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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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. |
format | Online Article Text |
id | pubmed-6640180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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