Kopischke Sarah, Schüßler Esther, Althoff Felix, Zachgo Sabine
Botany Department, School of Biology/Chemistry, Osnabrueck University, Osnabrueck, Germany.
Plant Methods. 2017 Mar 29;13:20. doi: 10.1186/s13007-017-0167-5. eCollection 2017.
The liverwort occupies a crucial position in land plant evolution and provides the opportunity to investigate adaptations to a terrestrial plant life style. Marchantia reverse genetic analyses have thus far been conducted by employing a homologous recombination approach, which yields an efficiency of around 3%. Availability of the characterized and suitable endogenous Mp promoter prompted us to establish the TALEN gene targeting technique for Marchantia.
Here, two different TALEN techniques, using custom and self-assembled TALEN constructs, were applied and compared. The Mp gene was selected as a candidate gene, as the respective knockout mutant has been shown to lack air chamber formation, representing an easily traceable phenotype. We demonstrate that both TALEN approaches are successful in Marchantia yielding high gene targeting efficiencies of over 20%. Investigation of selected G1 up to G4 generations proved the stability of the knockout mutants. In 392 analyzed T1 plants, no additional phenotypes were observed and only one chimeric knockout plant was detected after an extended cultivation period. Interestingly, two out of the 24 sequenced mutants harbored indels causing in-frame mutations and revealed novel Mp-related phenotypes. This demonstrates the potential to detect crucial amino acids and motives of targeted proteins, which is of special interest for essential genes where full knockouts are lethal. The FastTALE™ TALEN assembly kit enables the rapid assembly and ligation of the TALEN arms within half a day. For transformations, custom and assembled constructs were subcloned into Marchantia binary vectors possessing the Mp promoter.
Considering time, costs and practicability, the assembly TALEN approach represents a rapid and highly efficient gene targeting system to generate Marchantia knockout mutants, which can be further adapted for future advanced genome-editing applications.
地钱在陆地植物进化中占据关键地位,为研究适应陆地植物生活方式提供了契机。迄今为止,对地钱进行反向遗传分析采用的是同源重组方法,其效率约为3%。已鉴定且合适的内源性Mp启动子的可得性促使我们为地钱建立TALEN基因靶向技术。
在此,应用并比较了两种不同的TALEN技术,即使用定制和自组装TALEN构建体的技术。选择Mp基因作为候选基因,因为已证明相应的敲除突变体缺乏气室形成,这是一种易于追踪的表型。我们证明,两种TALEN方法在地钱中均成功,产生了超过20%的高基因靶向效率。对选定的G1至G4代的研究证明了敲除突变体的稳定性。在392株分析的T1植株中,未观察到其他表型,在延长培养期后仅检测到一株嵌合敲除植株。有趣的是,在24个测序突变体中有两个存在导致框内突变的插入缺失,并揭示了新的与Mp相关的表型。这证明了检测靶向蛋白质关键氨基酸和基序的潜力,这对于完全敲除致死的必需基因特别有意义。FastTALE™ TALEN组装试剂盒能够在半天内快速组装并连接TALEN臂。对于转化,将定制和组装的构建体亚克隆到具有Mp启动子的地钱二元载体中。
考虑到时间、成本和实用性,组装TALEN方法是一种快速且高效的基因靶向系统,可用于生成地钱敲除突变体,该系统可进一步适用于未来先进的基因组编辑应用。