Evidence map›Paper›PMID 37758900›Full record

ArticleHeredity2023

Fine mapping of the Cepaea nemoralis shell colour and mid-banded loci using a high-density linkage map.

Margrethe Johansen, Suzanne Saenko, Menno Schilthuizen, Wellcome Sanger Institute Tree of Life Programme, Mark Blaxter, Angus Davison

Abstract read
In one paragraph

Article in Heredity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Margrethe JohansenSchool of Life Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, UK. m-johansen@outlook.com.ORCID 0000-0003-1321-8546
Suzanne SaenkoEvolutionary Ecology, Naturalis Biodiversity Center, Leiden, 2333CR, The Netherlands.
Menno SchilthuizenEvolutionary Ecology, Naturalis Biodiversity Center, Leiden, 2333CR, The Netherlands.ORCID 0000-0001-6229-0347
Wellcome Sanger Institute Tree of Life Programme
Mark BlaxterWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.ORCID 0000-0003-2861-949X
Angus DavisonSchool of Life Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, UK.ORCID 0000-0003-2554-8585

Funding

Wellcome TrustWellcome Trust 206194
6 · The paper itself

Abstract

Molluscs are a highly speciose phylum that exhibits an astonishing array of colours and patterns, yet relatively little progress has been made in identifying the underlying genes that determine phenotypic variation. One prominent example is the land snail Cepaea nemoralis for which classical genetic studies have shown that around nine loci, several physically linked and inherited together as a 'supergene', control the shell colour and banding polymorphism. As a first step towards identifying the genes involved, we used whole-genome resequencing of individuals from a laboratory cross to construct a high-density linkage map, and then trait mapping to identify 95% confidence intervals for the chromosomal region that contains the supergene, specifically the colour locus (C), and the unlinked mid-banded locus (U). The linkage map is made up of 215,593 markers, ordered into 22 linkage groups, with one large group making up ~27% of the genome. The C locus was mapped to a ~1.3 cM region on linkage group 11, and the U locus was mapped to a ~0.7 cM region on linkage group 15. The linkage map will serve as an important resource for further evolutionary and population genomic studies of C. nemoralis and related species, as well as the identification of candidate genes within the supergene and for the mid-banding phenotype.

Indexed as

GenomePolymorphism, GeneticChromosome MappingColorGenetic LinkageHumansPhenotype

Identifiers

PMID37758900
PMCPMC10673960

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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.