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ACTN3 gene variants as potential phenotype and performance biomarkers in Brazilian sport horses training for eventing in a tropical climate.


ABSTRACT: The aim of this study was to look for mutations in the equine ACTN3 gene and to identify sequence variants that might be associated with the phenotype and performance of Brazilian sport horses training for events in a tropical climate. Among 17 such horses direct DNA sequencing and mutation analysis of the exon 15 and the intron-exon boundaries of ACTN3 revealed 2 new sequence variants in the ACTN3 intron 14-15, designated c.1681-86G > A and c.1681-129delA. Wild-type/deletion heterozygotes (A/del) had a lower mean subcutaneous fat layer in the region of the gluteus medius, as measured by ultrasonography, than the del/del homozygotes; the correlation was significant (P = 0.017). This single base-pair deletion in ACTN3 intron 14-15 may have resulted in metabolic changes that led to increased deposition of body fat in the homozygous state. However, neither sequence variant was correlated with the time to fatigue in a test on a high-speed treadmill with an incremental-speed protocol.

SUBMITTER: Padilha FGF 

PROVIDER: S-EPMC6040019 | biostudies-other | 2018 Jul

REPOSITORIES: biostudies-other

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<i>ACTN3</i> gene variants as potential phenotype and performance biomarkers in Brazilian sport horses training for eventing in a tropical climate.

Padilha Felipe Gomes Ferreira FGF   El-Jaick Kênia Balbi KB   de Castro Liane L   Dos Santos Moreira Aline A   de Almeida Fernando Queiroz FQ   Ferreira Ana Maria Reis AMR  

Canadian journal of veterinary research = Revue canadienne de recherche veterinaire 20180701 3


The aim of this study was to look for mutations in the equine <i>ACTN3</i> gene and to identify sequence variants that might be associated with the phenotype and performance of Brazilian sport horses training for events in a tropical climate. Among 17 such horses direct DNA sequencing and mutation analysis of the exon 15 and the intron-exon boundaries of <i>ACTN3</i> revealed 2 new sequence variants in the <i>ACTN3</i> intron 14-15, designated c.1681-86G > A and c.1681-129delA. Wild-type/deletio  ...[more]

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