Evidence map›Paper›PMID 30987584›Full record

ArticleGenetics, selection, evolution : GSE2019

Two new structural mutations in the 5' region of the ASIP gene cause diluted feather color phenotypes in Japanese quail.

Annie Robic, Mireille Morisson, Sophie Leroux, David Gourichon, Alain Vignal, Noémie Thebault, Valérie Fillon, Francis Minvielle, Bertrand Bed'Hom, Tatiana Zerjal and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.1field-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

9 citing papers in PubMed, 38 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

11 authors at 3 institutions in 1 country.

Annie RobicGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France. annie.robic@inra.fr.ORCID http://orcid.org/0000-0003-3071-8614
Mireille MorissonGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
Sophie LerouxGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
David GourichonINRA PEAT, 37380, Tours, France.
Alain VignalGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
Noémie ThebaultGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
Valérie FillonGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
Francis MinvielleGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
Bertrand Bed'HomGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
Tatiana ZerjalGABI, INRA, AgroParisTech, Université Paris-Saclay, 78350, Jouy-en-Josas, France.
Frédérique PitelGenPhySE, Université de Toulouse, INRA, ENVT, 31326, Castanet-Tolosan, France.
École Nationale Vétérinaire de Toulouse · FRAgroParisTech · FRUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn quail, two feather colour phenotypes i.e. fawn-2/beige and yellow are associated with the ASIP locus. The aim of our study was to characterize the structural modifications within this locus that explain the yellow mutation (large deletion) and the fawn-2/beige mutation (assumed to be caused by a different structural modification).

resultsFor the yellow phenotype, we identified a complex mutation that involves a 141,162-bp long deletion. For the fawn-2/beige phenotype, we identified a 71-kb tandem duplication that comprises one unchanged copy of ASIP and one copy present in the ITCH-ASIP fusion gene, which leads to a transcript coding for a normal ASIP protein. Although this agrees with previous reports that reported an increased level of ASIP transcripts in the skin of mutant animals, we show that in the skin from fawn-2/beige embryos, this level is higher than expected with a simple duplication of the ASIP gene. Thus, we hypothesize that the 5' region of the ITCH-ASIP fusion gene leads to a higher transcription level than the 5' region of the ASIP gene.

conclusionsWe were able to conclude that the fawn-2 and beige phenotypes are caused by the same allele at the ASIP locus. Both of the associated mutations fawn-2/beige and yellow lead to the formation of a fusion gene, which encodes a transcript for the ASIP protein. In both cases, transcription of ASIP depends on the promoter of a different gene, which includes alternative up-regulating sequences. However, we cannot exclude the possibility that the loss of the 5' region of the ASIP gene itself has additional impacts, especially for the fawn-2/beige mutation. In addition, in several other species including mammals, the existence of other dominant gain-of-function structural modifications that are localized upstream of the ASIP coding sequences has been reported, which supports our hypothesis that repressors in the 5' region of ASIP are absent in the fawn-2/beige mutant.

Indexed as

Agouti Signaling ProteinAllelesAnimalsColorExonsFeathersGenotypeMutationPhenotypePigmentationQuailUntranslated RegionsAgouti Signaling ProteinUntranslated Regions

Identifiers

PMID30987584
PMCPMC6466734
OpenAlexW2945535846

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.