Cargando…

S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination

Geminiviruses, such as beet severe curly top virus (BSCTV), are a group of DNA viruses that cause severe plant diseases and agricultural losses. The C4 protein is a major symptom determinant in several geminiviruses; however, its regulatory mechanism and molecular function in plant cells remain uncl...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Huiyun, Zeng, Runxiu, Chen, Zian, Liu, Xiaoshi, Cao, Zhendan, Xie, Qi, Yang, Chengwei, Lai, Jianbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093331/
https://www.ncbi.nlm.nih.gov/pubmed/29931348
http://dx.doi.org/10.1093/jxb/ery228
_version_ 1783347676455108608
author Li, Huiyun
Zeng, Runxiu
Chen, Zian
Liu, Xiaoshi
Cao, Zhendan
Xie, Qi
Yang, Chengwei
Lai, Jianbin
author_facet Li, Huiyun
Zeng, Runxiu
Chen, Zian
Liu, Xiaoshi
Cao, Zhendan
Xie, Qi
Yang, Chengwei
Lai, Jianbin
author_sort Li, Huiyun
collection PubMed
description Geminiviruses, such as beet severe curly top virus (BSCTV), are a group of DNA viruses that cause severe plant diseases and agricultural losses. The C4 protein is a major symptom determinant in several geminiviruses; however, its regulatory mechanism and molecular function in plant cells remain unclear. Here, we show that BSCTV C4 is S-acylated in planta, and that this post-translational lipid modification is necessary for its membrane localization and functions, especially its regulation of shoot development of host plants. Furthermore, the S-acylated form of C4 interacts with CLAVATA 1 (CLV1), an important receptor kinase in meristem maintenance, and consequentially affects the expression of WUSCHEL, a major target of CLV1. The abnormal development of siliques in Arabidopsis thaliana infected with BSCTV is also dependent on the S-acylation of C4, implying a potential role of CLAVATA signaling in this process. Collectively, our results show that S-acylation is essential for BSCTV C4 function, including the regulation of the CLAVATA pathway, during geminivirus infection.
format Online
Article
Text
id pubmed-6093331
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-60933312018-08-22 S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination Li, Huiyun Zeng, Runxiu Chen, Zian Liu, Xiaoshi Cao, Zhendan Xie, Qi Yang, Chengwei Lai, Jianbin J Exp Bot Research Papers Geminiviruses, such as beet severe curly top virus (BSCTV), are a group of DNA viruses that cause severe plant diseases and agricultural losses. The C4 protein is a major symptom determinant in several geminiviruses; however, its regulatory mechanism and molecular function in plant cells remain unclear. Here, we show that BSCTV C4 is S-acylated in planta, and that this post-translational lipid modification is necessary for its membrane localization and functions, especially its regulation of shoot development of host plants. Furthermore, the S-acylated form of C4 interacts with CLAVATA 1 (CLV1), an important receptor kinase in meristem maintenance, and consequentially affects the expression of WUSCHEL, a major target of CLV1. The abnormal development of siliques in Arabidopsis thaliana infected with BSCTV is also dependent on the S-acylation of C4, implying a potential role of CLAVATA signaling in this process. Collectively, our results show that S-acylation is essential for BSCTV C4 function, including the regulation of the CLAVATA pathway, during geminivirus infection. Oxford University Press 2018-08-17 2018-06-20 /pmc/articles/PMC6093331/ /pubmed/29931348 http://dx.doi.org/10.1093/jxb/ery228 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Li, Huiyun
Zeng, Runxiu
Chen, Zian
Liu, Xiaoshi
Cao, Zhendan
Xie, Qi
Yang, Chengwei
Lai, Jianbin
S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination
title S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination
title_full S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination
title_fullStr S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination
title_full_unstemmed S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination
title_short S-acylation of a geminivirus C4 protein is essential for regulating the CLAVATA pathway in symptom determination
title_sort s-acylation of a geminivirus c4 protein is essential for regulating the clavata pathway in symptom determination
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093331/
https://www.ncbi.nlm.nih.gov/pubmed/29931348
http://dx.doi.org/10.1093/jxb/ery228
work_keys_str_mv AT lihuiyun sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT zengrunxiu sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT chenzian sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT liuxiaoshi sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT caozhendan sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT xieqi sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT yangchengwei sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination
AT laijianbin sacylationofageminivirusc4proteinisessentialforregulatingtheclavatapathwayinsymptomdetermination