Affiliation:
1. Division of Analytical Science, Food Research Institute, National Agriculture and Food Research Organization, Tsukuba, Japan
Abstract
Abstract
To evaluate crops generated by new breeding techniques, it is important to confirm the removal of recombinant DNAs (rDNAs) derived from foreign genes including unintentionally introduced short rDNA(s). We attempted to develop a sensitive detection method for such short rDNAs using Southern blot analysis and performed a model study targeting single-copy endogenous genes in plants. To increase the detection sensitivity, the general protocol for Southern blot analysis was modified. In the model study, we used endogenous-gene-targeting probes in which complementary sequences were serially replaced by dummy sequences, and detected complementary sequences as well as 30 bp. We further evaluated the sensitivity using short rDNAs derived from GM sequences as pseudoinsertions, and the results demonstrated that rDNA-insertions as small as 30 bp could be detected. The results suggested that unintentionally introduced rDNA-insertions were 30 bp or more in length could be detected by the Southern blot analysis.
Funder
Cabinet Office, Government of Japan
SIP
Publisher
Oxford University Press (OUP)
Subject
Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology
Reference45 articles.
1. PCR technology for screening and quantification of genetically modified organisms (GMOs);Holst-Jensen;Anal Bioanal Chem,2003
2. Novel reference molecules for quantification of genetically modified maize and soybean;Kuribara;J AOAC Int,2002
3. Joint Research Centre
. [cited 2020 Apr08]. Available from: http://gmo-crl.jrc.ec.europa.eu/StatusOfDossiers.aspx.
4. Notification 201 of November 16
. (2012). Consumer affairs agency, government of Japan.
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献