Discovering of genomic variations associated to growth traits by gwas in braunvieh cattle

José Luis Zepeda-Batista, Rafael Núñez-Domínguez, Rodolfo Ramírez-Valverde, Francisco Joel Jahuey-Martínez, Jessica Beatriz Herrera-Ojeda, Gaspar Manuel Parra-Bracamonte

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

A genome-wide association study (GWAS) was performed to elucidate genetic architecture of growth traits in Braunvieh cattle. Methods: The study included 300 genotyped animals by the GeneSeek® Genomic Profiler Bovine LDv.4 panel; after quality control, 22,734 SNP and 276 animals were maintained in the analysis. The examined phenotypic data considered birth (BW), weaning (WW), and yearling weights. The association analysis was performed using the principal components method via the egscore function of the GenABEL version 1.8-0 package in the R environment. The marker rs133262280 located in BTA 22 was associated with BW, and two SNPs were associated with WW, rs43668789 (BTA 11) and rs136155567 (BTA 27). New QTL associated with these liveweight traits and four positional and functional candidate genes potentially involved in variations of the analyzed traits were identified. The most important genes in these genomic regions were MCM2 (minichromosome maintenance complex component 2), TPRA1 (transmembrane protein adipocyte associated 1), GALM (galactose mutarotase), and NRG1 (neuregulin 1), related to embryonic cleavage, bone and tissue growth, cell adhesion, and organic development. This study is the first to present a GWAS conducted in Braunvieh cattle in Mexico providing evidence for genetic architecture of assessed growth traits. Further specific analysis of found associated genes and regions will clarify its contribution to the genetic basis of growth-related traits.

Original languageEnglish
Article number1666
JournalGenes
Volume12
Issue number11
DOIs
StatePublished - Nov 2021

Keywords

  • Association
  • Candidate gene
  • Growth
  • Quantitative trait loci
  • Single nucleotide polymorphism

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