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致病疫霉的特异性磷酸化模式及新的潜在调控靶点。

Phytophthora infestans specific phosphorylation patterns and new putative control targets.

作者信息

Frades Itziar, Andreasson Erik

机构信息

Department of Plant Protection Biology, Swedish University of Agricultural Sciences, Alnarp, SE-230 53, Sweden.

Department of Plant Protection Biology, Swedish University of Agricultural Sciences, Alnarp, SE-230 53, Sweden.

出版信息

Fungal Biol. 2016 Apr;120(4):631-644. doi: 10.1016/j.funbio.2016.01.003. Epub 2016 Jan 18.

Abstract

In this study we applied biomathematical searches of gene regulatory mechanisms to learn more about oomycete biology and to identify new putative targets for pesticides or biological control against Phytophthora infestans. First, oomycete phylum-specific phosphorylation motifs were found by discriminative n-gram analysis. We found 11.600 P. infestans specific n-grams, mapping 642 phosphoproteins. The most abundant group among these related to phosphatidylinositol metabolism. Due to the large number of possible targets found and our hypothesis that multi-level control is a sign of usefulness as targets for intervention, we identified overlapping targets with a second screen. This was performed to identify proteins dually regulated by small RNA and phosphorylation. We found 164 proteins to be regulated by both sRNA and phosphorylation and the dominating functions where phosphatidylinositol signalling/metabolism, endocytosis, and autophagy. Furthermore we performed a similar regulatory study and discriminative n-gram analysis of proteins with no clear orthologs in other species and proteins that are known to be unique to P. infestans such as the RxLR effectors, Crinkler (CRN) proteins and elicitins. We identified CRN proteins with specific phospho-motifs present in all life stages. PITG_12626, PITG_14042 and PITG_23175 are CRN proteins that have species-specific phosphorylation motifs and are subject to dual regulation.

摘要

在本研究中,我们应用基因调控机制的生物数学搜索方法,以更多地了解卵菌生物学,并确定针对致病疫霉的农药或生物防治的新潜在靶点。首先,通过判别性n元语法分析发现了卵菌门特异性磷酸化基序。我们发现了11600个致病疫霉特异性n元语法,对应642个磷酸化蛋白。其中最丰富的一组与磷脂酰肌醇代谢有关。由于发现了大量可能的靶点,且我们假设多级调控是作为干预靶点有用性的一个标志,因此我们通过第二次筛选确定了重叠靶点。这样做是为了鉴定受小RNA和磷酸化双重调控的蛋白质。我们发现164种蛋白质受sRNA和磷酸化共同调控,主要功能是磷脂酰肌醇信号传导/代谢、内吞作用和自噬。此外,我们对在其他物种中没有明确直系同源物的蛋白质以及已知为致病疫霉特有的蛋白质(如RxLR效应子、卷曲蛋白(CRN)和激发素)进行了类似的调控研究和判别性n元语法分析。我们鉴定出在所有生命阶段都存在特定磷酸基序的CRN蛋白。PITG_12626、PITG_14042和PITG_23175是具有物种特异性磷酸化基序且受到双重调控的CRN蛋白。

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