African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12487

Full Length Research Paper

Determination of genotype differences through restriction endonuclease in Camels (Camelus dromedarius)

Muhammad  Ghias  Uddin  Shah1,  Monika  Reissmann2,  Anas  Sarwar  Qureshi3,  Horst  Jurgen Schwartz4,  Muhammad  Shuaib  Khan5*,Tariq Ali 6  Ali  Zaman5,    Kamran  Safdar5 , Khalid  Muhammad5 and Shakeeb  Ullah5      
1Department of Anatomy and Histology, Sindh Agriculture University, TandoJam, Pakistan. 2Institute of Animal Sciences, Humboldt-Universität zu Berlin, Germany. 3Department of Veterinary Anatomy, University of Agriculture Faisalabad, Pakistan. 4Department of Livestock Ecology, Humboldt-Universität zu Berlin, Germany. 5Gomal College of Veterinary Sciences, Gomal University D I Khan, Pakistan. 6livestock Research and development station Paharpur D.I. Khan  
Email: [email protected]

  •  Accepted: 08 June 2012
  •  Published: 31 July 2012

Abstract

Tyrosinase gene or C locus has long been implicated in the coat colour determination.This gene a copper-containing enzyme located on chromosome 11q14.3 is expressed in melanocytes and controls the major steps in pigment production. In camel, C locus a restriction site provoked by the T variant of the mutation was used in a special restriction fragment length polymorphism analysis (PCR-RFLP) for genotyping of camels from six different Pakistani camel breeds (Marecha, Dhatti, Larri, Kohi, Campbelpuri and Sakrai). Significant differences in the genotype frequency between the breeds were estimated. The Sakrai breed showed in comparison to other studied breeds a distinctly higher frequency of the homozygous with restriction genotype. The objective of the present study was to screen the camel breeds using modern genetic technique that have been so far classified on the basis of performance and tribal ownership.

 

Key words: Camel, genotype, restriction endonuclease.