Stem integrity in Arabidopsis thaliana requires a load-bearing epidermis

Author:

Asaoka Mariko12,Ooe Mao1,Gunji Shizuka13,Milani Pascale4,Runel Gaël4,Horiguchi Gorou56,Hamant Olivier27,Sawa Shinichiro8,Tsukaya Hirokazu9ORCID,Ferjani Ali13ORCID

Affiliation:

1. Department of Biology, Tokyo Gakugei University, 184-8501 Tokyo, Japan

2. Laboratoire de Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRAE, 69007 Lyon, France

3. United Graduated School of Education, Tokyo Gakugei University, 184-8501 Tokyo, Japan

4. BioMeca company, Ecole Normale Superieure de Lyon, 69007 Lyon, France

5. Department of Life Science, College of Science, Rikkyo University, 171-0021 Tokyo, Japan

6. Research Center for Life Science, College of Science, Rikkyo University, 171-0021 Tokyo, Japan

7. The International Research Organization for Advanced Science and Technology, Kumamoto University, 860-8555 Kumamoto, Japan

8. Graduate School of Science and Technology, Kumamoto University, 860-8555 Kumamoto, Japan

9. Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 113-0033 Tokyo, Japan

Abstract

ABSTRACT Because plant cells are glued to each other via their cell walls, failure to coordinate growth among adjacent cells can create cracks in tissues. Here, we find that the unbalanced growth of inner and outer tissues in the clavata3 de-etiolated3 (clv3 det3) mutant of Arabidopsis thaliana stretched epidermal cells, ultimately generating cracks in stems. Stem growth slowed before cracks appeared along clv3 det3 stems, whereas inner pith cells became drastically distorted and accelerated their growth, yielding to stress, after the appearance of cracks. This is consistent with a key role of the epidermis in restricting growth. Mechanical property measurements recorded using an atomic force microscope revealed that epidermal cell wall stiffness decreased in det3 and clv3 det3 epidermises. Thus, we hypothesized that stem integrity depends on the epidermal resistance to mechanical stress. To formally test this hypothesis, we used the DET3 gene as part of a tissue-specific strategy to complement cell expansion defects. Epidermis-driven DET3 expression restored growth and restored the frequency of stem cracking to 20% of the clv3 det3 mutant, demonstrating the DET3-dependent load-bearing role of the epidermis.

Funder

Ministry of Education, Culture, Sports, Science and Technology

European Research Council

Japan Society for the Promotion of Science

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

Reference51 articles.

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