Detection of 30 bp DNA fragments with a sensitive modified Southern blot analysis

Author:

Takabatake Reona1,Kaneko Machiko1,Yanagida Makiko1,Kitta Kazumi1

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

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3