A unique characteristic of the Silkie chicken is its fibromelanosis phenotype.The dermal layer of its skin,its connective tissue and shank dermis are hyperpigmented.This dermal hyperpigmentation phenotype is controlle...A unique characteristic of the Silkie chicken is its fibromelanosis phenotype.The dermal layer of its skin,its connective tissue and shank dermis are hyperpigmented.This dermal hyperpigmentation phenotype is controlled by the sex-linked inhibitor of dermal melanin gene(ID)and the dominant fibromelanosis allele.This study attempted to confirm the genomic region associated with ID.By genotyping,ID was found to be closely linked to the region between GGA_rs16127903 and GGA_rs14685542(8406919 bp)on chromosome Z,which contains ten functional genes.The expression of these genes was characterized in the embryo and 4 days after hatching and it was concluded that MTAP,encoding methylthioadenosinephosphorylase,would be the most likely candidate gene.Finally,target DNA capture and sequence analysis was performed,but no specific SNP(s)was found in the targeted region of the Silkie genome.Further work is necessary to identify the causal ID mutation located on chromosome Z.展开更多
基金This work was funded by the National Natural Science Foundation of China(U0831003)the National Advanced Technology Research and Development Program of China(2011AA100301).
文摘A unique characteristic of the Silkie chicken is its fibromelanosis phenotype.The dermal layer of its skin,its connective tissue and shank dermis are hyperpigmented.This dermal hyperpigmentation phenotype is controlled by the sex-linked inhibitor of dermal melanin gene(ID)and the dominant fibromelanosis allele.This study attempted to confirm the genomic region associated with ID.By genotyping,ID was found to be closely linked to the region between GGA_rs16127903 and GGA_rs14685542(8406919 bp)on chromosome Z,which contains ten functional genes.The expression of these genes was characterized in the embryo and 4 days after hatching and it was concluded that MTAP,encoding methylthioadenosinephosphorylase,would be the most likely candidate gene.Finally,target DNA capture and sequence analysis was performed,but no specific SNP(s)was found in the targeted region of the Silkie genome.Further work is necessary to identify the causal ID mutation located on chromosome Z.
