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<p>Twisted growth serves myriad adaptive functions in plants. Unlike animal motions, plant motions require symmetry breaking during growth and typically involve microtubule-related genes. But how macroscopic twisting emerges from molecular-level perturbations remains&#xa0;unclear. Here, we show that microtubule-based symmetry breaking propagates across multiple organizational scales via the epidermis to produce handed root skewing. At the nanoscale, aberrant patterning of cellulose microfibrils is associated with microscale skewed cell expansion, both of which precede the millimeter scale emergence of helical epidermal cell files. The resulting chiral torsion of the epidermis mediates organ level symmetry breaking in the form of whole-root skewing through macroscale interactions between the root and its surrounding environment. We demonstrate the dominant role of the epidermis by complementation of microtubule activity in the epidermis alone, which is sufficient to restore transverse cortical microtubule orientation, wild-type-like morphology in cortical cells, and straight root growth.</p>

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The epidermis coordinates multi-scale symmetry breaking in chiral root growth

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年12月10日

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  • Natasha Nolan,
  • Leila Jaafar,
  • Yuanwei Fan,
  • Yuxuan Huang,
  • Lily Murchison,
  • Juliana Ocasio,
  • Joyce G. Onyenedum,
  • Charles T. Anderson,
  • Guy M. Genin,
  • Ram Dixit

摘要

Twisted growth serves myriad adaptive functions in plants. Unlike animal motions, plant motions require symmetry breaking during growth and typically involve microtubule-related genes. But how macroscopic twisting emerges from molecular-level perturbations remains unclear. Here, we show that microtubule-based symmetry breaking propagates across multiple organizational scales via the epidermis to produce handed root skewing. At the nanoscale, aberrant patterning of cellulose microfibrils is associated with microscale skewed cell expansion, both of which precede the millimeter scale emergence of helical epidermal cell files. The resulting chiral torsion of the epidermis mediates organ level symmetry breaking in the form of whole-root skewing through macroscale interactions between the root and its surrounding environment. We demonstrate the dominant role of the epidermis by complementation of microtubule activity in the epidermis alone, which is sufficient to restore transverse cortical microtubule orientation, wild-type-like morphology in cortical cells, and straight root growth.