Levin I, Crittenden L B, Dodgson J B
Department of Microbiology, Michigan State University, East Lansing 48824.
J Hered. 1994 Mar-Apr;85(2):73-8. doi: 10.1093/oxfordjournals.jhered.a111426.
Primers complementary to the chicken middle repetitive sequence element CR1 were used to generate and simultaneously map polymorphic polymerase chain reaction products (CR1-PCR) with various chicken DNAs as templates. Ten primers were prepared using the sequence of a single CR1 element as a guide. These 10 primers generated 23 polymorphic CR1-PCR products. The average number of polymorphic CR1-PCR products generated using single primers (1.1 per primer) was significantly higher than the average number observed using combinations of two primers (0.3 per primer combination). The polymorphic CR1-PCR products were mapped in a subset of a reference backcross population designed for the genetic linkage analysis of the chicken. Nineteen of the polymorphic CR1-PCR products identified were assigned to 13 of 19 linkage groups characterized thus far in this population; three have yet to be linked to a specific map location. One of the CR1-PCR markers mapped to the chicken Z chromosome. There was no evidence for a significant clustering of CR1-PCR markers within the map, even at the site of the CR1 element whose sequence was used for primer design.
使用与鸡的中间重复序列元件CR1互补的引物,以各种鸡DNA为模板生成并同时定位多态性聚合酶链反应产物(CR1-PCR)。以单个CR1元件的序列为指导制备了10种引物。这10种引物产生了23种多态性CR1-PCR产物。使用单个引物产生的多态性CR1-PCR产物的平均数(每个引物1.1个)显著高于使用两个引物组合观察到的平均数(每个引物组合0.3个)。将多态性CR1-PCR产物定位在为鸡的遗传连锁分析设计的参考回交群体的一个子集中。鉴定出的19种多态性CR1-PCR产物被分配到该群体中迄今已鉴定的19个连锁群中的13个;有3个尚未与特定的图谱位置连锁。其中一个CR1-PCR标记定位到鸡的Z染色体上。即使在用于引物设计的CR1元件的位点,也没有证据表明CR1-PCR标记在图谱内有明显的聚集。