Evidence map›Paper›PMID 26863414›Full record

ArticlePloS one2016

Dietary Variation and Evolution of Gene Copy Number among Dog Breeds.

Taylor Reiter, Evelyn Jagoda, Terence D Capellini

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

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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

3 authors.

Taylor ReiterHuman Evolutionary Biology, Harvard University, 11 Divinity Avenue, Cambridge, MA, 02138, United States of America.
Evelyn JagodaHuman Evolutionary Biology, Harvard University, 11 Divinity Avenue, Cambridge, MA, 02138, United States of America.
Terence D CapelliniHuman Evolutionary Biology, Harvard University, 11 Divinity Avenue, Cambridge, MA, 02138, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prolonged human interactions and artificial selection have influenced the genotypic and phenotypic diversity among dog breeds. Because humans and dogs occupy diverse habitats, ecological contexts have likely contributed to breed-specific positive selection. Prior to the advent of modern dog-feeding practices, there was likely substantial variation in dietary landscapes among disparate dog breeds. As such, we investigated one type of genetic variant, copy number variation, in three metabolic genes: glucokinase regulatory protein (GCKR), phytanol-CoA 2-hydroxylase (PHYH), and pancreatic α-amylase 2B (AMY2B). These genes code for proteins that are responsible for metabolizing dietary products that originate from distinctly different food types: sugar, meat, and starch, respectively. After surveying copy number variation among dogs with diverse dietary histories, we found no correlation between diet and positive selection in either GCKR or PHYH. Although it has been previously demonstrated that dogs experienced a copy number increase in AMY2B relative to wolves during or after the dog domestication process, we demonstrate that positive selection continued to act on amylase copy number in dog breeds that consumed starch-rich diets in time periods after domestication. Furthermore, we found that introgression with wolves is not responsible for deterioration of positive selection on AMY2B among diverse dog breeds. Together, this supports the hypothesis that the amylase copy number expansion is found universally in dogs.

Indexed as

Adaptor Proteins, Signal TransducingAnimal FeedAnimalsCarbohydrate MetabolismComparative Genomic HybridizationDietDNA Copy Number VariationsDogsEvolution, MolecularGene DosageMixed Function OxygenasesPancreatic alpha-AmylasesAdaptor Proteins, Signal TransducingMixed Function OxygenasesPancreatic alpha-Amylases

Identifiers

PMID26863414
PMCPMC4749313

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Registered trials

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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.