Suppr超能文献

利用源自鸟类CR1元件序列的PCR引物对DNA多态性进行定位。

Mapping DNA polymorphisms using PCR primers derived from the sequence of an avian CR1 element.

作者信息

Levin I, Crittenden L B, Dodgson J B

机构信息

Department of Microbiology, Michigan State University, East Lansing 48824.

出版信息

J Hered. 1994 Mar-Apr;85(2):73-8. doi: 10.1093/oxfordjournals.jhered.a111426.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验