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首页> 外文期刊>Food analytical methods >Next-generation sequencing as a tool for detailed molecular characterisation of genomic insertions and flanking regions in genetically modified plants: a pilot study using a rice event unauthorised in the EU.
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Next-generation sequencing as a tool for detailed molecular characterisation of genomic insertions and flanking regions in genetically modified plants: a pilot study using a rice event unauthorised in the EU.

机译:下一代测序可作为对转基因植物中的基因组插入和侧翼区域进行详细分子表征的工具:一项使用欧盟未经许可的水稻事件的试点研究。

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摘要

Precise molecular characterisation of genetic modifications integrated into the genomes of genetically modified organisms (GMOs) and of their flanking genomic regions forms a key component for the development of event-specific detection methods. In the EU, this information is of particular importance for risk management in cases where genetic modifications of unauthorised GM food, feed or seeds are detected. PCR-based chromosome walking approaches are commonly used for DNA sequence determination of the genetic modifications and of the flanking genomic regions in yet undescribed GM plants. If the plant contains complex and re-arranged modifications, sequencing and molecular characterisation are often difficult and laborious. Next-generation sequencing (NGS) of DNA is a powerful alternative tool to rapidly generate primary sequence data on the genome of so far uncharacterised sample material if pure GMO material is available. Recently, robust NGS platforms and affordable sequencing services are accessible for food and feed control laboratories. We here present a NGS-based study for whole-genome sequencing of the GM rice event LLRice62 as a proof-of-principle experiment to develop bioinformatics easy-to-use data analysis tools for rapid molecular characterisation. A total of 171,657,155 read mate pairs of approximately 75 bp each were obtained. Sequence reads belonging to the genetic modifications and their flanking genomic regions in LLRice62 were identified by bioinformatic comparison to the corresponding Oryza sativa ssp. japonica reference genome sequence using the Illumina InDel caller software and subsequent iterative mapping of retrieved NGS reads. An entire genetic modification of 1,493 bp in the genome of the LLRice62 sample material was determined and correctly mapped on chromosome 6. The determined nucleotide sequence coincides to the genetic modification described by the developer of this rice event. This study demonstrates for the first time the applicability of NGS for molecular characterisation of uncharacterised GMOs. copyright Springer Science+Business Media New York 2013.
机译:整合到转基因生物(GMO)及其侧翼基因组区域的基因组中的遗传修饰的精确分子表征是开发事件特异性检测方法的关键组成部分。在欧盟,如果检测到未经授权的转基因食品,饲料或种子的基因改造,则此信息对于风险管理尤为重要。基于PCR的染色体步移方法通常用于确定尚未描述的GM植物的遗传修饰和侧翼基因组区域的DNA序列。如果植物包含复杂且重新排列的修饰,则测序和分子表征通常会很困难且费力。 DNA的下一代测序(NGS)是一种功能强大的替代工具,如果可以使用纯GMO材料,则可以在迄今为止尚未鉴定的样品材料的基因组上快速生成一级序列数据。最近,食品和饲料控制实验室可以使用强大的NGS平台和负担得起的测序服务。我们在这里提出了一项基于NGS的转基因水稻事件LLRice62全基因组测序研究,作为一项原理证明实验,旨在开发生物信息学易于使用的数据分析工具,以进行快速分子表征。总共获得171,657,155个读伴侣对,每个对大约75 bp。通过与相应的稻(Oryza sativa ssp)的生物信息学比较,鉴定了属于LLRice62基因修饰及其侧翼基因组区域的序列读段。使用Illumina InDel调用者软件进行粳稻参考基因组序列分析,然后对检索到的NGS读数进行迭代映射。确定了LLRice62样品材料基因组中1,493 bp的完整遗传修饰,并正确定位在6号染色体上。确定的核苷酸序列与该水稻事件的开发者描述的遗传修饰相符。这项研究首次证明了NGS在未表征的GMO分子表征中的适用性。版权所有Springer Science + Business Media纽约,2013年。

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