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在多年生果树上使用锌指核酸酶进行靶向诱变。

Targeted mutagenesis using zinc-finger nucleases in perennial fruit trees.

作者信息

Peer Reut, Rivlin Gil, Golobovitch Sara, Lapidot Moshe, Gal-On Amit, Vainstein Alexander, Tzfira Tzvi, Flaishman Moshe A

机构信息

Institute of Plant Sciences, Agricultural Research Organization, P.O. Box 6, 50250, Bet-Dagan, Israel.

出版信息

Planta. 2015 Apr;241(4):941-51. doi: 10.1007/s00425-014-2224-x. Epub 2014 Dec 21.

Abstract

Targeting a gene in apple or fig with ZFN, introduced by transient or stable transformation, should allow genome editing with high precision to advance basic science and breeding programs. Genome editing is a powerful tool for precise gene manipulation in any organism; it has recently been shown to be of great value for annual plants. Classical breeding strategies using conventional cross-breeding and induced mutations have played an important role in the development of new cultivars in fruit trees. However, fruit-tree breeding is a lengthy process with many limitations. Efficient and widely applied methods for targeted modification of fruit-tree genomes are not yet available. In this study, transgenic apple and fig lines carrying a zinc-finger nuclease (ZFNs) under the control of a heat-shock promoter were developed. Editing of a mutated uidA gene, following expression of the ZFN genes by heat shock, was confirmed by GUS staining and PCR product sequencing. Finally, whole plants with a repaired uidA gene due to deletion of a stop codon were regenerated. The ZFN-mediated gene modifications were stable and passed onto regenerants from ZFN-treated tissue cultures. This is the first demonstration of efficient and precise genome editing, using ZFN at a specific genomic locus, in two different perennial fruit trees-apple and fig. We conclude that targeting a gene in apple or fig with a ZFN introduced by transient or stable transformation should allow knockout of a gene of interest. Using this technology for genome editing allows for marker gene-independent and antibiotic selection-free genome engineering with high precision in fruit trees to advance basic science as well as nontransgenic breeding programs.

摘要

通过瞬时或稳定转化引入锌指核酸酶(ZFN)靶向苹果或无花果中的基因,应能实现高精度的基因组编辑,从而推动基础科学研究和育种计划。基因组编辑是在任何生物体中进行精确基因操作的强大工具;最近已证明其对一年生植物具有重要价值。利用传统杂交育种和诱导突变的经典育种策略在果树新品种的培育中发挥了重要作用。然而,果树育种是一个漫长的过程,存在诸多限制。目前尚未有高效且广泛应用的果树基因组靶向修饰方法。在本研究中,我们培育了在热激启动子控制下携带锌指核酸酶(ZFNs)的转基因苹果和无花果品系。通过热激表达ZFN基因后,经GUS染色和PCR产物测序证实了突变的uidA基因被编辑。最终,由于终止密码子缺失而使uidA基因得到修复的完整植株得以再生。ZFN介导的基因修饰是稳定的,并传递给了经ZFN处理的组织培养再生植株。这是首次在两种不同的多年生果树——苹果和无花果中,利用ZFN在特定基因组位点进行高效且精确的基因组编辑的证明。我们得出结论,通过瞬时或稳定转化引入ZFN靶向苹果或无花果中的基因应能敲除感兴趣的基因。利用这项技术进行基因组编辑可实现果树中高精度的无标记基因和无抗生素选择的基因组工程,以推动基础科学研究以及非转基因育种计划。

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