Structural features of T-DNA that induce transcriptional gene silencing during agroinfiltration.

IF 1.4 4区 生物学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Emi Iida, Kazunori Kuriyama, Midori Tabara, Atsushi Takeda, Nobuhiro Suzuki, Hiromitsu Moriyama, Toshiyuki Fukuhara
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引用次数: 0

Abstract

Agrobacterium tumefaciens (Rhizobium radiobacter) is used for the transient expression of foreign genes by the agroinfiltration method, but the introduction of foreign genes often induces transcriptional and/or post-transcriptional gene silencing (TGS and/or PTGS). In this study, we characterized the structural features of T-DNA that induce TGS during agroinfiltration. When A. tumefaciens cells harboring an empty T-DNA plasmid containing the cauliflower mosaic virus (CaMV) 35S promoter were infiltrated into the leaves of Nicotiana benthamiana line 16c with a GFP gene over-expressed under the control of the same promoter, no small interfering RNAs (siRNAs) were derived from the GFP sequence. However, siRNAs derived from the CaMV 35S promoter were detected, indicating that TGS against the GFP gene was induced. When the GFP gene was inserted into the T-DNA plasmid, PTGS against the GFP gene was induced whereas TGS against the CaMV 35S promoter was suppressed. We also showed the importance of terminator sequences in T-DNA for gene silencing. Therefore, depending on the combination of promoter, terminator and coding sequences on T-DNA and the host nuclear genome, either or both TGS and/or PTGS could be induced by agroinfiltration. Furthermore, we showed the possible involvement of three siRNA-producing Dicers (DCL2, DCL3 and DCL4) in the induction of TGS by the co-agroinfiltration method. Especially, DCL2 was probably the most important among them in the initial step of TGS induction. These results are valuable for controlling gene expression by agroinfiltration.

T-DNA 的结构特征在农业渗透过程中诱导转录基因沉默。
农杆菌(Rhizobium radiobacter)通过农用渗透法用于外来基因的瞬时表达,但外来基因的引入往往会诱导转录和/或转录后基因沉默(TGS 和/或 PTGS)。在这项研究中,我们研究了T-DNA在农渗过程中诱导TGS的结构特征。当含有花椰菜花叶病毒(CaMV)35S启动子的空T-DNA质粒的A.tumefaciens细胞被浸润到带有在同一启动子控制下过度表达的GFP基因的Nicotiana benthamiana品系16c的叶片中时,没有从GFP序列衍生出小干扰RNA(siRNA)。然而,检测到了来自 CaMV 35S 启动子的 siRNA,这表明针对 GFP 基因的 TGS 被诱导了。当 GFP 基因插入 T-DNA 质粒时,针对 GFP 基因的 PTGS 被诱导,而针对 CaMV 35S 启动子的 TGS 被抑制。我们还发现了 T-DNA 中终止子序列对基因沉默的重要性。因此,根据 T-DNA 和宿主核基因组上启动子、终止子和编码序列的组合,农渗可以诱导 TGS 和/或 PTGS。此外,我们还发现三种能产生 siRNA 的 Dicers(DCL2、DCL3 和 DCL4)可能参与了共同农渗法诱导 TGS 的过程。特别是,DCL2 可能是其中对 TGS 诱导起始阶段最重要的一个。这些结果对通过农渗法控制基因表达很有价值。
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来源期刊
Plant Biotechnology
Plant Biotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-PLANT SCIENCES
CiteScore
2.90
自引率
18.80%
发文量
45
审稿时长
6-12 weeks
期刊介绍: Plant Biotechnology is an international, open-access, and online journal, published every three months by the Japanese Society for Plant Biotechnology. The journal, first published in 1984 as the predecessor journal, “Plant Tissue Culture Letters” and became its present form in 1997 when the society name was renamed to Japanese Society for Plant Cell and Molecular Biology, publishes findings in the areas from basic- to application research of plant biotechnology. The aim of Plant Biotechnology is to publish original and high-impact papers, in the most rapid turnaround time for reviewing, on the plant biotechnology including tissue culture, production of specialized metabolites, transgenic technology, and genome editing technology, and also on the related research fields including molecular biology, cell biology, genetics, plant breeding, plant physiology and biochemistry, metabolic engineering, synthetic biology, and bioinformatics.
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