Uncoupling FRUITFULL's functions through modification of a protein motif identified by co-ortholog analysis

Many plant transcription factors (TFs) are multifunctional and regulate growth and development in more than one tissue. These TFs can generally associate with different protein partners depending on the tissue type, thereby regulating tissue-specific target gene sets. However, how interaction specificity is ensured is still largely unclear. Here, we examine protein-protein interaction specificity using subfunctionalized co-orthologs of the FRUITFULL (FUL) subfamily of MADS-domain TFs. In Arabidopsis, FUL is multifunctional, playing important roles in flowering and fruiting, whereas these functions have partially been divided in the tomato co-orthologs FUL1 and FUL2. By linking protein sequence and function, we discovered a key amino acid motif that determines interaction specificity of MADS-domain TFs, which in Arabidopsis FUL determines the interaction with AGAMOUS and SEPALLATA proteins, linked to the regulation of a subset of targets. This insight offers great opportunities to dissect the biological functions of multifunctional MADS TFs.

Publication Details

Journal
Repository for Publications and Research Data (ETH Zurich)
Published
2024-11-27
DOI
https://doi.org/10.3929/ethz-b-000704822
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
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article

Uncoupling FRUITFULL's functions through modification of a protein motif identified by co-ortholog analysis

Repository for Publications and Research Data (ETH Zurich)
Plant Molecular Biology Research
article

Uncoupling FRUITFULL's functions through modification of a protein motif identified by co-ortholog analysis

article en

Abstract

Many plant transcription factors (TFs) are multifunctional and regulate growth and development in more than one tissue. These TFs can generally associate with different protein partners depending on the tissue type, thereby regulating tissue-specific target gene sets. However, how interaction specificity is ensured is still largely unclear. Here, we examine protein-protein interaction specificity using subfunctionalized co-orthologs of the FRUITFULL (FUL) subfamily of MADS-domain TFs. In Arabidopsis, FUL is multifunctional, playing important roles in flowering and fruiting, whereas these functions have partially been divided in the tomato co-orthologs FUL1 and FUL2. By linking protein sequence and function, we discovered a key amino acid motif that determines interaction specificity of MADS-domain TFs, which in Arabidopsis FUL determines the interaction with AGAMOUS and SEPALLATA proteins, linked to the regulation of a subset of targets. This insight offers great opportunities to dissect the biological functions of multifunctional MADS TFs.

Repository for Publications and Research Data (ETH Zurich)
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Plant Molecular Biology Research
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Uncoupling FRUITFULL's functions through modification of a protein motif identified by co-ortholog analysis · Repository for Publications and Research Data (ETH Zurich) (2024) | TGRS Research Map | TGRS