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Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance

Poly(A) tail shortening is a critical step in messenger RNA (mRNA) decay and control of gene expression. The carbon catabolite repressor 4 (CCR4)‐associated factor 1 (CAF1) component of the CCR4‐NOT deadenylase complex plays an essential role in mRNA deadenylation in most eukaryotes. However, while...

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Autores principales: Shimo, Hugo Massayoshi, Terassi, Carolina, Lima Silva, Caio Cesar, Zanella, Jackeline de Lima, Mercaldi, Gustavo Fernando, Rocco, Silvana Aparecida, Benedetti, Celso Eduardo
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/PMC6640180/
https://www.ncbi.nlm.nih.gov/pubmed/31115151
http://dx.doi.org/10.1111/mpp.12815
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author Shimo, Hugo Massayoshi
Terassi, Carolina
Lima Silva, Caio Cesar
Zanella, Jackeline de Lima
Mercaldi, Gustavo Fernando
Rocco, Silvana Aparecida
Benedetti, Celso Eduardo
author_facet Shimo, Hugo Massayoshi
Terassi, Carolina
Lima Silva, Caio Cesar
Zanella, Jackeline de Lima
Mercaldi, Gustavo Fernando
Rocco, Silvana Aparecida
Benedetti, Celso Eduardo
author_sort Shimo, Hugo Massayoshi
collection PubMed
description Poly(A) tail shortening is a critical step in messenger RNA (mRNA) decay and control of gene expression. The carbon catabolite repressor 4 (CCR4)‐associated factor 1 (CAF1) component of the CCR4‐NOT deadenylase complex plays an essential role in mRNA deadenylation in most eukaryotes. However, while CAF1 has been extensively investigated in yeast and animals, its role in plants remains largely unknown. Here, we show that the Citrus sinensis CAF1 (CsCAF1) is a magnesium‐dependent deadenylase implicated in resistance against the citrus canker bacteria Xanthomonas citri. CsCAF1 interacted with proteins of the CCR4‐NOT complex, including CsVIP2, a NOT2 homologue, translin‐associated factor X (CsTRAX) and the poly(A)‐binding proteins CsPABPN and CsPABPC. CsCAF1 also interacted with PthA4, the main X. citri effector required for citrus canker elicitation. We also present evidence suggesting that PthA4 inhibits CsCAF1 deadenylase activity in vitro and stabilizes the mRNA encoded by the citrus canker susceptibility gene CsLOB1, which is transcriptionally activated by PthA4 during canker formation. Moreover, we show that an inhibitor of CsCAF1 deadenylase activity significantly enhanced canker development, despite causing a reduction in PthA4‐dependent CsLOB1 transcription. These results thus link CsCAF1 with canker development and PthA4‐dependent transcription in citrus plants.
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spelling pubmed-66401802019-09-16 Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance Shimo, Hugo Massayoshi Terassi, Carolina Lima Silva, Caio Cesar Zanella, Jackeline de Lima Mercaldi, Gustavo Fernando Rocco, Silvana Aparecida Benedetti, Celso Eduardo Mol Plant Pathol Original Articles Poly(A) tail shortening is a critical step in messenger RNA (mRNA) decay and control of gene expression. The carbon catabolite repressor 4 (CCR4)‐associated factor 1 (CAF1) component of the CCR4‐NOT deadenylase complex plays an essential role in mRNA deadenylation in most eukaryotes. However, while CAF1 has been extensively investigated in yeast and animals, its role in plants remains largely unknown. Here, we show that the Citrus sinensis CAF1 (CsCAF1) is a magnesium‐dependent deadenylase implicated in resistance against the citrus canker bacteria Xanthomonas citri. CsCAF1 interacted with proteins of the CCR4‐NOT complex, including CsVIP2, a NOT2 homologue, translin‐associated factor X (CsTRAX) and the poly(A)‐binding proteins CsPABPN and CsPABPC. CsCAF1 also interacted with PthA4, the main X. citri effector required for citrus canker elicitation. We also present evidence suggesting that PthA4 inhibits CsCAF1 deadenylase activity in vitro and stabilizes the mRNA encoded by the citrus canker susceptibility gene CsLOB1, which is transcriptionally activated by PthA4 during canker formation. Moreover, we show that an inhibitor of CsCAF1 deadenylase activity significantly enhanced canker development, despite causing a reduction in PthA4‐dependent CsLOB1 transcription. These results thus link CsCAF1 with canker development and PthA4‐dependent transcription in citrus plants. John Wiley and Sons Inc. 2019-05-21 /pmc/articles/PMC6640180/ /pubmed/31115151 http://dx.doi.org/10.1111/mpp.12815 Text en © 2019 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd 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 Original Articles
Shimo, Hugo Massayoshi
Terassi, Carolina
Lima Silva, Caio Cesar
Zanella, Jackeline de Lima
Mercaldi, Gustavo Fernando
Rocco, Silvana Aparecida
Benedetti, Celso Eduardo
Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance
title Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance
title_full Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance
title_fullStr Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance
title_full_unstemmed Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance
title_short Role of the Citrus sinensis RNA deadenylase CsCAF1 in citrus canker resistance
title_sort role of the citrus sinensis rna deadenylase cscaf1 in citrus canker resistance
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6640180/
https://www.ncbi.nlm.nih.gov/pubmed/31115151
http://dx.doi.org/10.1111/mpp.12815
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