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Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice

SCF (Skp1/Cullin1/F‐box) complexes are key regulators of many cellular processes. Viruses encode specific factors to interfere with or hijack these complexes and ensure their infection in plants. The molecular mechanisms controlling this interference/hijack are currently largely unknown. Here, we pr...

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Autores principales: He, Long, Chen, Xuan, Yang, Jin, Zhang, Tianye, Li, Juan, Zhang, Songbai, Zhong, Kaili, Zhang, Hengmu, Chen, Jianping, Yang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972624/
https://www.ncbi.nlm.nih.gov/pubmed/31318448
http://dx.doi.org/10.1111/nph.16066
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author He, Long
Chen, Xuan
Yang, Jin
Zhang, Tianye
Li, Juan
Zhang, Songbai
Zhong, Kaili
Zhang, Hengmu
Chen, Jianping
Yang, Jian
author_facet He, Long
Chen, Xuan
Yang, Jin
Zhang, Tianye
Li, Juan
Zhang, Songbai
Zhong, Kaili
Zhang, Hengmu
Chen, Jianping
Yang, Jian
author_sort He, Long
collection PubMed
description SCF (Skp1/Cullin1/F‐box) complexes are key regulators of many cellular processes. Viruses encode specific factors to interfere with or hijack these complexes and ensure their infection in plants. The molecular mechanisms controlling this interference/hijack are currently largely unknown. Here, we present evidence of a novel strategy used by Rice black‐streaked dwarf virus (RBSDV) to regulate ubiquitination in rice (Oryza sativa) by interfering in the activity of OsCSN5A. We also show that RBSDV P5‐1 specifically affects CSN‐mediated deRUBylation of OsCUL1, compromising the integrity of the SCF(COI1) complex. We demonstrate that the expressions of jasmonate (JA) biosynthesis‐associated genes are not inhibited, whereas the expressions of JA‐responsive genes are down‐regulated in transgenic P5‐1 plants. More importantly, application of JA to P5‐1 transgenic plants did not reduce their susceptibility to RBSDV infection. Our results suggest that P5‐1 inhibits the ubiquitination activity of SCF E3 ligases through an interaction with OsCSN5A, and hinders the RUBylation/deRUBylation of CUL1, leading to an inhibition of the JA response pathway and an enhancement of RBSDV infection in rice.
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spelling pubmed-69726242020-01-27 Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice He, Long Chen, Xuan Yang, Jin Zhang, Tianye Li, Juan Zhang, Songbai Zhong, Kaili Zhang, Hengmu Chen, Jianping Yang, Jian New Phytol Research SCF (Skp1/Cullin1/F‐box) complexes are key regulators of many cellular processes. Viruses encode specific factors to interfere with or hijack these complexes and ensure their infection in plants. The molecular mechanisms controlling this interference/hijack are currently largely unknown. Here, we present evidence of a novel strategy used by Rice black‐streaked dwarf virus (RBSDV) to regulate ubiquitination in rice (Oryza sativa) by interfering in the activity of OsCSN5A. We also show that RBSDV P5‐1 specifically affects CSN‐mediated deRUBylation of OsCUL1, compromising the integrity of the SCF(COI1) complex. We demonstrate that the expressions of jasmonate (JA) biosynthesis‐associated genes are not inhibited, whereas the expressions of JA‐responsive genes are down‐regulated in transgenic P5‐1 plants. More importantly, application of JA to P5‐1 transgenic plants did not reduce their susceptibility to RBSDV infection. Our results suggest that P5‐1 inhibits the ubiquitination activity of SCF E3 ligases through an interaction with OsCSN5A, and hinders the RUBylation/deRUBylation of CUL1, leading to an inhibition of the JA response pathway and an enhancement of RBSDV infection in rice. John Wiley and Sons Inc. 2019-08-09 2020-01 /pmc/articles/PMC6972624/ /pubmed/31318448 http://dx.doi.org/10.1111/nph.16066 Text en © 2019 The Authors. New Phytologist © 2019 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
He, Long
Chen, Xuan
Yang, Jin
Zhang, Tianye
Li, Juan
Zhang, Songbai
Zhong, Kaili
Zhang, Hengmu
Chen, Jianping
Yang, Jian
Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice
title Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice
title_full Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice
title_fullStr Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice
title_full_unstemmed Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice
title_short Rice black‐streaked dwarf virus‐encoded P5‐1 regulates the ubiquitination activity of SCF E3 ligases and inhibits jasmonate signaling to benefit its infection in rice
title_sort rice black‐streaked dwarf virus‐encoded p5‐1 regulates the ubiquitination activity of scf e3 ligases and inhibits jasmonate signaling to benefit its infection in rice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972624/
https://www.ncbi.nlm.nih.gov/pubmed/31318448
http://dx.doi.org/10.1111/nph.16066
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