4.8 Article

Transcriptional and Hormonal Regulation of Gravitropism of Woody Stems in Populus

Journal

PLANT CELL
Volume 27, Issue 10, Pages 2800-2813

Publisher

AMER SOC PLANT BIOLOGISTS
DOI: 10.1105/tpc.15.00531

Keywords

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Funding

  1. USDA AFRI [2011-67013-30062, 2015-67013-22891]
  2. NSF [IOS-1402064]
  3. NASA [NNX09AK82G]
  4. NIH [S10RR029668, S10RR027303]
  5. Direct For Biological Sciences
  6. Division Of Integrative Organismal Systems [1402064] Funding Source: National Science Foundation
  7. NASA [114151, NNX09AK82G] Funding Source: Federal RePORTER

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Angiosperm trees reorient their woody stems by asymmetrically producing a specialized xylem tissue, tension wood, which exerts a strong contractile force resulting in negative gravitropism of the stem. Here, we show, in Populus trees, that initial gravity perception and response occurs in specialized cells through sedimentation of starch-filled amyloplasts and relocalization of the auxin transport protein, PIN3. Gibberellic acid treatment stimulates the rate of tension wood formation and gravibending and enhances tissue-specific expression of an auxin-responsive reporter. Gravibending, maturation of contractile fibers, and gibberellic acid (GA) stimulation of tension wood formation are all sensitive to transcript levels of the Class I KNOX homeodomain transcription factor-encoding gene ARBORKNOX2 (ARK2). We generated genome-wide transcriptomes for trees in which gene expression was perturbed by gravistimulation, GA treatment, and modulation of ARK2 expression. These data were employed in computational analyses to model the transcriptional networks underlying wood formation, including identification and dissection of gene coexpression modules associated with wood phenotypes, GA response, and ARK2 binding to genes within modules. We propose a model for gravitropism in the woody stem in which the peripheral location of PIN3-expressing cells relative to the cambium results in auxin transport toward the cambium in the top of the stem, triggering tension wood formation, while transport away from the cambium in the bottom of the stem triggers opposite wood formation.

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