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利用 CRISPR/Cas9 技术在小麦中高效生成稳定、可遗传的基因编辑。

Efficient generation of stable, heritable gene edits in wheat using CRISPR/Cas9.

机构信息

The John Bingham Laboratory, NIAB, Huntingdon Road, Cambridge, CB3 0LE, UK.

出版信息

BMC Plant Biol. 2018 Oct 3;18(1):215. doi: 10.1186/s12870-018-1433-z.

Abstract

BACKGROUND

The use of CRISPR/Cas9 systems could prove to be a valuable tool in crop research, providing the ability to fully knockout gene function in complex genomes or to precisely adjust gene function by knockout of individual alleles.

RESULTS

We compare gene editing in hexaploid wheat (Triticum aestivum) with diploid barley (Hordeum vulgare), using a combination of single genome and tri-genome targeting. High efficiency gene editing, 11-17% for single genome targeted guides and 5% for tri-genome targeted guides, was achieved in wheat using stable Agrobacterium-mediated transformation. Gene editing in wheat was shown to be predominantly heterozygous, edits were inherited in a Mendelian fashion over multiple generations and no off-target effects were observed. Comparison of editing between the two species demonstrated that more stable, heritable edits were produced in wheat, whilst barley exhibited continued and somatic editing.

CONCLUSION

Our work shows the potential to obtain stable edited transgene-free wheat lines in 36 weeks through only two generations and that targeted mutagenesis of individual homeologues within the wheat genome is achievable with a modest amount of effort, and without off-target mutations or the need for lengthy crossing strategies.

摘要

背景

CRISPR/Cas9 系统的使用在作物研究中可能是一种很有价值的工具,它能够在复杂基因组中完全敲除基因功能,或者通过敲除单个等位基因来精确调整基因功能。

结果

我们比较了六倍体小麦(Triticum aestivum)和二倍体大麦(Hordeum vulgare)中的基因编辑,使用了单基因组和三基因组靶向的组合。利用稳定的农杆菌介导转化,在小麦中实现了高效的基因编辑,单基因组靶向向导的编辑效率为 11-17%,三基因组靶向向导的编辑效率为 5%。在小麦中,基因编辑主要是杂合的,编辑在多个世代中以孟德尔方式遗传,并且没有观察到脱靶效应。对这两个物种的编辑比较表明,在小麦中产生了更稳定、可遗传的编辑,而大麦则表现出持续的和体细胞编辑。

结论

我们的工作表明,通过仅两代就有可能在 36 周内获得稳定的编辑无转基因小麦系,并且在小麦基因组中单个性同源基因的靶向诱变是可行的,只需少量的努力,并且没有脱靶突变或需要冗长的杂交策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9612/6171145/0ffaf9d79232/12870_2018_1433_Fig1_HTML.jpg

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