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黄瓜花叶病毒诱导的香蕉基因沉默。

Cucumber mosaic virus-induced gene silencing in banana.

机构信息

Agricultural Biotechnology Research Center, Academia Sinica, No. 128, Section 2, Academia Road, Nankang District, Taipei, 11529, Taiwan.

Department of Plant Pathology and Microbiology, National Taiwan University, No. 1, Section 4, Roosevelt Road, Da'an District, Taipei, 10617, Taiwan.

出版信息

Sci Rep. 2019 Aug 9;9(1):11553. doi: 10.1038/s41598-019-47962-3.

Abstract

Banana (Musa spp.) is one of the world's most important staple and cash crops. Despite accumulating genetic and transcriptomic data, low transformation efficiency in agronomically important Musa spp. render translational researches in banana difficult by using conventional knockout approaches. To develop tools for translational research in bananas, we developed a virus induced-gene silencing (VIGS) system based on a banana-infecting cucumber mosaic virus (CMV) isolate, CMV 20. CMV 20 genomic RNA 1, 2, and 3, were separately cloned in Agrobacterium pJL89 binary vectors, and a cloning site was introduced on RNA 2 immediately after the 2a open reading frame to insert the gene targeted for silencing. An efficient Agrobacterium inoculation method was developed for banana, which enabled the CMV 20 VIGS vector infection rate to reach 95% in our experiments. CMV 20-based silencing of Musa acuminata cv. Cavendish (AAA group) glutamate 1-semialdehyde aminotransferase (MaGSA) produced a typical chlorotic phenotype and silencing of M. acuminata phytoene desaturase (MaPDS) produced a photobleachnig phenotype. We show this approach efficiently reduced GSA and PDS transcripts to 10% and 18% of the control, respectively. The high infection rate and extended silencing of this VIGS system will provide an invaluable tool to accelerate functional genomic studies in banana.

摘要

香蕉(Musa spp.)是世界上最重要的主食和经济作物之一。尽管积累了大量的遗传和转录组数据,但在农艺上重要的 Musa spp.中转化效率低,使得通过传统的敲除方法难以在香蕉中进行转化研究。为了开发香蕉转化研究的工具,我们开发了一种基于感染香蕉的黄瓜花叶病毒(CMV)分离物 CMV 20 的病毒诱导基因沉默(VIGS)系统。CMV 20 的基因组 RNA1、2 和 3 分别克隆在农杆菌 pJL89 双元载体中,在 RNA2 的 2a 开放阅读框之后立即引入一个克隆位点,以插入用于沉默的目标基因。我们开发了一种有效的香蕉农杆菌接种方法,使 CMV 20 VIGS 载体的感染率在我们的实验中达到 95%。基于 CMV 20 的 Musa acuminata cv. Cavendish(AAA 组)谷氨酸 1-半醛氨基转移酶(MaGSA)沉默产生了典型的黄化表型,而 M. acuminata 类胡萝卜素脱饱和酶(MaPDS)的沉默产生了光漂白表型。我们表明,这种方法可将 GSA 和 PDS 转录物分别有效降低至对照的 10%和 18%。该 VIGS 系统的高感染率和延长的沉默时间将为加速香蕉功能基因组研究提供宝贵的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c04a/6689018/a02a33a09924/41598_2019_47962_Fig1_HTML.jpg

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