A non-classical PUF family protein in oomycetes functions as a pre-rRNA processing regulator and a target for RNAi-based disease control
Ribosome biogenesis is an essential and tightly regulated process linked to cell proliferation and growth. However, its regulatory mechanisms in oomycetes, a group of organisms with significant agricultural and ecological importance, remain unclear. In this study, we identify Puf4, a non-classical P...
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Published in | PLoS pathogens Vol. 21; no. 7; p. e1013379 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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31.07.2025
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Abstract | Ribosome biogenesis is an essential and tightly regulated process linked to cell proliferation and growth. However, its regulatory mechanisms in oomycetes, a group of organisms with significant agricultural and ecological importance, remain unclear. In this study, we identify Puf4, a non-classical PUF (Pumilio and FBF) family RNA-binding protein that plays a conserved and crucial role in pre-rRNA processing in oomycetes. Knockout of PuPuf4 in Pythium ultimum or its ortholog PsPuf4 in Phytophthora sojae results in defective vegetative growth, impaired development, and reduced pathogenicity. Specifically, PuPuf4 binds to the H68 component of 25S rRNA, and its knockout leads to overaccumulation of rRNA processing intermediates, including 5′ETS, ITS1, and ITS2 precursors. Additionally, the AG-rich motif identified as the first binding motif of L-shaped PUF proteins, including PuPuf4, APUM24, and ScPuf6, may contribute to their specific RNA-binding affinity due to its unique structural features. Given the conserved role of Puf4 in oomycete pathogenicity, we developed the first nano-material-free dsRNA delivery system via zoospore-specific uptake, effectively attenuating virulence in Pythium aphanidermatum and Ph. sojae through RNAi targeting Puf4 . This study presents novel findings on structural and functional conservation of Puf4 and offers a promising RNAi-based strategy for controlling oomycete plant diseases. |
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AbstractList | Ribosome biogenesis is an essential and tightly regulated process linked to cell proliferation and growth. However, its regulatory mechanisms in oomycetes, a group of organisms with significant agricultural and ecological importance, remain unclear. In this study, we identify Puf4, a non-classical PUF (Pumilio and FBF) family RNA-binding protein that plays a conserved and crucial role in pre-rRNA processing in oomycetes. Knockout of
PuPuf4
in
Pythium ultimum
or its ortholog
PsPuf4
in
Phytophthora sojae
results in defective vegetative growth, impaired development, and reduced pathogenicity. Specifically, PuPuf4 binds to the H68 component of 25S rRNA, and its knockout leads to overaccumulation of rRNA processing intermediates, including 5′ETS, ITS1, and ITS2 precursors. Additionally, the AG-rich motif identified as the first binding motif of L-shaped PUF proteins, including PuPuf4, APUM24, and ScPuf6, may contribute to their specific RNA-binding affinity due to its unique structural features. Given the conserved role of
Puf4
in oomycete pathogenicity, we developed the first nano-material-free dsRNA delivery system via zoospore-specific uptake, effectively attenuating virulence in
Pythium aphanidermatum
and
Ph. sojae
through RNAi targeting
Puf4
. This study presents novel findings on structural and functional conservation of Puf4 and offers a promising RNAi-based strategy for controlling oomycete plant diseases.
Ribosome biogenesis plays a crucial role in cell growth and proliferation. However, the regulation of this process in oomycetes, an ecologically and agriculturally important group of organisms, remains largely unknown. In this study, we identified Puf4, a non-classical PUF family RNA-binding protein of oomycetes, as a key factor promoting ribosome assembly in these pathogenic organisms. When we removed
Puf4
from two harmful oomycetes,
Pythium ultimum
and
Phytophthora sojae
, their growth was inhibited, and their ability to infect plants was diminished. Specifically, PuPuf4 binds to the H68 component of 25S rRNA and regulates the degradation of rRNA maturation byproducts. Additionally, we discovered a novel AG-rich motif that serves as a binding site for L-shaped PUF proteins. Furthermore, we developed a nano-material-free dsRNA delivery system targeting
Puf4
, which effectively reduced the virulence of
Pythium
and
Phytophthora
pathogens. Our findings not only uncover a fundamental process in oomycetes but also provide a sustainable approach to protect crops from these destructive microbes. Ribosome biogenesis is an essential and tightly regulated process linked to cell proliferation and growth. However, its regulatory mechanisms in oomycetes, a group of organisms with significant agricultural and ecological importance, remain unclear. In this study, we identify Puf4, a non-classical PUF (Pumilio and FBF) family RNA-binding protein that plays a conserved and crucial role in pre-rRNA processing in oomycetes. Knockout of PuPuf4 in Pythium ultimum or its ortholog PsPuf4 in Phytophthora sojae results in defective vegetative growth, impaired development, and reduced pathogenicity. Specifically, PuPuf4 binds to the H68 component of 25S rRNA, and its knockout leads to overaccumulation of rRNA processing intermediates, including 5'ETS, ITS1, and ITS2 precursors. Additionally, the AG-rich motif identified as the first binding motif of L-shaped PUF proteins, including PuPuf4, APUM24, and ScPuf6, may contribute to their specific RNA-binding affinity due to its unique structural features. Given the conserved role of Puf4 in oomycete pathogenicity, we developed the first nano-material-free dsRNA delivery system via zoospore-specific uptake, effectively attenuating virulence in Pythium aphanidermatum and Ph. sojae through RNAi targeting Puf4. This study presents novel findings on structural and functional conservation of Puf4 and offers a promising RNAi-based strategy for controlling oomycete plant diseases.Ribosome biogenesis is an essential and tightly regulated process linked to cell proliferation and growth. However, its regulatory mechanisms in oomycetes, a group of organisms with significant agricultural and ecological importance, remain unclear. In this study, we identify Puf4, a non-classical PUF (Pumilio and FBF) family RNA-binding protein that plays a conserved and crucial role in pre-rRNA processing in oomycetes. Knockout of PuPuf4 in Pythium ultimum or its ortholog PsPuf4 in Phytophthora sojae results in defective vegetative growth, impaired development, and reduced pathogenicity. Specifically, PuPuf4 binds to the H68 component of 25S rRNA, and its knockout leads to overaccumulation of rRNA processing intermediates, including 5'ETS, ITS1, and ITS2 precursors. Additionally, the AG-rich motif identified as the first binding motif of L-shaped PUF proteins, including PuPuf4, APUM24, and ScPuf6, may contribute to their specific RNA-binding affinity due to its unique structural features. Given the conserved role of Puf4 in oomycete pathogenicity, we developed the first nano-material-free dsRNA delivery system via zoospore-specific uptake, effectively attenuating virulence in Pythium aphanidermatum and Ph. sojae through RNAi targeting Puf4. This study presents novel findings on structural and functional conservation of Puf4 and offers a promising RNAi-based strategy for controlling oomycete plant diseases. Ribosome biogenesis is an essential and tightly regulated process linked to cell proliferation and growth. However, its regulatory mechanisms in oomycetes, a group of organisms with significant agricultural and ecological importance, remain unclear. In this study, we identify Puf4, a non-classical PUF (Pumilio and FBF) family RNA-binding protein that plays a conserved and crucial role in pre-rRNA processing in oomycetes. Knockout of PuPuf4 in Pythium ultimum or its ortholog PsPuf4 in Phytophthora sojae results in defective vegetative growth, impaired development, and reduced pathogenicity. Specifically, PuPuf4 binds to the H68 component of 25S rRNA, and its knockout leads to overaccumulation of rRNA processing intermediates, including 5′ETS, ITS1, and ITS2 precursors. Additionally, the AG-rich motif identified as the first binding motif of L-shaped PUF proteins, including PuPuf4, APUM24, and ScPuf6, may contribute to their specific RNA-binding affinity due to its unique structural features. Given the conserved role of Puf4 in oomycete pathogenicity, we developed the first nano-material-free dsRNA delivery system via zoospore-specific uptake, effectively attenuating virulence in Pythium aphanidermatum and Ph. sojae through RNAi targeting Puf4 . This study presents novel findings on structural and functional conservation of Puf4 and offers a promising RNAi-based strategy for controlling oomycete plant diseases. |
Author | Zhang, Zhichao Wan, Chuanxu Ye, Wenwu Zheng, Xiaobo Feng, Hui Liu, Tianli Wang, Yuanchao Wang, Jie |
AuthorAffiliation | 1 Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao, Shandong, China University of Cambridge, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND 3 Key Laboratory of Soybean Disease and Pest Control (Ministry of Agriculture and Rural Affairs), Nanjing Agricultural University, Nanjing, Jiangsu, China 2 Department of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu, China |
AuthorAffiliation_xml | – name: University of Cambridge, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND – name: 2 Department of Plant Pathology, Nanjing Agricultural University, Nanjing, Jiangsu, China – name: 1 Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao, Shandong, China – name: 3 Key Laboratory of Soybean Disease and Pest Control (Ministry of Agriculture and Rural Affairs), Nanjing Agricultural University, Nanjing, Jiangsu, China |
Author_xml | – sequence: 1 givenname: Hui surname: Feng fullname: Feng, Hui – sequence: 2 givenname: Tianli surname: Liu fullname: Liu, Tianli – sequence: 3 givenname: Chuanxu surname: Wan fullname: Wan, Chuanxu – sequence: 4 givenname: Zhichao surname: Zhang fullname: Zhang, Zhichao – sequence: 5 givenname: Yuanchao surname: Wang fullname: Wang, Yuanchao – sequence: 6 givenname: Xiaobo surname: Zheng fullname: Zheng, Xiaobo – sequence: 7 givenname: Jie surname: Wang fullname: Wang, Jie – sequence: 8 givenname: Wenwu orcidid: 0000-0001-7347-8935 surname: Ye fullname: Ye, Wenwu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40743283$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1146/annurev-arplant-050213-040159 10.1126/science.1212642 10.1038/nprot.2006.47 10.1038/s41467-023-41447-8 10.3390/biom11101475 10.1371/journal.ppat.1010001 10.1016/j.tplants.2009.06.009 10.1038/s41586-023-05767-5 10.1111/mpp.12318 10.1038/s41467-023-36867-5 10.1186/s42483-023-00189-7 10.1371/journal.ppat.1008967 10.1016/j.cell.2017.11.039 10.1093/emboj/20.22.6475 10.1105/tpc.17.00778 10.1016/j.fgb.2016.12.002 10.1111/mpp.12190 10.1016/j.ab.2016.07.027 10.1094/PHYTO-02-21-0054-SC 10.1186/s12915-020-00814-3 10.1007/s10658-020-02076-9 10.1007/978-1-4939-3067-8_9 10.1111/j.1365-313X.2010.04393.x 10.1111/pbi.13589 10.1093/jxb/ert478 10.1016/j.copbio.2021.06.005 10.1093/nar/gkad794 10.1002/wrna.69 10.1126/science.1241911 10.1016/j.gde.2019.07.019 10.1016/j.plantsci.2020.110505 10.1093/nar/gky803 10.1002/adfm.202213143 10.1016/j.tplants.2015.07.003 10.1128/EC.00286-08 10.1007/s00709-011-0269-2 10.1038/s41467-021-24964-2 10.1186/1471-2229-10-44 10.1073/pnas.1407634112 10.1016/j.tim.2016.11.011 10.1128/EC.00091-08 10.15252/embr.202356910 10.1080/07060661.2014.920921 10.1146/annurev.cellbio.042308.113417 10.1111/ppa.13187 |
ContentType | Journal Article |
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SubjectTerms | Biology and Life Sciences Oomycetes - genetics Oomycetes - metabolism Oomycetes - pathogenicity Phytophthora - genetics Phytophthora - metabolism Phytophthora - pathogenicity Plant Diseases - microbiology Plant Diseases - prevention & control Pythium - genetics Pythium - metabolism Pythium - pathogenicity Research and Analysis Methods RNA Interference RNA Precursors - genetics RNA Precursors - metabolism RNA Processing, Post-Transcriptional RNA-Binding Proteins - genetics RNA-Binding Proteins - metabolism |
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Title | A non-classical PUF family protein in oomycetes functions as a pre-rRNA processing regulator and a target for RNAi-based disease control |
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