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靶向……的CRISPR/Cas9机制的瞬时表达增强了……中的防御反应。

Transient Expression of CRISPR/Cas9 Machinery Targeting Enhances Defense Response in .

作者信息

Fister Andrew S, Landherr Lena, Maximova Siela N, Guiltinan Mark J

机构信息

Department of Plant Science, Pennsylvania State University, University Park, PA, United States.

Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, PA, United States.

出版信息

Front Plant Sci. 2018 Mar 2;9:268. doi: 10.3389/fpls.2018.00268. eCollection 2018.

Abstract

, the source of cocoa, suffers significant losses to a variety of pathogens resulting in reduced incomes for millions of farmers in developing countries. Development of disease resistant cacao varieties is an essential strategy to combat this threat, but is limited by sources of genetic resistance and the slow generation time of this tropical tree crop. In this study, we present the first application of genome editing technology in cacao, using Agrobacterium-mediated transient transformation to introduce CRISPR/Cas9 components into cacao leaves and cotyledon cells. As a first proof of concept, we targeted the cacao gene, a suppressor of the defense response. After demonstrating activity of designed single-guide RNAs (sgRNA) , we used to introduce a CRISPR/Cas9 system into leaf tissue, and identified the presence of deletions in 27% of copies in the treated tissues. The edited tissue exhibited an increased resistance to infection with the cacao pathogen and elevated expression of downstream defense genes. Analysis of off-target mutagenesis in sequences similar to sgRNA target sites using high-throughput sequencing did not reveal mutations above background sequencing error rates. These results confirm the function of NPR3 as a repressor of the cacao immune system and demonstrate the application of CRISPR/Cas9 as a powerful functional genomics tool for cacao. Several stably transformed and genome edited somatic embryos were obtained via -mediated transformation, and ongoing work will test the effectiveness of this approach at a whole plant level.

摘要

可可的来源遭受各种病原体的重大损失,导致发展中国家数百万农民收入减少。培育抗病可可品种是应对这一威胁的一项重要战略,但受到遗传抗性来源和这种热带树木作物生长周期长的限制。在本研究中,我们展示了基因组编辑技术在可可中的首次应用,利用农杆菌介导的瞬时转化将CRISPR/Cas9组件导入可可叶片和子叶细胞。作为概念验证,我们靶向了可可基因,一种防御反应的抑制因子。在证明设计的单向导RNA(sgRNA)的活性后,我们使用它将CRISPR/Cas9系统导入叶片组织,并在处理过的组织中27%的拷贝中鉴定出缺失的存在。编辑后的组织对可可病原体感染的抗性增强,下游防御基因的表达升高。使用高通量测序分析与sgRNA靶位点相似的序列中的脱靶诱变,未发现高于背景测序错误率的突变。这些结果证实了NPR3作为可可免疫系统抑制因子的功能,并证明了CRISPR/Cas9作为可可强大的功能基因组学工具的应用。通过介导的转化获得了几个稳定转化和基因组编辑的体细胞胚,正在进行的工作将在整株水平上测试这种方法的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc1/5841092/2fc440cf569e/fpls-09-00268-g0001.jpg

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