Guo Qing-hua, Guo Mei-li
Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Yao Xue Xue Bao. 2007 Jul;42(7):794-7.
Sequence related amplified polymorphism (SRAP) technique was used to identify SRAP fragment linked to Carthamus tinctorius L. spines of outer involucral bract (OIB) , experimental evidence for molecular marker assistant breeding of Carthamus tinctorius L. has been provided. Based on the strategy of bulk segregate analysis (BSA), two gene pools were separately constructed according to the extreme trait of OIB with many long spines and no spines from Carthamus tinctorius L. Forty-five pairs of SRAP primers were selected and screened from two parents and two gene pools, and one SRAP marker M3E3 was found to be linked to the spines in segregating F2 population confirmation. M3E3 SRAP band was excised, cloned and sequenced. In 20 spininess individuals, this marker was present in 16 spininess individuals and absent in 4 individuals. This band was absent in the 15 spineless F, segregating individuals, which accounted for 11.4% recombination. The M3E3 extract length was 349bp, of which the base components of A + T accounted for 41. 08%. One SRAP marker M3E3 linked to the spines in Carthamus tinctorius L. will be of good use for breeding spineless cultivars at the molecular level in the future.
采用序列相关扩增多态性(SRAP)技术鉴定与红花外总苞片(OIB)刺相关的SRAP片段,为红花分子标记辅助育种提供了实验依据。基于集群分离分析法(BSA),根据红花OIB多长刺和无刺的极端性状分别构建两个基因池。从两个亲本和两个基因池中筛选出45对SRAP引物,在分离的F2群体验证中发现一个SRAP标记M3E3与刺相关。切下M3E3 SRAP条带,进行克隆和测序。在20个有刺个体中,该标记在16个有刺个体中存在,在4个个体中不存在。在15个无刺的F1分离个体中该条带不存在,重组率为11.4%。M3E3片段长度为349bp,其中A+T碱基组成占41.08%。一个与红花刺相关的SRAP标记M3E3将来在分子水平上对培育无刺品种有很好的用途。