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致病疫霉AGO1结合来自效应蛋白基因和转座元件的微小RNA和小RNA。

Phytophthora infestans Argonaute 1 binds microRNA and small RNAs from effector genes and transposable elements.

作者信息

Åsman Anna K M, Fogelqvist Johan, Vetukuri Ramesh R, Dixelius Christina

机构信息

Department of Plant Biology, Swedish University of Agricultural Sciences, Uppsala BioCenter, Linnéan Center for Plant Biology, PO Box 7080, SE-75007, Uppsala, Sweden.

Department of Plant Protection Biology, Swedish University of Agricultural Sciences, Resistance Biology Unit, PO Box 102, SE-23053, Alnarp, Sweden.

出版信息

New Phytol. 2016 Aug;211(3):993-1007. doi: 10.1111/nph.13946. Epub 2016 Mar 24.

Abstract

Phytophthora spp. encode large sets of effector proteins and distinct populations of small RNAs (sRNAs). Recent evidence has suggested that pathogen-derived sRNAs can modulate the expression of plant defense genes. Here, we studied the sRNA classes and functions associated with Phytophthora infestans Argonaute (Ago) proteins. sRNAs were co-immunoprecipitated with three PiAgo proteins and deep sequenced. Twenty- to twenty-two-nucleotide (nt) sRNAs were identified as the main interaction partners of PiAgo1 and high enrichment of 24-26-nt sRNAs was seen in the PiAgo4-bound sample. The frequencies and sizes of transposable element (TE)-derived sRNAs in the different PiAgo libraries suggested diversified roles of the PiAgo proteins in the control of different TE classes. We further provide evidence for the involvement of PiAgo1 in the P. infestans microRNA (miRNA) pathway. Protein-coding genes are probably regulated by the shared action of PiAgo1 and PiAgo5, as demonstrated by analysis of differential expression. An abundance of sRNAs from genes encoding host cell death-inducing Crinkler (CRN) effectors was bound to PiAgo1, implicating this protein in the regulation of the expanded CRN gene family. The data suggest that PiAgo1 plays an essential role in gene regulation and that at least two RNA silencing pathways regulate TEs in the plant-pathogenic oomycete P. infestans.

摘要

疫霉属物种编码大量效应蛋白和不同群体的小RNA(sRNA)。最近的证据表明,病原体来源的sRNA可以调节植物防御基因的表达。在这里,我们研究了与致病疫霉AGO蛋白相关的sRNA类别和功能。sRNA与三种致病疫霉AGO蛋白进行共免疫沉淀并进行深度测序。20至22个核苷酸(nt)的sRNA被鉴定为致病疫霉AGO1的主要相互作用伙伴,在与致病疫霉AGO4结合的样本中观察到24至26个nt的sRNA高度富集。不同致病疫霉AGO文库中转座元件(TE)来源的sRNA的频率和大小表明致病疫霉AGO蛋白在控制不同TE类别中具有多样化的作用。我们进一步提供了致病疫霉AGO1参与致病疫霉微小RNA(miRNA)途径的证据。通过差异表达分析表明,蛋白质编码基因可能受致病疫霉AGO1和致病疫霉AGO5共同作用的调控。来自编码诱导宿主细胞死亡的卷曲蛋白(CRN)效应蛋白的基因的大量sRNA与致病疫霉AGO1结合,表明该蛋白参与了扩展的CRN基因家族的调控。数据表明致病疫霉AGO1在基因调控中起重要作用,并且至少有两条RNA沉默途径调控植物致病卵菌致病疫霉中的TE。

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