Evidence map›Paper›PMID 24736786›Full record

ArticleHeredity2014

Genome-wide analysis reveals the ancient and recent admixture history of East African Shorthorn Zebu from Western Kenya.

M N Mbole-Kariuki, T Sonstegard, A Orth, S M Thumbi, B M de C Bronsvoort, H Kiara, P Toye, I Conradie, A Jennings, K Coetzer and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Heredity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 71 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 9 institutions in 5 countries.

M N Mbole-KariukiEcology and Evolution, School of Life Sciences, University of Nottingham, Nottingham, UK.
T SonstegardUnited States Department of Agriculture, Agriculture, Agricultural Research Services, Bovine Functional Genomics Laboratory, Beltsville, MD, USA.
A OrthInternational Livestock Research Institute, Nairobi, Kenya.
S M ThumbiCentre for Immunity, Infection and Evolution, Ashworth Laboratories, University of Edinburgh, Edinburgh, UK.
B M de C BronsvoortThe Roslin Institute, Easter Bush, University of Edinburgh, Edinburgh, UK.
H KiaraInternational Livestock Research Institute, Nairobi, Kenya.
P ToyeInternational Livestock Research Institute, Nairobi, Kenya.
I ConradieDepartment of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, South Africa.
A JenningsThe Roslin Institute, Easter Bush, University of Edinburgh, Edinburgh, UK.
K CoetzerDepartment of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, South Africa.
M E J WoolhouseCentre for Immunity, Infection and Evolution, Ashworth Laboratories, University of Edinburgh, Edinburgh, UK.
O HanotteEcology and Evolution, School of Life Sciences, University of Nottingham, Nottingham, UK.
M TapioMTT FI-31600, Jokioinen, Finland.
International Livestock Research Institute · KEUniversity of Edinburgh · GBUniversity of Nottingham · GBAgricultural Research Service · USAgrifood Research Finland · FICentre for Immunity, Infection and Evolution · GBOnderstepoort Veterinary Academic Hospital · ZARoslin Institute · GBUniversity of Pretoria · ZA

Funding

Biotechnology and Biological Sciences Research Council BBS/E/D/20211550Biotechnology and Biological Sciences Research Council BBS/E/D/20211554Wellcome Trust 07995Wellcome Trust 095831
6 · The paper itself

Abstract

The Kenyan East African zebu cattle are valuable and widely used genetic resources. Previous studies using microsatellite loci revealed the complex history of these populations with the presence of taurine and zebu genetic backgrounds. Here, we estimate at genome-wide level the genetic composition and population structure of the East African Shorthorn Zebu (EASZ) of western Kenya. A total of 548 EASZ from 20 sub-locations were genotyped using the Illumina BovineSNP50 v. 1 beadchip. STRUCTURE analysis reveals admixture with Asian zebu, African and European taurine cattle. The EASZ were separated into three categories: substantial (⩾12.5%), moderate (1.56%<X<12.5%) and non-introgressed (⩽1.56%) according to the European taurine genetic proportion. The non-European taurine introgressed animals (n=425) show an unfluctuating zebu and taurine ancestry of 0.84±0.009 s.d. and 0.16±0.009 s.d., respectively, with significant differences in African taurine (AT) and Asian zebu backgrounds across chromosomes (P<0.0001). In contrast, no such differences are observed for the European taurine ancestry (P=0.1357). Excluding European introgressed animals, low and nonsignificant genetic differentiation and isolation by distance are observed among sub-locations (Fst=0.0033, P=0.09; r=0.155, P=0.07). Following a short population expansion, a major reduction in effective population size (Ne) is observed from approximately 240 years ago to present time. Our results support ancient zebu × AT admixture in the EASZ population, subsequently shaped by selection and/or genetic drift, followed by a more recent exotic European cattle introgression.

Indexed as

Evolution, MolecularGenomeAnimalsCattleGenotypeKenyaMaleMicrosatellite Repeats

Identifiers

PMID24736786
PMCPMC4181064
OpenAlexW2154804764

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.