Evidence map›Paper›PMID 38424485›Full record

ArticleGenetics, selection, evolution : GSE2024

Searching for homozygous haplotype deficiency in Manech Tête Rousse dairy sheep revealed a nonsense variant in the MMUT gene affecting newborn lamb viability.

Maxime Ben Braiek, Carole Moreno-Romieux, Céline André, Jean-Michel Astruc, Philippe Bardou, Arnaud Bordes, Frédéric Debat, Francis Fidelle, Itsasne Granado-Tajada, Chris Hozé and 6 more

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

16 authors at 5 institutions in 2 countries.

Maxime Ben BraiekGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.ORCID http://orcid.org/0000-0003-4770-0867
Carole Moreno-RomieuxGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Céline AndréCDEO, Quartier Ahetzia, 64130, Ordiarp, France.
Jean-Michel AstrucInstitut de l'Elevage, 24 Chemin de Borde-Rouge, 31321, Castanet-Tolosan, France.
Philippe BardouINRAE, 31326, Castanet-Tolosan, France.
Arnaud BordesGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Frédéric DebatGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Francis FidelleCDEO, Quartier Ahetzia, 64130, Ordiarp, France.
Itsasne Granado-TajadaDepartment of Animal Production, NEIKER-BRTA Basque Institute of Agricultural Research and Development, Agrifood Campus of Arkaute s/n, 01080, Arkaute, Spain.ORCID http://orcid.org/0000-0002-6557-1467
Chris HozéEliance, 149 Rue de Bercy, 75595, Paris, France.
Florence Plisson-PetitGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
François RivemaleGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Julien SarryGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Némuel TadiGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Florent WoloszynGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France.
Stéphane FabreGenPhySE, Université de Toulouse, INRAE, ENVT, 31326, Castanet-Tolosan, France. stephane.fabre@inrae.fr.ORCID http://orcid.org/0000-0001-7350-9500
École Nationale Vétérinaire de Toulouse · FRInstitut de l’Elevage · FRAgroParisTech · FRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRNEIKER, the Basque Institute for Agricultural Research and Development · ES

Funding

APIS-GENE HOMLETHorizon 2020 772787 SMARTERMinistère de l'Agriculture et de l'Alimentation CASDAR n°20ART1532777Région Occitanie Pyrénées-Méditerranée HOMLET
6 · The paper itself

Abstract

backgroundRecessive deleterious variants are known to segregate in livestock populations, as in humans, and some may be lethal in the homozygous state.

resultsWe used phased 50 k single nucleotide polymorphism (SNP) genotypes and pedigree data to scan the genome of 6845 Manech Tête Rousse dairy sheep to search for deficiency in homozygous haplotypes (DHH). Five Manech Tête Rousse deficient homozygous haplotypes (MTRDHH1 to 5) were identified, with a homozygous deficiency ranging from 84 to 100%. These haplotypes are located on Ovis aries chromosome (OAR)1 (MTRDHH2 and 3), OAR10 (MTRDHH4), OAR13 (MTRDHH5), and OAR20 (MTRDHH1), and have carrier frequencies ranging from 7.8 to 16.6%. When comparing at-risk matings between DHH carriers to safe matings between non-carriers, two DHH (MTRDHH1 and 2) were linked with decreased insemination success and/or increased stillbirth incidence. We investigated the MTRDHH1 haplotype, which substantially increased stillbirth rate, and identified a single nucleotide variant (SNV) inducing a premature stop codon (p.Gln409*) in the methylmalonyl-CoA mutase (MMUT) gene by using a whole-genome sequencing approach. We generated homozygous lambs for the MMUT mutation by at-risk mating between heterozygous carriers, and most of them died within the first 24 h after birth without any obvious clinical symptoms. Reverse transcriptase-qPCR and western blotting on post-mortem liver and kidney biological samples showed a decreased expression of MMUT mRNA in the liver and absence of a full-length MMUT protein in the mutant homozygous lambs.

conclusionsWe identified five homozygous deficient haplotypes that are likely to harbor five independent deleterious recessive variants in sheep. One of these was detected in the MMUT gene, which is associated with lamb lethality in the homozygous state. A specific management of these haplotypes/variants in the MTR dairy sheep selection program would help enhance the overall fertility and lamb survival.

Indexed as

StillbirthAnimalsAnimals, NewbornFemaleGenotypeHaplotypesHomozygoteHumansPregnancySheep

Identifiers

PMID38424485
PMCPMC10905913
OpenAlexW4392298311

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.