Evidence map›Paper›PMID 37414574›Full record

ArticleGenome research2023

Large-scale detection and characterization of interchromosomal rearrangements in normozoospermic bulls using massive genotype and phenotype data sets.

Jeanlin Jourdain, Harmonie Barasc, Thomas Faraut, Anne Calgaro, Nathalie Bonnet, Camille Marcuzzo, Amandine Suin, Anne Barbat, Chris Hozé, Florian Besnard and 8 more

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Genome research, 2023. 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
–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

9 citing papers in PubMed, 19 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

18 authors at 4 institutions in 1 country.

Jeanlin JourdainEliance, 75012 Paris, France; jeanlin.jourdain@inrae.fr aurelien.capitan@inrae.fr.ORCID 0000-0002-5245-7382
Harmonie BarascGenPhySE, Université de Toulouse, INRAE, ENVT, 31320 Castanet-Tolosan, France.ORCID 0000-0002-1644-4701
Thomas FarautGenPhySE, Université de Toulouse, INRAE, ENVT, 31320 Castanet-Tolosan, France.ORCID 0000-0001-5156-3434
Anne CalgaroGenPhySE, Université de Toulouse, INRAE, ENVT, 31320 Castanet-Tolosan, France.
Nathalie BonnetGenPhySE, Université de Toulouse, INRAE, ENVT, 31320 Castanet-Tolosan, France.
Camille MarcuzzoINRAE, US 1426, GeT-PlaGe, Genotoul, France Génomique, Université Fédérale de Toulouse, 31320 Castanet-Tolosan, France.
Amandine SuinINRAE, US 1426, GeT-PlaGe, Genotoul, France Génomique, Université Fédérale de Toulouse, 31320 Castanet-Tolosan, France.
Anne BarbatUniversité Paris-Saclay, INRAE, AgroParisTech, GABI, G2B, 78350 Jouy-en-Josas, France.
Chris HozéEliance, 75012 Paris, France.ORCID 0000-0002-5900-5506
Florian BesnardUniversité Paris-Saclay, INRAE, AgroParisTech, GABI, G2B, 78350 Jouy-en-Josas, France.ORCID 0000-0002-1187-9132
Sébastien TaussatEliance, 75012 Paris, France.ORCID 0000-0002-3101-9471
Cécile GrohsUniversité Paris-Saclay, INRAE, AgroParisTech, GABI, G2B, 78350 Jouy-en-Josas, France.ORCID 0000-0002-3563-8966
Claire KuchlyINRAE, US 1426, GeT-PlaGe, Genotoul, France Génomique, Université Fédérale de Toulouse, 31320 Castanet-Tolosan, France.ORCID 0000-0001-8994-550X
Carole IampietroINRAE, US 1426, GeT-PlaGe, Genotoul, France Génomique, Université Fédérale de Toulouse, 31320 Castanet-Tolosan, France.ORCID 0000-0002-8148-4785
Cécile DonnadieuINRAE, US 1426, GeT-PlaGe, Genotoul, France Génomique, Université Fédérale de Toulouse, 31320 Castanet-Tolosan, France.ORCID 0000-0002-5164-3095
Alain PintonGenPhySE, Université de Toulouse, INRAE, ENVT, 31320 Castanet-Tolosan, France.ORCID 0000-0002-0809-7180
Didier BoichardUniversité Paris-Saclay, INRAE, AgroParisTech, GABI, G2B, 78350 Jouy-en-Josas, France.ORCID 0000-0003-0361-2961
Aurélien CapitanEliance, 75012 Paris, France; jeanlin.jourdain@inrae.fr aurelien.capitan@inrae.fr.ORCID 0000-0003-3185-0932
AgroParisTech · FRÉcole Nationale Vétérinaire de Toulouse · FRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRSupélec · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this paper, we developed a highly sensitive approach to detect interchromosomal rearrangements in cattle by searching for abnormal linkage disequilibrium patterns between markers located on different chromosomes in large paternal half-sib families genotyped as part of routine genomic evaluations. We screened 5571 families of artificial insemination sires from 15 breeds and revealed 13 putative interchromosomal rearrangements, 12 of which were validated by cytogenetic analysis and long-read sequencing. These consisted of one Robertsonian fusion, 10 reciprocal translocations, and the first case of insertional translocation reported in cattle. Taking advantage of the wealth of data available in cattle, we performed a series of complementary analyses to define the exact nature of these rearrangements, investigate their origins, and search for factors that may have favored their occurrence. We also evaluated the risks to the livestock industry and showed significant negative effects on several traits in the sires and in their balanced or aneuploid progeny compared with wild-type controls. Thus, we present the most comprehensive and thorough screen for interchromosomal rearrangements compatible with normal spermatogenesis in livestock species. This approach is readily applicable to any population that benefits from large genotype data sets, and will have direct applications in animal breeding. Finally, it also offers interesting prospects for basic research by allowing the detection of smaller and rarer types of chromosomal rearrangements than GTG banding, which are interesting models for studying gene regulation and the organization of genome structure.

Indexed as

GenomeTranslocation, GeneticAnimalsCattleGenomicsGenotypeMalePhenotype

Identifiers

PMID37414574
PMCPMC10519396
OpenAlexW4383313541

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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.