Yi Cheng Xin, Zhang Jun, Chan Ka Man, Liu Xiao Kun, Hong Yan
Temasek Life Sciences Laboratory, National University of Singapore, Singapore 117604, Singapore.
Anal Biochem. 2008 Apr 1;375(1):150-2. doi: 10.1016/j.ab.2007.11.022. Epub 2007 Nov 22.
A TaqMan quantitative real-time PCR detection system was developed to examine transgene copy number in cotton. GhUBC1, a gene validated to be present as a single copy per haploid Gossypium hirsutum genome, was used as the endogenous reference to estimate copy number of GFP and selection marker NPTII in 28 T0 plants. This system was found to be more accurate than genomic Southern blot hybridization and could effectively tell homozygotes from heterozygotes in a T1 transgenic cotton population. Therefore it is suitable for efficient and cost effective early screening of transgenic seedlings and identifying transgene homozygotes in segregation populations.
开发了一种TaqMan定量实时PCR检测系统,用于检测棉花中的转基因拷贝数。GhUBC1基因经证实,在单倍体陆地棉基因组中以单拷贝形式存在,被用作内参,以估计28株T0代植株中绿色荧光蛋白(GFP)和选择标记新霉素磷酸转移酶II(NPTII)的拷贝数。该系统比基因组Southern杂交更准确,并且能够有效区分T1代转基因棉花群体中的纯合子和杂合子。因此,它适用于高效且经济高效地早期筛选转基因幼苗,并在分离群体中鉴定转基因纯合子。