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Rapid PCR-based determination of transgene copy number in rice
Authors:Fengling?Li,Moul?Dey,Chengkun?He,Vinod?Sangwan,Xianzhong?Wu,Ray?Wu  author-information"  >  author-information__contact u-icon-before"  >  mailto:ray.wu@cornell.edu"   title="  ray.wu@cornell.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Present address: Department of Molecular Biology & Genetics, Cornell University, 316 Biotechnology Building, 14853 Ithaca, NY, USA
Abstract:We present a simple, rapid, and low-cost method to determine transgene copy number in rice. More than 100 first- and second-generation transgenic rice plants were tested. The plasmid (pRCopy) used for rice transformation contains the specific gene of interest and a partially deleted cytochrome c gene (cyc), a single-copy gene in rice. A 132-bp segment of the cloned ricecyc was shortened to 108 bp by deleting a 24-bp internal fragment. After PCR amplification of the genomic DNA from transgenic rice harboring pRCopy, the 2 expected bands were found. The 121-bp band corresponds to the endogenouscyc; the 97-bp band comes from the integrated pRCopy. Clear distinctions can be made between single and multiple copies of the transgene by comparing band densities.
Keywords:rapid PCR method  transgene copy number
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