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Unraveling the role of MADS transcription factor complexes in apple tree dormancy

A group of MADS transcription factors (TFs) are believed to control temperature‐mediated bud dormancy. These TFs, called DORMANCY‐ASSOCIATED MADS‐BOX (DAM), are encoded by genes similar to SHORT VEGETATIVE PHASE (SVP) from Arabidopsis. MADS proteins form transcriptional complexes whose combinatory c...

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Autores principales: da Silveira Falavigna, Vítor, Severing, Edouard, Lai, Xuelei, Estevan, Joan, Farrera, Isabelle, Hugouvieux, Véronique, Revers, Luís Fernando, Zubieta, Chloe, Coupland, George, Costes, Evelyne, Andrés, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292984/
https://www.ncbi.nlm.nih.gov/pubmed/34480759
http://dx.doi.org/10.1111/nph.17710
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author da Silveira Falavigna, Vítor
Severing, Edouard
Lai, Xuelei
Estevan, Joan
Farrera, Isabelle
Hugouvieux, Véronique
Revers, Luís Fernando
Zubieta, Chloe
Coupland, George
Costes, Evelyne
Andrés, Fernando
author_facet da Silveira Falavigna, Vítor
Severing, Edouard
Lai, Xuelei
Estevan, Joan
Farrera, Isabelle
Hugouvieux, Véronique
Revers, Luís Fernando
Zubieta, Chloe
Coupland, George
Costes, Evelyne
Andrés, Fernando
author_sort da Silveira Falavigna, Vítor
collection PubMed
description A group of MADS transcription factors (TFs) are believed to control temperature‐mediated bud dormancy. These TFs, called DORMANCY‐ASSOCIATED MADS‐BOX (DAM), are encoded by genes similar to SHORT VEGETATIVE PHASE (SVP) from Arabidopsis. MADS proteins form transcriptional complexes whose combinatory composition defines their molecular function. However, how MADS multimeric complexes control the dormancy cycle in trees is unclear. Apple MdDAM and other dormancy‐related MADS proteins form complexes with MdSVPa, which is essential for the ability of transcriptional complexes to bind to DNA. Sequential DNA‐affinity purification sequencing (seq‐DAP‐seq) was performed to identify the genome‐wide binding sites of apple MADS TF complexes. Target genes associated with the binding sites were identified by combining seq‐DAP‐seq data with transcriptomics datasets obtained using a glucocorticoid receptor fusion system, and RNA‐seq data related to apple dormancy. We describe a gene regulatory network (GRN) formed by MdSVPa‐containing complexes, which regulate the dormancy cycle in response to environmental cues and hormonal signaling pathways. Additionally, novel molecular evidence regarding the evolutionary functional segregation between DAM and SVP proteins in the Rosaceae is presented. MdSVPa sequentially forms complexes with the MADS TFs that predominate at each dormancy phase, altering its DNA‐binding specificity and, therefore, the transcriptional regulation of its target genes.
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spelling pubmed-92929842022-07-20 Unraveling the role of MADS transcription factor complexes in apple tree dormancy da Silveira Falavigna, Vítor Severing, Edouard Lai, Xuelei Estevan, Joan Farrera, Isabelle Hugouvieux, Véronique Revers, Luís Fernando Zubieta, Chloe Coupland, George Costes, Evelyne Andrés, Fernando New Phytol Research A group of MADS transcription factors (TFs) are believed to control temperature‐mediated bud dormancy. These TFs, called DORMANCY‐ASSOCIATED MADS‐BOX (DAM), are encoded by genes similar to SHORT VEGETATIVE PHASE (SVP) from Arabidopsis. MADS proteins form transcriptional complexes whose combinatory composition defines their molecular function. However, how MADS multimeric complexes control the dormancy cycle in trees is unclear. Apple MdDAM and other dormancy‐related MADS proteins form complexes with MdSVPa, which is essential for the ability of transcriptional complexes to bind to DNA. Sequential DNA‐affinity purification sequencing (seq‐DAP‐seq) was performed to identify the genome‐wide binding sites of apple MADS TF complexes. Target genes associated with the binding sites were identified by combining seq‐DAP‐seq data with transcriptomics datasets obtained using a glucocorticoid receptor fusion system, and RNA‐seq data related to apple dormancy. We describe a gene regulatory network (GRN) formed by MdSVPa‐containing complexes, which regulate the dormancy cycle in response to environmental cues and hormonal signaling pathways. Additionally, novel molecular evidence regarding the evolutionary functional segregation between DAM and SVP proteins in the Rosaceae is presented. MdSVPa sequentially forms complexes with the MADS TFs that predominate at each dormancy phase, altering its DNA‐binding specificity and, therefore, the transcriptional regulation of its target genes. John Wiley and Sons Inc. 2021-09-23 2021-12 /pmc/articles/PMC9292984/ /pubmed/34480759 http://dx.doi.org/10.1111/nph.17710 Text en © 2021 The Authors. New Phytologist © 2021 New Phytologist Foundation https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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
da Silveira Falavigna, Vítor
Severing, Edouard
Lai, Xuelei
Estevan, Joan
Farrera, Isabelle
Hugouvieux, Véronique
Revers, Luís Fernando
Zubieta, Chloe
Coupland, George
Costes, Evelyne
Andrés, Fernando
Unraveling the role of MADS transcription factor complexes in apple tree dormancy
title Unraveling the role of MADS transcription factor complexes in apple tree dormancy
title_full Unraveling the role of MADS transcription factor complexes in apple tree dormancy
title_fullStr Unraveling the role of MADS transcription factor complexes in apple tree dormancy
title_full_unstemmed Unraveling the role of MADS transcription factor complexes in apple tree dormancy
title_short Unraveling the role of MADS transcription factor complexes in apple tree dormancy
title_sort unraveling the role of mads transcription factor complexes in apple tree dormancy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292984/
https://www.ncbi.nlm.nih.gov/pubmed/34480759
http://dx.doi.org/10.1111/nph.17710
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