Institute of Plant Genetics, Polish Academy of Sciences, ul. Strzeszyńska 34, 60-479, Poznań, Poland.
Laboratory of Genome Biology, Institute of Molecular Biology and Biotechnology, Adam Mickiewicz University, ul. Uniwersytetu Poznańskiego 6, 61-614, Poznań, Poland.
Plant J. 2023 Dec;116(5):1421-1440. doi: 10.1111/tpj.16438. Epub 2023 Aug 30.
Despite the identification of clubroot resistance genes in various Brassica crops our understanding of the genetic basis of immunity to Plasmodiophora brassicae infection in the model plant Arabidopsis thaliana remains limited. To address this issue, we performed a screen of 142 natural accessions and identified 11 clubroot-resistant Arabidopsis lines. Genome-wide association analysis identified several genetic loci significantly linked with resistance. Three genes from two of these loci were targeted for deletion by CRISPR/Cas9 mutation in resistant accessions Est-1 and Uod-1. Deletion of Resistance to Plasmodiophora brassicae 1 (RPB1) rendered both lines susceptible to the P. brassicae pathotype P1+. Further analysis of rpb1 knock-out Est-1 and Uod-1 lines showed that the RPB1 protein is required for activation of downstream defence responses, such as the expression of phytoalexin biosynthesis gene CYP71A13. RPB1 has recently been shown to encode a cation channel localised in the endoplasmic reticulum. The clubroot susceptible Arabidopsis accession Col-0 lacks a functional RPB1 gene; when Col-0 is transformed with RPB1 expression driven by its native promoter it is capable of activating RPB1 transcription in response to infection, but this is not sufficient to confer resistance. Transient expression of RPB1 in Nicotiana tabacum induced programmed cell death in leaves. We conclude that RPB1 is a critical component of the defence response to P. brassicae infection in Arabidopsis, acting downstream of pathogen recognition but required for the elaboration of effective resistance.
尽管在各种芸薹属作物中鉴定出了根肿病抗性基因,但我们对模式植物拟南芥中对根肿菌感染的免疫遗传基础的理解仍然有限。为了解决这个问题,我们对 142 个自然群体进行了筛选,鉴定出了 11 个根肿病抗性拟南芥系。全基因组关联分析鉴定出了几个与抗性显著相关的遗传位点。从这两个位点中的两个基因通过 CRISPR/Cas9 在抗性系 Est-1 和 Uod-1 中进行突变。删除抗病基因 RPB1 使这两个系都对根肿菌 P1+生理小种敏感。对 rpb1 敲除系 Est-1 和 Uod-1 的进一步分析表明,RPB1 蛋白是激活下游防御反应所必需的,如植物抗毒素生物合成基因 CYP71A13 的表达。最近已经表明 RPB1 编码一种位于内质网中的阳离子通道。根肿病敏感的拟南芥系 Col-0 缺乏功能正常的 RPB1 基因;当 Col-0 被其天然启动子驱动的 RPB1 表达转化时,它能够激活 RPB1 转录以响应感染,但这不足以赋予抗性。在烟草中瞬时表达 RPB1 会诱导叶片程序性细胞死亡。我们得出结论,RPB1 是拟南芥对根肿菌感染防御反应的关键组成部分,作用于病原体识别的下游,但需要有效地发挥抗性。