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Inhibition of Arabidopsis thaliana CIN‐like TCP transcription factors by Agrobacterium T‐DNA‐encoded 6B proteins

Summary Agrobacterium T‐DNA‐encoded 6B proteins cause remarkable growth effects in plants. Nicotiana otophora carries two cellular T‐DNAs with three slightly divergent 6b genes (TE‐1‐6b‐L, TE‐1‐6b‐R and TE‐2‐6b) originating from a natural transformation event. In Arabidopsis thaliana, expression of...

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Published in:The Plant journal : for cell and molecular biology 2020-03, Vol.101 (6), p.1303-1317
Main Authors: Potuschak, Thomas, Palatnik, Javier, Schommer, Carla, Sierro, Nicolas, Ivanov, Nikolai V., Kwon, Yerim, Genschik, Pascal, Davière, Jean‐Michel, Otten, Léon
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container_title The Plant journal : for cell and molecular biology
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creator Potuschak, Thomas
Palatnik, Javier
Schommer, Carla
Sierro, Nicolas
Ivanov, Nikolai V.
Kwon, Yerim
Genschik, Pascal
Davière, Jean‐Michel
Otten, Léon
description Summary Agrobacterium T‐DNA‐encoded 6B proteins cause remarkable growth effects in plants. Nicotiana otophora carries two cellular T‐DNAs with three slightly divergent 6b genes (TE‐1‐6b‐L, TE‐1‐6b‐R and TE‐2‐6b) originating from a natural transformation event. In Arabidopsis thaliana, expression of 2×35S:TE‐2‐6b, but not 2×35S:TE‐1‐6b‐L or 2×35S:TE‐1‐6b‐R, led to plants with crinkly leaves, which strongly resembled mutants of the miR319a/TCP module. This module is composed of MIR319A and five CIN‐like TCP (TEOSINTHE BRANCHED1, CYCLOIDEA and PROLIFERATING CELL NUCLEAR ANTIGEN BINDING FACTOR) genes (TCP2, TCP3, TCP4, TCP10 and TCP24) targeted by miR319a. The CIN‐like TCP genes encode transcription factors and are required for cell division arrest at leaf margins during development. MIR319A overexpression causes excessive growth and crinkly leaves. TE‐2‐6b plants did not show increased miR319a levels, but the mRNA levels of the TCP4 target gene LOX2 were decreased, as in jaw‐D plants. Co‐expression of green fluorescent protein (GFP)‐tagged TCPs with native or red fluorescent protein (RFP)‐tagged TE‐6B proteins led to an increase in TCP protein levels and formation of numerous cytoplasmic dots containing 6B and TCP proteins. Yeast double‐hybrid experiments confirmed 6B/TCP binding and showed that TE‐1‐6B‐L and TE‐1‐6B‐R bind a smaller set of TCP proteins than TE‐2‐6B. A single nucleotide mutation in TE‐1‐6B‐R enlarged its TCP‐binding repertoire to that of TE‐2‐6B and caused a crinkly phenotype in Arabidopsis. Deletion analysis showed that TE‐2‐6B targets the TCP4 DNA‐binding domain and directly interferes with transcriptional activation. Taken together, these results provide detailed insights into the mechanism of action of the N. otophora TE‐encoded 6b genes. Significance Statement It was found previously that the Agrobacterium‐derived TE‐2‐6b gene from Nicotiana otophora induces strong growth effects in Nicotiana tabacum. However, the molecular mechanism has remained unknown. We show here that TE‐2‐6b induces a jaw‐D‐like phenotype in Arabidopsis – known to result from a decrease in CIN‐like TCPs – and that different TE‐6B proteins interact with different TCP subsets, thus providing insights into the molecular mechanism by which TE‐6B proteins stimulate plant growth.
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Nicotiana otophora carries two cellular T‐DNAs with three slightly divergent 6b genes (TE‐1‐6b‐L, TE‐1‐6b‐R and TE‐2‐6b) originating from a natural transformation event. In Arabidopsis thaliana, expression of 2×35S:TE‐2‐6b, but not 2×35S:TE‐1‐6b‐L or 2×35S:TE‐1‐6b‐R, led to plants with crinkly leaves, which strongly resembled mutants of the miR319a/TCP module. This module is composed of MIR319A and five CIN‐like TCP (TEOSINTHE BRANCHED1, CYCLOIDEA and PROLIFERATING CELL NUCLEAR ANTIGEN BINDING FACTOR) genes (TCP2, TCP3, TCP4, TCP10 and TCP24) targeted by miR319a. The CIN‐like TCP genes encode transcription factors and are required for cell division arrest at leaf margins during development. MIR319A overexpression causes excessive growth and crinkly leaves. TE‐2‐6b plants did not show increased miR319a levels, but the mRNA levels of the TCP4 target gene LOX2 were decreased, as in jaw‐D plants. Co‐expression of green fluorescent protein (GFP)‐tagged TCPs with native or red fluorescent protein (RFP)‐tagged TE‐6B proteins led to an increase in TCP protein levels and formation of numerous cytoplasmic dots containing 6B and TCP proteins. Yeast double‐hybrid experiments confirmed 6B/TCP binding and showed that TE‐1‐6B‐L and TE‐1‐6B‐R bind a smaller set of TCP proteins than TE‐2‐6B. A single nucleotide mutation in TE‐1‐6B‐R enlarged its TCP‐binding repertoire to that of TE‐2‐6B and caused a crinkly phenotype in Arabidopsis. Deletion analysis showed that TE‐2‐6B targets the TCP4 DNA‐binding domain and directly interferes with transcriptional activation. Taken together, these results provide detailed insights into the mechanism of action of the N. otophora TE‐encoded 6b genes. Significance Statement It was found previously that the Agrobacterium‐derived TE‐2‐6b gene from Nicotiana otophora induces strong growth effects in Nicotiana tabacum. However, the molecular mechanism has remained unknown. We show here that TE‐2‐6b induces a jaw‐D‐like phenotype in Arabidopsis – known to result from a decrease in CIN‐like TCPs – and that different TE‐6B proteins interact with different TCP subsets, thus providing insights into the molecular mechanism by which TE‐6B proteins stimulate plant growth.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.14591</identifier><identifier>PMID: 31659801</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>6b oncogene ; Agrobacterium ; Agrobacterium - metabolism ; Antigens ; Arabidopsis - metabolism ; Arabidopsis - microbiology ; Arabidopsis Proteins - antagonists &amp; inhibitors ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Bacterial Proteins - metabolism ; Binding ; Cell division ; Deoxyribonucleic acid ; DNA ; DNA, Bacterial - metabolism ; Fluorescence ; Gene expression ; Gene Expression Profiling ; Genes ; Genetic transformation ; Green fluorescent protein ; Jaw ; jaw‐D phenotype ; Leaves ; Microscopy, Confocal ; Modules ; Mutants ; Mutation ; natural transformant ; Nicotiana - metabolism ; Nicotiana - microbiology ; Nicotiana otophora ; Nucleotides ; Original ; Phenotypes ; Plant Diseases - microbiology ; Plant Leaves - metabolism ; Plant Leaves - microbiology ; Plants ; Polymerase Chain Reaction ; Proliferating cell nuclear antigen ; Proteins ; Red fluorescent protein ; TCP genes ; Transcription activation ; Transcription factors ; Transcription Factors - antagonists &amp; inhibitors ; Two-Hybrid System Techniques ; Yeasts</subject><ispartof>The Plant journal : for cell and molecular biology, 2020-03, Vol.101 (6), p.1303-1317</ispartof><rights>2019 The Authors published by Society for Experimental Biology and John Wiley &amp; Sons Ltd</rights><rights>2019 The Authors The Plant Journal published by Society for Experimental Biology and John Wiley &amp; Sons Ltd.</rights><rights>2019. 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Nicotiana otophora carries two cellular T‐DNAs with three slightly divergent 6b genes (TE‐1‐6b‐L, TE‐1‐6b‐R and TE‐2‐6b) originating from a natural transformation event. In Arabidopsis thaliana, expression of 2×35S:TE‐2‐6b, but not 2×35S:TE‐1‐6b‐L or 2×35S:TE‐1‐6b‐R, led to plants with crinkly leaves, which strongly resembled mutants of the miR319a/TCP module. This module is composed of MIR319A and five CIN‐like TCP (TEOSINTHE BRANCHED1, CYCLOIDEA and PROLIFERATING CELL NUCLEAR ANTIGEN BINDING FACTOR) genes (TCP2, TCP3, TCP4, TCP10 and TCP24) targeted by miR319a. The CIN‐like TCP genes encode transcription factors and are required for cell division arrest at leaf margins during development. MIR319A overexpression causes excessive growth and crinkly leaves. TE‐2‐6b plants did not show increased miR319a levels, but the mRNA levels of the TCP4 target gene LOX2 were decreased, as in jaw‐D plants. Co‐expression of green fluorescent protein (GFP)‐tagged TCPs with native or red fluorescent protein (RFP)‐tagged TE‐6B proteins led to an increase in TCP protein levels and formation of numerous cytoplasmic dots containing 6B and TCP proteins. Yeast double‐hybrid experiments confirmed 6B/TCP binding and showed that TE‐1‐6B‐L and TE‐1‐6B‐R bind a smaller set of TCP proteins than TE‐2‐6B. A single nucleotide mutation in TE‐1‐6B‐R enlarged its TCP‐binding repertoire to that of TE‐2‐6B and caused a crinkly phenotype in Arabidopsis. Deletion analysis showed that TE‐2‐6B targets the TCP4 DNA‐binding domain and directly interferes with transcriptional activation. Taken together, these results provide detailed insights into the mechanism of action of the N. otophora TE‐encoded 6b genes. Significance Statement It was found previously that the Agrobacterium‐derived TE‐2‐6b gene from Nicotiana otophora induces strong growth effects in Nicotiana tabacum. However, the molecular mechanism has remained unknown. We show here that TE‐2‐6b induces a jaw‐D‐like phenotype in Arabidopsis – known to result from a decrease in CIN‐like TCPs – and that different TE‐6B proteins interact with different TCP subsets, thus providing insights into the molecular mechanism by which TE‐6B proteins stimulate plant growth.</description><subject>6b oncogene</subject><subject>Agrobacterium</subject><subject>Agrobacterium - metabolism</subject><subject>Antigens</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis - microbiology</subject><subject>Arabidopsis Proteins - antagonists &amp; inhibitors</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Bacterial Proteins - metabolism</subject><subject>Binding</subject><subject>Cell division</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Bacterial - metabolism</subject><subject>Fluorescence</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Genes</subject><subject>Genetic transformation</subject><subject>Green fluorescent protein</subject><subject>Jaw</subject><subject>jaw‐D phenotype</subject><subject>Leaves</subject><subject>Microscopy, Confocal</subject><subject>Modules</subject><subject>Mutants</subject><subject>Mutation</subject><subject>natural transformant</subject><subject>Nicotiana - metabolism</subject><subject>Nicotiana - microbiology</subject><subject>Nicotiana otophora</subject><subject>Nucleotides</subject><subject>Original</subject><subject>Phenotypes</subject><subject>Plant Diseases - microbiology</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Leaves - microbiology</subject><subject>Plants</subject><subject>Polymerase Chain Reaction</subject><subject>Proliferating cell nuclear antigen</subject><subject>Proteins</subject><subject>Red fluorescent protein</subject><subject>TCP genes</subject><subject>Transcription activation</subject><subject>Transcription factors</subject><subject>Transcription Factors - antagonists &amp; 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Nicotiana otophora carries two cellular T‐DNAs with three slightly divergent 6b genes (TE‐1‐6b‐L, TE‐1‐6b‐R and TE‐2‐6b) originating from a natural transformation event. In Arabidopsis thaliana, expression of 2×35S:TE‐2‐6b, but not 2×35S:TE‐1‐6b‐L or 2×35S:TE‐1‐6b‐R, led to plants with crinkly leaves, which strongly resembled mutants of the miR319a/TCP module. This module is composed of MIR319A and five CIN‐like TCP (TEOSINTHE BRANCHED1, CYCLOIDEA and PROLIFERATING CELL NUCLEAR ANTIGEN BINDING FACTOR) genes (TCP2, TCP3, TCP4, TCP10 and TCP24) targeted by miR319a. The CIN‐like TCP genes encode transcription factors and are required for cell division arrest at leaf margins during development. MIR319A overexpression causes excessive growth and crinkly leaves. TE‐2‐6b plants did not show increased miR319a levels, but the mRNA levels of the TCP4 target gene LOX2 were decreased, as in jaw‐D plants. Co‐expression of green fluorescent protein (GFP)‐tagged TCPs with native or red fluorescent protein (RFP)‐tagged TE‐6B proteins led to an increase in TCP protein levels and formation of numerous cytoplasmic dots containing 6B and TCP proteins. Yeast double‐hybrid experiments confirmed 6B/TCP binding and showed that TE‐1‐6B‐L and TE‐1‐6B‐R bind a smaller set of TCP proteins than TE‐2‐6B. A single nucleotide mutation in TE‐1‐6B‐R enlarged its TCP‐binding repertoire to that of TE‐2‐6B and caused a crinkly phenotype in Arabidopsis. Deletion analysis showed that TE‐2‐6B targets the TCP4 DNA‐binding domain and directly interferes with transcriptional activation. Taken together, these results provide detailed insights into the mechanism of action of the N. otophora TE‐encoded 6b genes. Significance Statement It was found previously that the Agrobacterium‐derived TE‐2‐6b gene from Nicotiana otophora induces strong growth effects in Nicotiana tabacum. However, the molecular mechanism has remained unknown. We show here that TE‐2‐6b induces a jaw‐D‐like phenotype in Arabidopsis – known to result from a decrease in CIN‐like TCPs – and that different TE‐6B proteins interact with different TCP subsets, thus providing insights into the molecular mechanism by which TE‐6B proteins stimulate plant growth.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>31659801</pmid><doi>10.1111/tpj.14591</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-1122-7684</orcidid><oa>free_for_read</oa></addata></record>
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1365-313X
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subjects 6b oncogene
Agrobacterium
Agrobacterium - metabolism
Antigens
Arabidopsis - metabolism
Arabidopsis - microbiology
Arabidopsis Proteins - antagonists & inhibitors
Arabidopsis Proteins - metabolism
Arabidopsis thaliana
Bacterial Proteins - metabolism
Binding
Cell division
Deoxyribonucleic acid
DNA
DNA, Bacterial - metabolism
Fluorescence
Gene expression
Gene Expression Profiling
Genes
Genetic transformation
Green fluorescent protein
Jaw
jaw‐D phenotype
Leaves
Microscopy, Confocal
Modules
Mutants
Mutation
natural transformant
Nicotiana - metabolism
Nicotiana - microbiology
Nicotiana otophora
Nucleotides
Original
Phenotypes
Plant Diseases - microbiology
Plant Leaves - metabolism
Plant Leaves - microbiology
Plants
Polymerase Chain Reaction
Proliferating cell nuclear antigen
Proteins
Red fluorescent protein
TCP genes
Transcription activation
Transcription factors
Transcription Factors - antagonists & inhibitors
Two-Hybrid System Techniques
Yeasts
title Inhibition of Arabidopsis thaliana CIN‐like TCP transcription factors by Agrobacterium T‐DNA‐encoded 6B proteins
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