Four-dimensional phenotyping reveals MYOSIN XI-dependent establishment of branch morphology through upward- and stably-directed growth in Arabidopsis

Plants develop characteristic shoot architectures by extending branches at specific angles. Primary shoots bend in response to gravity and then adjust the orientation through an organ-straightening process to achieve a mechanically favorable shape. However, how plants integrate branch structure with the shoot architecture remains uncertain. Here, we examined the lateral branch morphology of <i>Arabidopsis thaliana</i> mutants for myosin XI motor proteins through a combination of three-dimensional reconstruction and temporal imaging. The wild type and <i>myosin xif</i> mutant formed S-shaped branches and gradually adjusted the branch angle upwards. The <i>myosin xik</i> mutant exhibited straighter and drooping branches and maintained branch angles. The <i>myosin xif xik</i> double mutant formed branches with irregular directional changes with fluctuating angles. These results suggest that MYOSIN XIk and XIf are required for the establishment of branch morphology through upward bending, stabilizing growth direction, and maintaining curvature.

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Publication Details

Journal
Quantitative Plant Biology
Published
2025-01-01
DOI
https://doi.org/10.1017/qpb.2025.10007
Citations
1
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
1.75

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article

Four-dimensional phenotyping reveals MYOSIN XI-dependent establishment of branch morphology through upward- and stably-directed growth in Arabidopsis

Takumi Higaki, Itsuki Kunita, Daichi Yoshida, Haruko Ueda et al.
1 citations
Quantitative Plant Biology
Plant Molecular Biology Research
1.75
article

Four-dimensional phenotyping reveals MYOSIN XI-dependent establishment of branch morphology through upward- and stably-directed growth in Arabidopsis

Takumi Higaki, Itsuki Kunita, Daichi Yoshida, Haruko Ueda, Masashi Toda
article en
1 citations

Abstract

Plants develop characteristic shoot architectures by extending branches at specific angles. Primary shoots bend in response to gravity and then adjust the orientation through an organ-straightening process to achieve a mechanically favorable shape. However, how plants integrate branch structure with the shoot architecture remains uncertain. Here, we examined the lateral branch morphology of <i>Arabidopsis thaliana</i> mutants for myosin XI motor proteins through a combination of three-dimensional reconstruction and temporal imaging. The wild type and <i>myosin xif</i> mutant formed S-shaped branches and gradually adjusted the branch angle upwards. The <i>myosin xik</i> mutant exhibited straighter and drooping branches and maintained branch angles. The <i>myosin xif xik</i> double mutant formed branches with irregular directional changes with fluctuating angles. These results suggest that MYOSIN XIk and XIf are required for the establishment of branch morphology through upward bending, stabilizing growth direction, and maintaining curvature.

Quantitative Plant BiologyVol. 6
Konan University (JP), University of the Ryukyus (JP), Kumamoto University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 15%
Plant Molecular Biology Research
1.75
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