Benkel B F, Perreault J, Gagnon C, Conklin K
Agriculture and AgriFood Canada, Centre for Food and Animal Research, Ottawa, Ontario.
Anim Genet. 1995 Jun;26(3):189-91. doi: 10.1111/j.1365-2052.1995.tb03161.x.
A short fragment of chicken genomic DNA encompassing the insertion site of the endogenous avian leucosis viral element ev3 was isolated using the inverse polymerase chain reaction (inverse PCR) technique. The nucleotide sequence of the unoccupied site was used to design PCR primers that can be used to unambiguously determine the genetic status of any chicken, with respect to ev3. Screening of a small number of individuals from exotic breeds of chickens suggested that the frequency of ev3 is highly variable. The ev3 integration site shows a high degree of sequence homology with the macrophage-specific tyrosine kinase gene, bmk, in mice.
利用反向聚合酶链反应(Inverse PCR)技术分离出一段包含内源性禽白血病病毒元件ev3插入位点的鸡基因组DNA短片段。利用未被占据位点的核苷酸序列设计PCR引物,可用于明确确定任何鸡相对于ev3的遗传状态。对少数外来品种鸡个体的筛选表明,ev3的频率高度可变。ev3整合位点与小鼠巨噬细胞特异性酪氨酸激酶基因bmk具有高度的序列同源性。