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在对用于快速循环育种的转基因苹果T1190进行全基因组测序后,未发现意外转基因插入的证据。

No Evidence of Unexpected Transgenic Insertions in T1190 - A Transgenic Apple Used in Rapid Cycle Breeding - Following Whole Genome Sequencing.

作者信息

Patocchi Andrea, Keilwagen Jens, Berner Thomas, Wenzel Stefanie, Broggini Giovanni A L, Altschmied Lothar, Hanke Magda-Viola, Flachowsky Henryk

机构信息

Research Division Plant Breeding, Agroscope, Wädenswil, Switzerland.

Julius Kühn-Institut (JKI), Federal Research Centre for Cultivated Plants, Institute for Biosafety in Plant Biotechnology, Quedlinburg, Germany.

出版信息

Front Plant Sci. 2021 Aug 11;12:715737. doi: 10.3389/fpls.2021.715737. eCollection 2021.

Abstract

Rapid cycle breeding uses transgenic early flowering plants as crossbreed parents to facilitate the shortening of breeding programs for perennial crops with long-lasting juvenility. Rapid cycle breeding in apple was established using the transgenic genotype T1190 expressing the gene of silver birch. In this study, the genomes of T1190 and its non-transgenic wild-type PinS (F1-offspring of 'Pinova' and 'Idared') were sequenced by Illumina short-read sequencing in two separate experiments resulting in a mean sequencing depth of 182× for T1190 and 167× for PinS. The sequencing revealed 8,450 reads, which contain sequences of ≥20 bp identical to the plant transformation vector. These reads were assembled into 125 contigs, which were examined to see whether they contained transgenic insertions or if they are not using a five-step procedure. The sequence of one contig represents the known T-DNA insertion on chromosome 4 of T1190. The sequences of the remaining contigs were either equally present in T1190 and PinS, their part with sequence identity to the vector was equally present in apple reference genomes, or they seem to result from endophytic contaminations rather than from additional transgenic insertions. Therefore, we conclude that the transgenic apple plant T1190 contains only one transgenic insertion, located on chromosome 4, and shows no further partial insertions of the transformation vector. Accession Numbers: JQ974028.1.

摘要

快速循环育种利用转基因早花植物作为杂交亲本,以促进缩短多年生作物漫长幼龄期的育种计划。苹果的快速循环育种是利用表达白桦基因的转基因基因型T1190建立的。在本研究中,通过Illumina短读测序在两个独立实验中对T1190及其非转基因野生型PinS(‘Pinova’和‘Idared’的F1后代)的基因组进行了测序,T1190的平均测序深度为182×,PinS的平均测序深度为167×。测序揭示了8450条读数,其中包含与植物转化载体≥20 bp相同的序列。这些读数被组装成125个重叠群,通过五步程序检查它们是否包含转基因插入片段。一个重叠群的序列代表了T1190第4号染色体上已知的T-DNA插入。其余重叠群的序列要么在T1190和PinS中均有出现,其与载体具有序列同一性的部分在苹果参考基因组中也均有出现,要么似乎是由内生污染而非额外的转基因插入导致的。因此,我们得出结论,转基因苹果植株T1190仅在第4号染色体上有一个转基因插入,未显示转化载体的进一步部分插入。登录号:JQ974028.1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/8386123/532c978325fd/fpls-12-715737-g001.jpg

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