. However, looking at the life history of these athletes or at loci previously associated with endurance athletic performance, no compelling explanation has emerged. Here, we used a population approach to identify peaks of genetic differentiation for these two ethnicities and compared the list of genes close to these regions with a list, manually curated by us, of genes that have been associated with traits possibly relevant to endurance running in GWAS studies, and found a significant enrichment in both populations (Kalenjin, P = 0.048, and Oromo, P = 1.6x10-5). Those traits are mainly related to anthropometry, circulatory and respiratory systems, energy metabolism, and calcium homeostasis. Our results reinforce the notion that endurance running is a systemic activity with a complex genetic architecture, and indicate new candidate genes for future studies. Finally, we argue that a deterministic relationship between genetics and sports must be avoided, as it is both scientifically incorrect and prone to reinforcing population (racial) stereotyping.
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- 2022
- Full Text
- View/download PDF
3. An ancestral human genetic variant linked to an ancient disease: A novel association of FMO2 polymorphisms with tuberculosis (TB) in Ethiopian populations provides new insight into the differential ethno-geographic distribution of FMO2*1.
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Ephrem Mekonnen and Endashaw Bekele
- Subjects
Medicine ,Science - Abstract
The human FMO2 (flavin-containing monooxygenase 2) gene has been shown to be involved in innate immunity against microbial infections, including tuberculosis (TB), via the modulation of oxidative stress levels. It has also been found to possess a curious loss-of-function mutation (FMO2*1/FMO2*2) that demonstrates a distinctive differentiation in expression, function and ethno-geographic distribution. However, despite evidences of ethnic-specific genetic associations in the inflammatory profile of TB, no studies were done to investigate whether these patterns of variations correlate with evidences for the involvement of FMO2 in antimicrobial immune responses and ethnic differences in the distribution of FMO2 polymorphisms except for some pharmacogenetic data that suggest a potentially deleterious role for the functional variant (FMO2*1). This genetic epidemiological study was designed to investigate whether there is an association between FMO2 polymorphisms and TB, an ancient malady that remains a modern global health concern, in a sub-Saharan Africa setting where there is not only a relatively high co-prevalence of the disease and the ancestral FMO2*1 variant but also where both Mycobcaterium and Homo sapiens are considered to have originated and co-evolved. Blood samples and TB related clinical data were collected from ascertained TB cases and unrelated household controls (n = 292) from 3 different ethnic groups in Ethiopia. Latent Mtb infection was determined using Quantiferon to develop reliable TB progression phenotypes. We sequenced exonic regions of FMO2.We identified for the first time an association between FMO2 and TB both at the SNP and haplotype level. Two novel SNPs achieved a study-wide significance [chr1:171181877(A), p = 3.15E-07, OR = 4.644 and chr1:171165749(T), p = 3.32E-06, OR = 6.825] while multiple SNPs (22) showed nominal signals. The pattern of association suggested a protective effect of FMO2 against both active and latent TB with distinct genetic variants underlying the TB-progression pathway. The results were robust for population stratification. Haplotype-based tests confirmed the SNP-based results with a single haplotype bearing the ancestral-and-functional FMO2*1 "C" allele ("AGCTCTACAATCCCCTCGTTGCGC") explaining the overall association (haplotype-specific-p = 0.000103). Strikingly, not only was FMO2*1 nominally associated with reduced risk to "Active TB" (p = 0.0118, OR = 0.496) but it also does not co-segregate with the 5'-3' flanking top high-TB-risk alleles. The study provides an evidence for the existence of an evolutionary adaptation to an ancient disease based on an ancestral genetic variant acting in a haplotypic framework in Ethiopian populations.
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- 2017
- Full Text
- View/download PDF
4. Evidence of the interplay of genetics and culture in Ethiopia
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Neil Bradman, Nancy Bird, Saioa López, Sam Morris, Gavin Band, Lucy van Dorp, Tamiru Oljira, Endashaw Bekele, Mark G. Thomas, Ayele Tarekegn, Roger Blench, Garrett Hellenthal, Ephrem Mekonnen, López, Saioa [0000-0003-2936-4070], Band, Gavin [0000-0002-1710-9024], van Dorp, Lucy [0000-0002-6211-2310], Bird, Nancy [0000-0003-2596-874X], Oljira, Tamiru [0000-0002-8186-1667], Mekonnen, Ephrem [0000-0003-0416-649X], Thomas, Mark G. [0000-0002-2452-981X], Hellenthal, Garrett [0000-0002-5760-8020], Apollo - University of Cambridge Repository, and Thomas, Mark G [0000-0002-2452-981X]
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0301 basic medicine ,Male ,Population genetics ,Science ,Ethnic group ,General Physics and Astronomy ,Black People ,Ethnic Groups ,Big Five personality traits and culture ,631/208/457 ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,0302 clinical medicine ,Genetic similarity ,Geographical distance ,Cultural diversity ,Genetic variation ,Ethnicity ,Humans ,10. No inequality ,Social Factors ,Language ,African Continental Ancestry Group ,2. Zero hunger ,Multidisciplinary ,45 ,article ,Genetic Variation ,Linguistics ,General Chemistry ,Cultural Diversity ,631/208/728 ,Genetic differentiation ,Religion ,030104 developmental biology ,Geography ,Genetics, Population ,Haplotypes ,Evolutionary biology ,631/208/457/649 ,Multigene Family ,Genetic structure ,Female ,Ethiopia ,030217 neurology & neurosurgery - Abstract
The rich linguistic, ethnic and cultural diversity of Ethiopia provides an unprecedented opportunity to understand the level to which cultural factors correlate with–and shape–genetic structure in human populations. Using primarily new genetic variation data covering 1,214 Ethiopians representing 68 different ethnic groups, together with information on individuals’ birthplaces, linguistic/religious practices and 31 cultural practices, we disentangle the effects of geographic distance, elevation, and social factors on the genetic structure of Ethiopians today. We provide evidence of associations between social behaviours and genetic differences among present-day peoples. We show that genetic similarity is broadly associated with linguistic affiliation, but also identify pronounced genetic similarity among groups from disparate language classifications that may in part be attributable to recent intermixing. We also illustrate how groups reporting the same culture traits are more genetically similar on average and show evidence of recent intermixing, suggesting that shared cultural traits may promote admixture. In addition to providing insights into the genetic structure and history of Ethiopia, we identify the most important cultural and geographic predictors of genetic differentiation and provide a resource for designing sampling protocols for future genetic studies involving Ethiopians., Ethiopia is one of the most ethnically and culturally diverse countries. Here, the authors look at genetic and cultural variation in 1,214 Ethiopians to unravel the relationship between genetic admixture and cultural factors.
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- 2021
5. The genetic landscape of Ethiopia: diversity, intermixing and the association with culture
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van Dorp L, Bird N, Mark G. Thomas, Morris S, Saioa López, Endeshaw Bekele, Blench R, Garrett Hellenthal, Neil Bradman, Ephrem Mekonnen, Ayele Tarekegn, and Oljira T
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2. Zero hunger ,0303 health sciences ,Resource (biology) ,media_common.quotation_subject ,Ethnic group ,03 medical and health sciences ,0302 clinical medicine ,Geography ,Geographical distance ,Cultural diversity ,Genetic structure ,Genetic variation ,Economic geography ,030217 neurology & neurosurgery ,Selection (genetic algorithm) ,030304 developmental biology ,Diversity (politics) ,media_common - Abstract
SummaryThe rich linguistic, ethnic and cultural diversity of Ethiopia provides an unprecedented opportunity to understand the level to which cultural factors correlate with -- and shape -- genetic structure in human populations. Using primarily novel genetic variation data covering 1,214 Ethiopians representing 68 different ethnic groups, together with information on individuals’ birthplaces, linguistic/religious practices and 31 cultural practices, we disentangle the effects of geographic distance, elevation, and social factors upon shaping the genetic structure of Ethiopians today. We provide evidence of associations between social behaviours and increased genetic differences among present-day peoples. We show that genetic similarity is broadly associated with linguistic classifications, but indicate pronounced genetic similarity among groups from disparate language classifications that may in part be attributable to recent intermixing. We also illustrate how groups reporting the same culture traits are more genetically similar on average and show evidence of recent intermixing, suggesting how shared cultural traits may promote admixture. In addition to providing insights into the genetic structure and history of Ethiopia, these results identify the most important cultural and geographic proxies for genetic differentiation and provide a resource for designing sampling protocols for future genetic studies involving Ethiopians.
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- 2019
- Full Text
- View/download PDF
6. Tracing the route of modern humans out of Africa by using 225 human genome sequences from Ethiopians and Egyptians
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Yuan Chen, Toomas Kivisild, Stephan Schiffels, Ephrem Mekonnen, Petr Danecek, Luca Pagani, Tamiru Oljira, Deepti Gurdasani, Donata Luiselli, Chris Tyler-Smith, Neil Bradman, Marc Haber, Richard Durbin, Rosemary Ekong, Pierre Zalloua, Aylwyn Scally, Endashaw Bekele, Yali Xue, Pagani, Luca, Schiffels, Stephan, Gurdasani, Deepti, Danecek, Petr, Scally, Aylwyn, Chen, Yuan, Xue, Yali, Haber, Marc, Ekong, Rosemary, Oljira, Tamiru, Mekonnen, Ephrem, Luiselli, Donata, Bradman, Neil, Bekele, Endashaw, Zalloua, Pierre, Durbin, Richard, Kivisild, Tooma, and Tyler-Smith, Chris
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Human Migration ,Population ,Egypt, Ancient ,Molecular Sequence Data ,Black People ,Biology ,Coalescent theory ,03 medical and health sciences ,Genetic ,Principal Component Analysi ,Out of africa ,Report ,Genetics ,Haplotype ,Humans ,Genetics(clinical) ,education ,Genetics (clinical) ,History, Ancient ,030304 developmental biology ,African Continental Ancestry Group ,0303 health sciences ,education.field_of_study ,Genetic diversity ,Principal Component Analysis ,Base Sequence ,Geography ,Models, Genetic ,Human migration ,business.industry ,Genome, Human ,030305 genetics & heredity ,High-Throughput Nucleotide Sequencing ,Markov Chain ,Biological Evolution ,Markov Chains ,Haplotypes ,Evolutionary biology ,Homo sapiens ,Human genome ,Egypt ,Ethiopia ,business ,Human - Abstract
The predominantly African origin of all modern human populations is well established, but the route taken out of Africa is still unclear. Two alternative routes, via Egypt and Sinai or across the Bab el Mandeb strait into Arabia, have traditionally been proposed as feasible gateways in light of geographic, paleoclimatic, archaeological, and genetic evidence. Distinguishing among these alternatives has been difficult. We generated 225 whole-genome sequences (225 at 8× depth, of which 8 were increased to 30×; Illumina HiSeq 2000) from six modern Northeast African populations (100 Egyptians and five Ethiopian populations each represented by 25 individuals). West Eurasian components were masked out, and the remaining African haplotypes were compared with a panel of sub-Saharan African and non-African genomes. We showed that masked Northeast African haplotypes overall were more similar to non-African haplotypes and more frequently present outside Africa than were any sets of haplotypes derived from a West African population. Furthermore, the masked Egyptian haplotypes showed these properties more markedly than the masked Ethiopian haplotypes, pointing to Egypt as the more likely gateway in the exodus to the rest of the world. Using five Ethiopian and three Egyptian high-coverage masked genomes and the multiple sequentially Markovian coalescent (MSMC) approach, we estimated the genetic split times of Egyptians and Ethiopians from non-African populations at 55,000 and 65,000 years ago, respectively, whereas that of West Africans was estimated to be 75,000 years ago. Both the haplotype and MSMC analyses thus suggest a predominant northern route out of Africa via Egypt.
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- 2015
7. The African Genome Variation Project shapes medical genetics in Africa
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Gershim Asiki, Fasil Tekola-Ayele, Stephen Tollman, Dominic P. Kwiatkowski, Eleftheria Zeggini, Adebowale Adeyemo, Manjinder S. Sandhu, Luca Pagani, Ayesha A. Motala, Charles N. Rotimi, Deepti Gurdasani, Kalifa Bojang, Tommy Carstensen, Yali Xue, Elizabeth H. Young, Anatoli Kamali, Savita Karthikeyan, Tamiru Oljira, Neil Bradman, Rebecca N. Nsubuga, Katja Kivinen, Muminatou Jallow, Janet Seeley, Fatoumatta Sisay-Joof, Jennifer L. Asimit, Ephrem Mekonnen, Louise Iles, Endashaw Bekele, Graham R. S. Ritchie, Ananyo Choudhury, Pontiano Kaleebu, Rosemary Ekong, Konstantinos Hatzikotoulas, Martin O. Pollard, Fraser J. Pirie, Michèle Ramsay, Shane A. Norris, K Rockett, Ayo P. Doumatey, Cristina Pomilla, Ioanna Tachmazidou, Chris Tyler-Smith, Asimit, Jennifer [0000-0002-4857-2249], Kivinen, Katja [0000-0002-1135-7625], Sandhu, Manjinder [0000-0002-2725-142X], and Apollo - University of Cambridge Repository
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medicine.medical_specialty ,Asia ,Genetics, Medical ,Population genetics ,Biology ,Genome variation ,Risk Factors ,Genotype ,Genetic variation ,parasitic diseases ,medicine ,Humans ,Selection, Genetic ,Africa South of the Sahara ,Genetics ,Genetic diversity ,Multidisciplinary ,Genome, Human ,Haplotype ,Genetic Variation ,Genomics ,3. Good health ,Europe ,Evolutionary biology ,Africa ,Medical genetics ,Imputation (genetics) - Abstract
Given the importance of Africa to studies of human origins and disease susceptibility, detailed characterization of African genetic diversity is needed. The African Genome Variation Project provides a resource with which to design, implement and interpret genomic studies in sub-Saharan Africa and worldwide. The African Genome Variation Project represents dense genotypes from 1,481 individuals and whole-genome sequences from 320 individuals across sub-Saharan Africa. Using this resource, we find novel evidence of complex, regionally distinct hunter-gatherer and Eurasian admixture across sub-Saharan Africa. We identify new loci under selection, including loci related to malaria susceptibility and hypertension. We show that modern imputation panels (sets of reference genotypes from which unobserved or missing genotypes in study sets can be inferred) can identify association signals at highly differentiated loci across populations in sub-Saharan Africa. Using whole-genome sequencing, we demonstrate further improvements in imputation accuracy, strengthening the case for large-scale sequencing efforts of diverse African haplotypes. Finally, we present an efficient genotype array design capturing common genetic variation in Africa.
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- 2014
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