Discovery of microRNA-like Small RNAs in Pathogenic Plant Fungus Verticillium nonalfalfae Using High-Throughput Sequencing and qPCR and RLM-RACE Validation
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
34110
Slovenian Research Agency
P4-0077
Slovenian Research Agency
PubMed
35055083
PubMed Central
PMC8778906
DOI
10.3390/ijms23020900
PII: ijms23020900
Knihovny.cz E-zdroje
- Klíčová slova
- RNA interference, Verticillium nonalfalfae, fungal pathogen, microRNA-like RNAs, plant-pathogen interactions,
- MeSH
- Ascomycota genetika MeSH
- fungální RNA * MeSH
- fylogeneze MeSH
- genová ontologie MeSH
- interakce hostitele a patogenu MeSH
- konformace nukleové kyseliny MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- malá nekódující RNA genetika MeSH
- mikro RNA genetika MeSH
- nemoci rostlin mikrobiologie MeSH
- regulace genové exprese u hub MeSH
- reprodukovatelnost výsledků MeSH
- stanovení celkové genové exprese MeSH
- výpočetní biologie metody MeSH
- vysoce účinné nukleotidové sekvenování * MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- fungální RNA * MeSH
- malá nekódující RNA MeSH
- mikro RNA MeSH
Verticillium nonalfalfae (V. nonalfalfae) is one of the most problematic hop (Humulus lupulus L.) pathogens, as the highly virulent fungal pathotypes cause severe annual yield losses due to infections of entire hop fields. In recent years, the RNA interference (RNAi) mechanism has become one of the main areas of focus in plant-fungal pathogen interaction studies and has been implicated as one of the major contributors to fungal pathogenicity. MicroRNA-like RNAs (milRNAs) have been identified in several important plant pathogenic fungi; however, to date, no milRNA has been reported in the V. nonalfalfae species. In the present study, using a high-throughput sequencing approach and extensive bioinformatics analysis, a total of 156 milRNA precursors were identified in the annotated V. nonalfalfae genome, and 27 of these milRNA precursors were selected as true milRNA candidates, with appropriate microRNA hairpin secondary structures. The stem-loop RT-qPCR assay was used for milRNA validation; a total of nine V. nonalfalfae milRNAs were detected, and their expression was confirmed. The milRNA expression patterns, determined by the absolute quantification approach, imply that milRNAs play an important role in the pathogenicity of highly virulent V. nonalfalfae pathotypes. Computational analysis predicted milRNA targets in the V. nonalfalfae genome and in the host hop transcriptome, and the activity of milRNA-mediated RNAi target cleavage was subsequently confirmed for two selected endogenous fungal target gene models using the 5' RLM-RACE approach.
Department of Agronomy Biotechnical Faculty University of Ljubljana 1000 Ljubljana Slovenia
Plant Protection Department Slovenian Institute of Hop Research and Brewing 3310 Žalec Slovenia
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