The Identification and Comparative Analysis of Non-Coding RNAs in Spores and Mycelia of Penicillium expansum
-
Published:2023-10-09
Issue:10
Volume:9
Page:999
-
ISSN:2309-608X
-
Container-title:Journal of Fungi
-
language:en
-
Short-container-title:JoF
Author:
Lai Tongfei1, Yu Qinru1, Pan Jingjing1, Wang Jingjing1, Tang Zhenxing2ORCID, Bai Xuelian1, Shi Lue1, Zhou Ting1
Affiliation:
1. College of Life and Environmental Science, Hangzhou Normal University, Hangzhou 310036, China 2. School of Culinary Arts, Tourism College of Zhejiang, Hangzhou 311231, China
Abstract
Penicillium expansum is the most popular post-harvest pathogen and causes blue mold disease in pome fruit and leads to significant economic losses worldwide every year. However, the fundamental regulation mechanisms of growth in P. expansum are unclear. Recently, non-coding RNAs (ncRNAs) have attracted more attention due to critical roles in normalizing gene expression and maintaining cellular genotypes in organisms. However, the research related to ncRNAs in P. expansum have not been reported. Therefore, to provide an overview of ncRNAs on composition, distribution, expression changes, and potential targets in the growth process, a comparative transcriptomic analysis was performed on spores and mycelia of P. expansum in the present study. A total of 2595 novel mRNAs, 3362 long non-coding RNAs (lncRNAs), 10 novel microRNAs (miRNAs), 86 novel small interfering RNAs (siRNAs), and 11,238 circular RNAs (circRNAs) were predicted and quantified. Of these, 1482 novel mRNAs, 5987 known mRNAs, 2047 lncRNAs, 40 miRNAs, 38 novel siRNAs, and 9235 circRNAs were differentially expressed (DE) in response to the different development stages. Afterward, the involved functions and pathways of DE RNAs were revealed via Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) database enrichment analysis. The interaction networks between mRNAs, lncRNAs, and miRNAs were also predicted based on their correlation coefficient of expression profiles. Among them, it was found that miR168 family members may play important roles in fungal growth due to their central location in the network. These findings will contribute to a better understanding on regulation machinery at the RNA level on fungal growth and provide a theoretical basis to develop novel control strategies against P. expansum.
Funder
Zhejiang Provincial Natural Science Foundation of China
Subject
Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)
Reference85 articles.
1. Dissection of patulin biosynthesis, spatial control and regulation mechanism in Penicillium expansum;Li;Environ. Microbiol.,2019 2. Li, C.Z., Zhang, F.M., Gan, D., Wang, C.Y., Zhou, H., Yin, T.P., and Cai, L. (2023). Secondary metabolites isolated from Penicillium expansum and their chemotaxonomic value. Biochem. Syst. Ecol., 107. 3. Riachy, R.A., Strub, C., Durand, N., Guibert, B., Guichard, H., Constancias, F., Chochois, V., Lopez-Lauri, F., Fontana, A., and Schorr-Galindo, S. (2021). Microbiome status of cider-apples, from orchard to processing, with a special focus on Penicillium expansum occurrence and patulin contamination. J. Fungi, 7. 4. Diversity and metabolomics characterization of Penicillium expansum isolated from apples grown in Argentina and Spain;Maldonado;Fungal Biol.,2022 5. Yu, L.L., Qiao, N.Z., Zhao, J.X., Zhang, H., Tian, F.W., Zhai, Q.X., and Chen, W. (2020). Postharvest control of Penicillium expansum in fruits: A review. Food Biosci., 36.
|
|