全面分析小麦-三尖杉菌相互作用过程中参与抗性和致病的发夹式小 RNA。

IF 5.4 2区 生物学 Q1 PLANT SCIENCES Physiologia plantarum Pub Date : 2024-09-01 DOI:10.1111/ppl.14516
Uzma Afreen, Anjali Pandey, Shailendra Kumar Jha, Manish Kumar, Kunal Mukhopadhyay
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引用次数: 0

摘要

由真菌 Puccinia triticina(Pt)引起的小麦叶锈病严重影响面包小麦(Triticum aestivum L.)的籽粒质量和产量。 发夹型小 RNA,如 micro(mi)RNA 及其变体[包括 isomiRNAs(isomiRs)和 microRNA-like RNAs(milRNAs)],连同其相应的靶基因,赋予叶锈病抗病性,以及两种相互作用物种的发育和发展。然而,对其调控网络的了解仍然不足。研究人员从小麦 sRNA 文库的诱导读数中发现了 13 个差异表达的新型 miRNA,包括 2 个异RNA 和 3 个 milRNA,并分别预测了小麦和铂中的 5,393 和 1,275 个候选靶基因。功能注释表明,小麦起源的 miRNAs/isomiRs 参与了抗性,而铂起源的 milRNAs 传导了致病机理。通过降解组文库筛选,确认了已鉴定的milRNAs--Tae-Pt-milR5、Tae-Pt-milR12和Tae-Pt-milR14b及其在Pt靶基因MEP5上的裂解位点,这表明Pt毒力基因在小麦宿主中的跨域转位。miRNAs/isomiRs-靶基因的共表达分析为防治叶锈病提供了启示,而milRNAs-靶基因对的共表达分析则反映了Pt的致病程度,在分析时间点的表达水平各不相同。该分析确定了对叶锈病有响应的候选发夹状 sRNA--小麦中的 Tae-miR8、Tae-Pt-miR12、Tae-Pt-miR14a 和 Tae-Pt-miR14b,以及铂中的 Tae-Pt-milR12。此外,研究还发现了一些关键的发夹状 sRNAs 及其有望用于未来生物技术干预以增强抗逆性的靶标。
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Comprehensive analysis of hairpin small RNAs involved in resistance and pathogenesis during wheat-Puccinia triticina interactions.

Wheat leaf rust, caused by the fungus Puccinia triticina (Pt), severely affects the grain quality and quantity of bread wheat (Triticum aestivum L.). Hairpin small(s)RNAs, like micro(mi)RNAs and their variants [including isomiRNAs (isomiRs) and microRNA-like RNAs (milRNAs)], along with their corresponding target genes, bestow leaf rust disease resistance, development and progression from both interacting species. However, the regulatory networks remain inadequately understood. Thirteen differentially expressed novel miRNAs, including two isomiRs and three milRNAs were discerned from induced reads of wheat sRNA libraries, and a further 5,393 and 1,275 candidate target genes were predicted in wheat and Pt, respectively. Functional annotation divulged that wheat-originated miRNAs/isomiRs were involved in resistance, while Pt-derived milRNAs imparted pathogenesis. The identified milRNAs- Tae-Pt-milR5, Tae-Pt-milR12, and Tae-Pt-milR14b and their cleavage sites on Pt target gene MEP5 were confirmed through degradome library screening, suggesting cross-kingdom translocation of Pt virulent genes in wheat host. Co-expression analysis of miRNAs/isomiRs-target genes provided insights into combating leaf rust disease, while co-expression analysis of milRNAs-target gene pairs reflected the extent of pathogenicity exerted by Pt with varied expression levels at the analyzed time points. The analysis pinpointed leaf rust-responsive candidate hairpin sRNAs- Tae-miR8, Tae-Pt-miR12, Tae-Pt-miR14a, and Tae-Pt-miR14b in wheat and Tae-Pt-milR12 in Pt. This study provides new insights into the hairpin sRNAs involved in the resistance and pathogenesis of wheat and Pt, respectively. Furthermore, crucial hairpin sRNAs and their promising targets for future biotechnological interventions to augment stress resilience have been identified.

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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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