Evidence map›Paper›PMID 18245828›Full record

ArticleGenetics2008

Selection in the making: a worldwide survey of haplotypic diversity around a causative mutation in porcine IGF2.

A Ojeda, L-S Huang, J Ren, A Angiolillo, I-C Cho, H Soto, C Lemús-Flores, S M Makuza, J M Folch, M Pérez-Enciso

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 49 citations in OpenAlex.

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  13. The genetic structure of domestic rabbits.Molecular biology and evolution · 2011
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  19. Genome-wide scans for footprints of natural selection.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2010
    Review
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

10 authors at 7 institutions in 6 countries.

A OjedaInstitut Català de Recerca i Estudis Avançats, 08010 Barcelona, Spain.
L-S Huang
J Ren
A Angiolillo
I-C Cho
H Soto
C Lemús-Flores
S M Makuza
J M Folch
M Pérez-Enciso
Jiangxi Agricultural University · CNUniversitat Autònoma de Barcelona · ESInstitució Catalana de Recerca i Estudis Avançats · ESUniversidad Autónoma de Nayarit · MXUniversidad de Costa Rica · CRUniversity of Molise · ITUniversity of Zimbabwe · ZW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Domestic species allow us to study dramatic evolutionary changes at an accelerated rate due to the effectiveness of modern breeding techniques and the availability of breeds that have undergone distinct selection pressures. We present a worldwide survey of haplotype variability around a known causative mutation in porcine gene IGF2, which increases lean content. We genotyped 34 SNPs spanning 27 kb in 237 domestic pigs and 162 wild boars. Although the selective process had wiped out variability for at least 27 kb in the haplotypes carrying the mutation, there was no indication of an overall reduction in genetic variability of international vs. European local breeds; there was also no evidence of a reduction in variability caused by domestication. The haplotype structure and a plot of Tajima's D against the frequency of the causative mutation across breeds suggested a temporal pattern, where each breed corresponded to a different selective stage. This was observed comparing the haplotype neighbor-joining (NJ) trees of breeds that have undergone increasing selection pressures for leanness, e.g., European local breeds vs. Pietrain. These results anticipate that comparing current domestic breeds will decisively help to recover the genetic history of domestication and contemporary selective processes.

Indexed as

Genetic VariationHaplotypesSelection, GeneticAnimalsBase SequenceGene FrequencyInsulin-Like Growth Factor IILinkage DisequilibriumMolecular Sequence DataMutationPhylogenyPolymorphism, Single NucleotideSequence AlignmentSus scrofaInsulin-Like Growth Factor II

Identifiers

PMID18245828
PMCPMC2278092
OpenAlexW2096303074

What OpenQuestion holds

Textmetadata
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.