通过寡核苷酸介导的诱变进行基因修饰。转基因生物监管挑战?

Environmental biosafety research Pub Date : 2009-04-01 Epub Date: 2009-10-16 DOI:10.1051/ebr/2009007
Didier Breyer, Philippe Herman, Annick Brandenburger, Godelieve Gheysen, Erik Remaut, Patrice Soumillion, Jan Van Doorsselaere, René Custers, Katia Pauwels, Myriam Sneyers, Dirk Reheul
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引用次数: 49

摘要

在欧盟,转基因生物的定义是基于技术的。这意味着,一种新的生物只有在使用明确的技术开发出来的情况下,才会受到转基因生物监管框架的监管。这种方法现在受到新技术出现的挑战。在本文中,我们描述了与使用寡核苷酸介导的诱变开发新生物相关的监管和安全问题。我们提出科学论据,认为通过这种技术开发的生物不属于欧盟转基因生物法规的范围。我们的结论是,在这个问题上的任何政治决定都应该在欧盟层面广泛反思的基础上做出,同时避免在国际层面上出现分歧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic modification through oligonucleotide-mediated mutagenesis. A GMO regulatory challenge?

In the European Union, the definition of a GMO is technology-based. This means that a novel organism will be regulated under the GMO regulatory framework only if it has been developed with the use of defined techniques. This approach is now challenged with the emergence of new techniques. In this paper, we describe regulatory and safety issues associated with the use of oligonucleotide-mediated mutagenesis to develop novel organisms. We present scientific arguments for not having organisms developed through this technique fall within the scope of the EU regulation on GMOs. We conclude that any political decision on this issue should be taken on the basis of a broad reflection at EU level, while avoiding discrepancies at international level.

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