Evidence map›Paper›PMID 42262907›Full record

ArticleJournal of animal science2026

Cytogenetic, genomic, and reproductive characterization of four Pura Raza Española Mares carrying a 64, X, del(X), t(X; Y) complex karyotype.

María Yuzhi Arjona-Delgado, Yamila Pirosanto, Terje Raudsepp, María Ángeles Vargas-Pérez, Mercedes Valera, Ana Encina, Pedro Azor, Monika Bugno-Poniewierska, Sebastián Demyda-Peyrás

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Article in Journal of animal science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

María Yuzhi Arjona-DelgadoDepartamento de Genética, Universidad de Córdoba, Campus de Rabanales, 14071, Córdoba, Spain.ORCID 0009-0007-4008-2871
Yamila PirosantoDepartamento de Producción Animal, Facultad de Ciencias Veterinarias, Universidad Nacional de La Plata, La Plata 1900, Argentina.
Terje RaudseppCollege of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, Texas 77843, United States.ORCID 0000-0003-2276-475X
María Ángeles Vargas-PérezDepartamento de Genética, Universidad de Córdoba, Campus de Rabanales, 14071, Córdoba, Spain.
Mercedes ValeraDepartamento de Agronomía, Escuela Técnica Superior de Ingeniería Agronómica, Universidad de Sevilla, Sevilla 41013, Spain.
Ana EncinaReal Asociación Nacional de Criadores de Caballos de Pura Raza Española (ANCCE), Sevilla 41012, Spain.
Pedro AzorReal Asociación Nacional de Criadores de Caballos de Pura Raza Española (ANCCE), Sevilla 41012, Spain.
Monika Bugno-PoniewierskaDepartment of Animal Reproduction, Anatomy and Genomics, University of Agriculture in Krakow, Kraków 31-120, Poland.
Sebastián Demyda-PeyrásDepartamento de Genética, Universidad de Córdoba, Campus de Rabanales, 14071, Córdoba, Spain.

Funding

María Yuzhi Arjona Delgado CNS2024-154334
6 · The paper itself

Abstract

Chromosomal abnormalities involving the sex chromosomes constitute critical genetic factors influencing fertility in horses. Nevertheless, a substantial proportion of individuals carrying sex chromosomal abnormalities exhibit normal reproductive phenotypes, which complicates their identification until adulthood. Here, we present four mares carrying a complex deletion/translocation rearrangement with the karyotype formula 64, X, del(X)(p∼25), t(X; Y)(p∼25; q∼15). The cases analyzed belong to three unrelated families of Pura Raza Española (PRE), all presenting the same chromosomal abnormality. Two of the individuals analyzed were a fertile mare and her foal, demonstrating vertical transmission of the rearrangement to the next generation. The animals were initially flagged for sex chromosome abnormalities due to incompatibilities between phenotypic and genotypic sex detected during STR analysis for parentage. They were subsequently analyzed for copy number abnormalities and sex chromosome assessment using an equine commercial SNP-array-based methodology, detecting a large heterozygous 10 Mb deletion located at the distal part of the ChrX p-arm, as well as the existence of a genomic region associated with ChrY. Fluorescence in situ hybridization (FISH) further confirmed that ChrY-derived material was translocated to the same distal part of the ChrX p-arm. Finally, bioinformatic tools were used to evaluate the abundance of CpG islands and to perform a functional analysis of the genes located in the affected regions. These results may suggest that reproductive competence in the fertile mare could be explained by the production of euploid zygotes carrying at least one copy of the intact X chromosome. This study highlights the importance of accurate detection and characterization of chromosomal abnormalities in horses, particularly in individuals with apparently normal reproductive phenotypes.

Indexed as

Horse DiseasesKaryotypeReproductionSex Chromosome AberrationsAnimalsFemaleHorsesKaryotypingequine cytogeneticsFISHgenomic screeningsex chromosomal abnormalitiesSNP arrayX-Y translocation

Identifiers

PMID42262907
PMCPMC13287993

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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.