Evolution of a SHOOTMERISTEMLESS transcription factor binding site promotes fruit shape determination

In animals and plants, organ shape is primarily determined during primordium development by carefully coordinated growth and cell division<sup>1-3</sup>. Rare examples of post-primordial change in morphology (reshaping) exist that offer tractable systems for the study of mechanisms required for organ shape determination and diversification. One such example is morphogenesis in Capsella fruits whose heart-shaped appearance emerges by reshaping of the ovate spheroid gynoecium upon fertilization<sup>4</sup>. Here we use whole-organ live-cell imaging and single-cell RNA sequencing (scRNA-seq) analysis to show that Capsella fruit shape determination is based on dynamic changes in cell growth and cell division coupled with local maintenance of meristematic identity. At the molecular level, we reveal an auxin-induced mechanism that is required for morphological alteration and ultimately determined by a single cis-regulatory element. This element resides in the promoter of the Capsella rubella SHOOTMERISTEMLESS<sup>5</sup> (CrSTM) gene. The CrSTM meristem identity factor positively regulates its own expression through binding to this element, thereby providing a feed-forward loop at the position and time of protrusion emergence to form the heart. Independent evolution of the STM-binding element in STM promoters across Brassicaceae species correlates with those undergoing a gynoecium-to-fruit shape change. Accordingly, genetic and phenotypic studies show that the STM-binding element is required to facilitate the shape transition and suggest a conserved molecular mechanism for organ morphogenesis.

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Publication Details

Journal
Nature Plants
Published
2024-12-12
DOI
https://doi.org/10.1038/s41477-024-01854-1
Citations
9
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
5.40

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article

Evolution of a SHOOTMERISTEMLESS transcription factor binding site promotes fruit shape determination

Mateusz Majda, Yang Dong, Tongbing Su, Lars Østergaard et al.
9 citations
Nature Plants
Plant Molecular Biology Research
5.40
article

Evolution of a SHOOTMERISTEMLESS transcription factor binding site promotes fruit shape determination

Mateusz Majda, Yang Dong, Tongbing Su, Lars Østergaard, Richard S. Smith, Guixia Xu, Tian‐Feng Lü, Feng Gao, Hao-Ran Sun, Quan Yuan, Yao Zhang, Yining Ding, Zhi-Cheng Hu
article en
9 citations

Abstract

In animals and plants, organ shape is primarily determined during primordium development by carefully coordinated growth and cell division<sup>1-3</sup>. Rare examples of post-primordial change in morphology (reshaping) exist that offer tractable systems for the study of mechanisms required for organ shape determination and diversification. One such example is morphogenesis in Capsella fruits whose heart-shaped appearance emerges by reshaping of the ovate spheroid gynoecium upon fertilization<sup>4</sup>. Here we use whole-organ live-cell imaging and single-cell RNA sequencing (scRNA-seq) analysis to show that Capsella fruit shape determination is based on dynamic changes in cell growth and cell division coupled with local maintenance of meristematic identity. At the molecular level, we reveal an auxin-induced mechanism that is required for morphological alteration and ultimately determined by a single cis-regulatory element. This element resides in the promoter of the Capsella rubella SHOOTMERISTEMLESS<sup>5</sup> (CrSTM) gene. The CrSTM meristem identity factor positively regulates its own expression through binding to this element, thereby providing a feed-forward loop at the position and time of protrusion emergence to form the heart. Independent evolution of the STM-binding element in STM promoters across Brassicaceae species correlates with those undergoing a gynoecium-to-fruit shape change. Accordingly, genetic and phenotypic studies show that the STM-binding element is required to facilitate the shape transition and suggest a conserved molecular mechanism for organ morphogenesis.

Nature PlantsVol. 11(1)
John Innes Centre (GB), Chinese Academy of Sciences (CN), Beijing Botanical Garden (CN), University of Oxford (GB), Beijing Academy of Agricultural and Forestry Sciences (CN), Institute of Botany (CN), University of Chinese Academy of Sciences (CN), China National Botanical Garden, University of Lausanne (CH)
National Natural Science Foundation of China, Directorate for Biological Sciences, Biotechnology and Biological Sciences Research Council, National Key Research and Development Program of China
Life in Land
Openalex Percentile: Top 5%
Plant Molecular Biology Research
5.40
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