Underwood William
United States Department of Agriculture-Agricultural Research Service Sunflower & Plant Biology Research Unit, Edward T. Schafer Agricultural Research Center, Fargo, ND 58102, U.S.A.
Mol Plant Microbe Interact. 2022 May;35(5):393-400. doi: 10.1094/MPMI-09-21-0240-R. Epub 2022 Apr 20.
The PENETRATION 3 (PEN3) ATP binding cassette (ABC) transporter contributes to penetration resistance against nonadapted powdery mildew fungi and is targeted to papillae deposited at sites of interaction with the fungus. Timely recruitment of PEN3 and other components of penetration resistance to the host-pathogen interface is important for successful defense against this biotrophic pathogen. A forward genetic screen was previously carried out to identify mutants that mistarget the PEN3 transporter or fail to accumulate PEN3 at sites of attempted powdery mildew penetration. This study focuses on PEN3 mistargeting in the () mutant and identification of the causal gene. In the mutant, PEN3 accumulates within the endomembrane system in an apparently abnormal endoplasmic reticulum and is not exported into papillae at powdery mildew penetration sites. This targeting defect compromises defenses at the host-pathogen interface, resulting in increased penetration success by a nonadapted powdery mildew. Genetic mapping identified as an allele of (), a gene encoding a GDSL-lipase/esterase family protein that is involved in maintaining normal morphology and organization of multiple endomembrane compartments. Genetic complementation confirmed that mutation in is responsible for the PEN3 targeting and powdery mildew penetration resistance defects in . These results reinforce the importance of endomembrane trafficking in resistance to haustorium-forming phytopathogens such as powdery mildew fungi.[Formula: see text] Copyright © 2022 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
渗透3(PEN3)ATP结合盒(ABC)转运蛋白有助于抵抗非适应性白粉病菌的侵入,并且定位于与真菌相互作用位点处沉积的乳突。及时将PEN3和其他抗侵入成分募集到宿主-病原体界面对于成功抵御这种活体营养型病原体至关重要。先前进行了正向遗传学筛选,以鉴定将PEN3转运蛋白错误定位或在白粉病菌试图侵入的位点未能积累PEN3的突变体。本研究聚焦于()突变体中PEN3的错误定位以及致病基因的鉴定。在该突变体中,PEN3在内膜系统中于明显异常的内质网内积累,并且在白粉病菌侵入位点未输出到乳突中。这种定位缺陷损害了宿主-病原体界面处的防御,导致非适应性白粉病菌的侵入成功率增加。遗传定位确定为()的一个等位基因,()是一个编码GDSL脂肪酶/酯酶家族蛋白的基因,该蛋白参与维持多个内膜区室的正常形态和组织。遗传互补证实,中的突变是导致中PEN3定位和白粉病菌侵入抗性缺陷的原因。这些结果强化了内膜运输在抵抗形成吸器的植物病原体(如白粉病菌)中的重要性。[公式:见正文] 版权所有© 2022作者。这是一篇根据知识共享署名-非商业性使用-禁止演绎4.0国际许可协议分发的开放获取文章。