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Identification of single nucleotide polymorphism in protein phosphatase 1 regulatory subunit 11 gene in Murrah bulls.
Jain, Varsha; Patel, Brijesh; Umar, Farhat Paul; Ajithakumar, H M; Gurjar, Suraj K; Gupta, I D; Verma, Archana.
Afiliación
  • Jain V; Division of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
  • Patel B; Livestock Production Management Section, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
  • Umar FP; Division of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
  • Ajithakumar HM; Division of Animal Physiology, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
  • Gurjar SK; Division of Animal Physiology, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
  • Gupta ID; Division of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
  • Verma A; Division of Animal Genetics and Breeding, ICAR-National Dairy Research Institute, Karnal, Haryana, India.
Vet World ; 10(2): 244-248, 2017 Feb.
Article en En | MEDLINE | ID: mdl-28344410
AIM: This study was conducted with the objective to identify single nucleotide polymorphism (SNP) in protein phosphatase 1 regulatory subunit 11 (PPP1R11) gene in Murrah bulls. MATERIALS AND METHODS: Genomic DNA was isolated by phenol-chloroform extraction method from the frozen semen samples of 65 Murrah bulls maintained at Artificial Breeding Research Centre, ICAR-National Dairy Research Institute, Karnal. The quality and concentration of DNA was checked by spectrophotometer reading and agarose gel electrophoresis. The target region of PPP1R11 gene was amplified using four sets of primer designed based on Bos taurus reference sequence. The amplified products were sequenced and aligned using Clustal Omega for identification of SNPs. Animals were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) using EcoNI restriction enzyme. RESULTS: The sequences in the NCBI accession number NW_005785016.1 for Bubalus bubalis were compared and aligned with the edited sequences of Murrah bulls with Clustal Omega software. A total of 10 SNPs were found, out of which 1 at 5'UTR, 3 at intron 1, and 6 at intron 2 region. PCR-RFLP using restriction enzyme EcoNI revealed only AA genotype indicating monomorphism in PPP1R11 gene of all Murrah animals included in the study. CONCLUSION: A total of 10 SNPs were found. PCR-RFLP revealed only AA genotype indicating monomorphism in PPP1R11 gene of all Murrah animals included in the study, due to which association analysis with conception rate was not feasible.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Vet World Año: 2017 Tipo del documento: Article País de afiliación: India Pais de publicación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Vet World Año: 2017 Tipo del documento: Article País de afiliación: India Pais de publicación: India