Causative Gene Discovery for Sheep Inherited Disorders
نویسنده
چکیده
and Implications Chondrodysplasia, inherited rickets and lower motor neuron disease are three sheep disorders in New Zealand that have been recently shown to be inherited apparently in a recessive manner. To discover the causative genes involved in the above diseases, around 50,000 genetic differences called single nucleotide polymorphisms (SNPs) throughout the genome were tested to define homozygous regions, one of which should harbor the causative mutation. Fine mapping of these regions for each disease was performed by discovering new SNPs located on candidate genes in these regions. To date, responsible mutations were successfully identified for inherited rickets and lower motor neuron disease. Our findings will benefit sheep breeding practices by providing a tool that can be used to avoid atrisk mating and may benefit science by providing animal disease models for human studies.
منابع مشابه
Screening for Causative Mutations of Major Prolificacy Genes in Iranian Fat-Tailed Sheep
Objective The presence of different missense mutations in sheep breeds have shown that the bone morphogenetic protein receptor 1B (BMPR1B), bone morphogenetic protein 15 (BMP15) and growth differentiation factor 9 (GDF9) genes play a vital role in ovulation rate and prolificacy in ewes. Therefore, the present study investigates BMPR1B, BMP15 and GDF9 genes mutations in prolific ewes of Iranian ...
متن کاملMolecular diagnosis of Mycoplasma conjunctivae in an outbreak of infectious keratoconjunctivitis in sheep
Infectious keratoconjunctivitis (IKC) is a painful, highly contagious ocular disease in sheep and goats. This study was carried out for identification and characterization of causative agent of ocular disease in a sheep flock consisting of 300 ewes in Mashhad, Iran. Several ocular swabs were taken from affected animals. The samples were pooled and processed in a laboratory for isolation of susp...
متن کاملMicrophthalmia in Texel Sheep Is Associated with a Missense Mutation in the Paired-Like Homeodomain 3 (PITX3) Gene
Microphthalmia in sheep is an autosomal recessive inherited congenital anomaly found within the Texel breed. It is characterized by extremely small or absent eyes and affected lambs are absolutely blind. For the first time, we use a genome-wide ovine SNP array for positional cloning of a Mendelian trait in sheep. Genotyping 23 cases and 23 controls using Illumina's OvineSNP50 BeadChip allowed u...
متن کاملThe Polymorphism of FecXG Region Exon 2 of BMP15 Gene in Hisari Sheep
Booroola gene is one of the major genes in the enhancement of ovulation rate and could be an attractive candidate gene for ovulation rate in sheep. Molecular technologies have been widely used for discovery of mutations in animal species. These mutations have major effects on the important economic traits of sheep and goats. This study was conducted to identify the mutation in FecXG region of e...
متن کاملنگاهی به ژن درمانی، پیشرفتهای اخیر و چشم انداز آینده
Human gene therapy has attracted increasing attention as a highly encouraging therapeutic approach to treat wide variety of diseases, other than genetically inherited and monogenic disorders. This approach entails the introduction and expression of a variety of nucleic acids into human target cells for therapeutic purposes. In this article, we review the history, highlights, recently progresses...
متن کامل