Marcadores snp asociados a terneza en dos músculos, Flexor Digitorum y Psoas Major, en avileña negra ibérica

• Ximena Quintero Arboleda ^[2] ; MªJesús Carabaño ^[2] ; Guillherme Venturini ^[3] ; Cristina Meneses ^[2] ; Julia Rueda ^[1] ; Clara Díaz ^[2]
  1. [1] Universidad Complutense de Madrid

     Universidad Complutense de Madrid

     Madrid, España

     
  2. [2] INIA
  3. [3] FCAV-UNESP-Jaboticabal

  Mostrar afiliaciones +
• Localización: XV Jornadas sobre Producción Animal: 14 y 15 de mayo de 2013, Zaragoza / Jorge Hugo Calvo Lacosta (aut.), Isabel Casasús Pueyo (aut.), Margalida Joy Torrens (aut.), Javier Álvarez Rodríguez (aut.), Luis Varona Aguado (aut.), Begoña Panea Doblado (aut.), Carlos Calvete Margolles (aut.), Joaquim Barcells Teres (aut.), Vol. 2, 2013, ISBN 978-84-695-7684-7, págs. 529-531
• Idioma: español
• Títulos paralelos:
  • Snps markers associated to tenderness in two different muscles Flexor Digitorum and Psoas Major, in avileña negra ibérica breed
• Enlaces
  • Texto Completo Libro  1 (pdf)   2 (pdf) 
• Resumen

  • This study aimed at identifying genetic markers associated with beef tenderness in two largely different muscles, Psoas major (PM) en Flexor digitorum (FD). A total of 397 Avileña-Negra Ibérica calves with genotypes for the Illumina Bovine SNP50 platform and measures of organoleptic tenderness (OT) and Warner-Blazter compression (WBC) participated in the study. A pre-selection of SNPs was carried out by determining the SNPs contained in 140 QTL regions previously identified as associated with beef tenderness in the Animal Genome UMD_3.1 database. A genome wide association study (GWAS) was then performed using QXpak 5.2. A model including place-year and length of fattening, age, place and season of slaughter, panel session and panelist (only for OT), one SNP at a time and the polygenic additive effect was used. A total of 4101 SNPs were pre-selected. The GWAS revealed that 3/0 and 5/0 SNPs were associated to OT and WBC in FD/PM for a 12 and a 7 % FDR threshold, respectively. The SNP of largest effect was responsible for a of 7% and 32% of the total additive genetic variance of OT and WBC inFD, respectively. These results suggest a differential pattern of genetic regulation of tenderness between the two muscles