» Articles » PMID: 38434638

Tapping into the Plasticity of Plant Architecture for Increased Stress Resilience

Overview
Journal F1000Res
Date 2024 Mar 4
PMID 38434638
Authors
Affiliations
Soon will be listed here.
Abstract

Plant architecture develops post-embryonically and emerges from a dialogue between the developmental signals and environmental cues. Length and branching of the vegetative and reproductive tissues were the focus of improvement of plant performance from the early days of plant breeding. Current breeding priorities are changing, as we need to prioritize plant productivity under increasingly challenging environmental conditions. While it has been widely recognized that plant architecture changes in response to the environment, its contribution to plant productivity in the changing climate remains to be fully explored. This review will summarize prior discoveries of genetic control of plant architecture traits and their effect on plant performance under environmental stress. We review new tools in phenotyping that will guide future discoveries of genes contributing to plant architecture, its plasticity, and its contributions to stress resilience. Subsequently, we provide a perspective into how integrating the study of new species, modern phenotyping techniques, and modeling can lead to discovering new genetic targets underlying the plasticity of plant architecture and stress resilience. Altogether, this review provides a new perspective on the plasticity of plant architecture and how it can be harnessed for increased performance under environmental stress.

Citing Articles

Advances in Understanding Drought Stress Responses in Rice: Molecular Mechanisms of ABA Signaling and Breeding Prospects.

Ma Y, Tang M, Wang M, Yu Y, Ruan B Genes (Basel). 2025; 15(12.

PMID: 39766796 PMC: 11675997. DOI: 10.3390/genes15121529.


Sugar Transport and Signaling in Shoot Branching.

Doidy J, Wang Y, Gouaille L, Goma-Louamba I, Jiang Z, Pourtau N Int J Mol Sci. 2024; 25(23.

PMID: 39684924 PMC: 11641904. DOI: 10.3390/ijms252313214.

References
1.
Lewis D, Negi S, Sukumar P, Muday G . Ethylene inhibits lateral root development, increases IAA transport and expression of PIN3 and PIN7 auxin efflux carriers. Development. 2011; 138(16):3485-95. DOI: 10.1242/dev.065102. View

2.
Nakamura A, Umemura I, Gomi K, Hasegawa Y, Kitano H, Sazuka T . Production and characterization of auxin-insensitive rice by overexpression of a mutagenized rice IAA protein. Plant J. 2006; 46(2):297-306. DOI: 10.1111/j.1365-313X.2006.02693.x. View

3.
Fusi R, Rosignoli S, Lou H, Sangiorgi G, Bovina R, Pattem J . Root angle is controlled by in cereal crops employing an antigravitropic mechanism. Proc Natl Acad Sci U S A. 2022; 119(31):e2201350119. PMC: 9351459. DOI: 10.1073/pnas.2201350119. View

4.
Lucob-Agustin N, Sugiura D, Kano-Nakata M, Hasegawa T, Suralta R, Niones J . The promoted lateral root 1 (plr1) mutation is involved in reduced basal shoot starch accumulation and increased root sugars for enhanced lateral root growth in rice. Plant Sci. 2020; 301:110667. DOI: 10.1016/j.plantsci.2020.110667. View

5.
Bittisnich D, Williamson R . Tip-localised H(+)-fluxes and the applicability of the acid-growth hypothesis to tip-growing cells: Control of chloronemal extension in Funaria hygrometrica by auxin and light. Planta. 2013; 178(1):96-102. DOI: 10.1007/BF00392532. View