Evidence map›Paper›PMID 33650783›Full record

ArticleMolecular genetics & genomic medicine2021

Worldwide variation of the COL14A1 gene is shaped by genetic drift rather than selective pressure.

Carla M Calò, Federico Onali, Renato Robledo, Laura Flore, Myosotis Massidda, Paolo Francalacci

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

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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

3 citing papers in PubMed, 4 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

6 authors at 1 institution in 1 country.

Carla M CalòDepartment of Life and Environment Sciences, University of Cagliari, Cagliari, Italy.
Federico OnaliDepartment of Life and Environment Sciences, University of Cagliari, Cagliari, Italy.
Renato RobledoDepartment of Biomedical Sciences, University of Cagliari, Cagliari, Italy.ORCID 0000-0003-0661-9309
Laura FloreDepartment of Life and Environment Sciences, University of Cagliari, Cagliari, Italy.
Myosotis MassiddaDepartment of Life and Environment Sciences, University of Cagliari, Cagliari, Italy.
Paolo FrancalacciDepartment of Life and Environment Sciences, University of Cagliari, Cagliari, Italy.
University of Cagliari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study is to analyze the worldwide distribution of SNP rs4870723 in COL14A1 gene to check if there are significant genetic differences among different populations and to test if the gene is a trait under selection.

methodsGenomic DNA was extracted from 69 unrelated individuals from Sardinia and genotyped for SNP rs4870723. Data were compared with 26 different populations, clustered in 5 super-populations, from the public 1000 genomes database. Allele frequency and heterozygosity were calculated with Genepop. The Hardy-Weinberg equilibrium and pairwise population differentiation through analysis of molecular variance (AMOVA FST) were determined with Arlequin.

resultsAllele frequencies of COL14A1 rs4870723 were compared in 27 populations clustered in 5 super-populations. All populations were in the Hardy-Weinberg equilibrium. In almost all populations, allele C was the most frequent allele, reaching the highest values in East Asia. The 27 populations showed an appreciable structure, with significant differences observed between European, African, and Asian populations.

conclusionSignificant differences were observed in the rs4870723 SNP distribution among the populations studied. However, we found no evidence for a selective pressure. Rather, the differentiation among the populations is likely the result of founder effect, genetic drift, and cultural factors, all events known to establish and maintain genetic diversity between populations.

Indexed as

Genetic DriftPolymorphism, Single NucleotideSelection, GeneticAfricaAsiaCollagenEuropeGene FrequencyGlycoproteinsHumansCOL14A1 protein, humanCollagenGlycoproteins1000 genomescollagenSardiniaselectionSNPs

Identifiers

PMID33650783
PMCPMC8123734
OpenAlexW3135841085

What OpenQuestion holds

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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.