The intervening domain is required for DNA-binding and functional identity of plant MADS transcription factors

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作者
Xuelei Lai
Rosario Vega-Léon
Veronique Hugouvieux
Romain Blanc-Mathieu
Froukje van der Wal
Jérémy Lucas
Catarina S. Silva
Agnès Jourdain
Jose M. Muino
Max H. Nanao
Richard Immink
Kerstin Kaufmann
François Parcy
Cezary Smaczniak
Chloe Zubieta
机构
[1] Université Grenoble Alpes,Laboratoire Physiologie Cellulaire et Végétale
[2] CNRS,Plant Cell and Molecular Biology, Institute of Biology
[3] CEA,Bioscience, Wageningen Plant Research
[4] INRAE,Systems Biology of Gene Regulation, Institute of Biology
[5] IRIG-DBSCI-LPCV,European Synchrotron Radiation Facility
[6] Humboldt-Universität zu Berlin,Laboratory of Molecular Biology
[7] Wageningen University and Research,undefined
[8] European Molecular Biology Laboratory,undefined
[9] Humboldt-Universität zu Berlin,undefined
[10] Structural Biology Group,undefined
[11] Wageningen University and Research,undefined
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摘要
The MADS transcription factors (TF) are an ancient eukaryotic protein family. In plants, the family is divided into two main lineages. Here, we demonstrate that DNA binding in both lineages absolutely requires a short amino acid sequence C-terminal to the MADS domain (M domain) called the Intervening domain (I domain) that was previously defined only in type II lineage MADS. Structural elucidation of the MI domains from the floral regulator, SEPALLATA3 (SEP3), shows a conserved fold with the I domain acting to stabilise the M domain. Using the floral organ identity MADS TFs, SEP3, APETALA1 (AP1) and AGAMOUS (AG), domain swapping demonstrate that the I domain alters genome-wide DNA-binding specificity and dimerisation specificity. Introducing AG carrying the I domain of AP1 in the Arabidopsis ap1 mutant resulted in strong complementation and restoration of first and second whorl organs. Taken together, these data demonstrate that the I domain acts as an integral part of the DNA-binding domain and significantly contributes to the functional identity of the MADS TF.
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