Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
, 4

Planting Molecular Functions in an Ecological Context With Arabidopsis Thaliana

Affiliations
Review

Planting Molecular Functions in an Ecological Context With Arabidopsis Thaliana

Ute Krämer. Elife.

Abstract

The vascular plant Arabidopsis thaliana is a central genetic model and universal reference organism in plant and crop science. The successful integration of different fields of research in the study of A. thaliana has made a large contribution to our molecular understanding of key concepts in biology. The availability and active development of experimental tools and resources, in combination with the accessibility of a wealth of cumulatively acquired knowledge about this plant, support the most advanced systems biology approaches among all land plants. Research in molecular ecology and evolution has also brought the natural history of A. thaliana into the limelight. This article showcases our current knowledge of the natural history of A. thaliana from the perspective of the most closely related plant species, providing an evolutionary framework for interpreting novel findings and for developing new hypotheses based on our knowledge of this plant.

Keywords: Arabidopsis relatives; arabidopsis; ecology; natural history; plant biology; the natural history of model organisms.

Conflict of interest statement

The author declares that no competing interests exist.

Figures

Figure 1.
Figure 1.. Life cycle of Arabidopsis thaliana.
(A) A. thaliana of the accession Columbia (Col) at different stages of its life cycle, from seed (bottom left) to seedling (11 days), to vegetative growth (39 days), and to reproductive growth (45 days). Photographs of (B) a flower, (C) a pollen grain (scanning electron micrograph), and (D) mature siliques (seed pods; left: closed; right: open with a few remaining unshattered seeds) at higher magnification. Image credits: B and C, Maria Bernal and Peter Huijser; other photographs, Ines Kubigsteltig and Klaus Hagemann. DOI: http://dx.doi.org/10.7554/eLife.06100.002
Figure 2.
Figure 2.. A. thaliana and a subset of species from its sister clade.
From left to right: A. thaliana (Col), A. halleri (ssp. halleri; individual Lan5, Langelsheim, Harz, Germany), A. lyrata (ssp. lyrata; selfing accession Great Lakes, North America), and A. croatica (Baške Oštarje/Ljubičko Brdo, Croatia). A. thaliana was grown from seed to early reproductive stage, and the other species were propagated vegetatively and grown for 3–6 months. The individuals shown here do not reflect the large within-species morphological diversity, particularly in leaf shape, among different accessions of A. halleri and A. lyrata. Image credit: Ute Krämer and Klaus Hagemann. DOI: http://dx.doi.org/10.7554/eLife.06100.004
Figure 3.
Figure 3.. Map of A. thaliana worldwide distribution.
Areas colored in red correspond to the continuous distribution of A. thaliana; red circles mark additional sites. This map is based on a partial map kindly provided by Matthias Hoffmann (personal communication, November 2014), with manual additions to the southern hemisphere (Bresinsky et al., 2008). Image credit: Ute Krämer and Klaus Hagemann. DOI: http://dx.doi.org/10.7554/eLife.06100.005
Figure 4.
Figure 4.. The simple anatomy of A. thaliana roots.
Longitudinal (left) and transverse (right) confocal sections of A. thaliana roots. Green fluorescence highlights the plasma membrane of the pericycle cells of an A. thaliana hma2hma4 double mutant line (Sinclair et al., 2007) (accession Wassilewskija). Red fluorescence of propidium iodide (PI) as a stain is overlaid to visualize cell walls. The root cell layers (consecutive outward to inward) are: epidermis (e), cortex (c), endodermis (n) and pericycle (p). Note that the Casparian Strip surrounding the endodermis cells forms an apoplastic diffusion barrier (Roppolo et al., 2011) that blocks the movement of PI further inward. Image credit: Ute Krämer and Scott A. Sinclair. DOI: http://dx.doi.org/10.7554/eLife.06100.006

Similar articles

See all similar articles

Cited by 4 PubMed Central articles

References

    1. Abel S. Phosphate sensing in root development. Current Opinion in Plant Biology. 2011;14:303–309. doi: 10.1016/j.pbi.2011.04.007. - DOI - PubMed
    1. Alonso-Blanco C, Aarts MG, Bentsink L, Keurentjes JJ, Reymond M, Vreugdenhil D, Koornneef M. What has natural variation taught us about plant development, physiology, and adaptation? The Plant Cell. 2009;21:1877–1896. doi: 10.1105/tpc.109.068114. - DOI - PMC - PubMed
    1. Al-Shehbaz IA, O'Kane SL. The Arabidopsis Book. The American Society of Plant Biologists; 2002. Taxonomy and phylogeny of Arabidopsis (Brassicaceae) pp. 1–22.
    1. Andres F, Coupland G. The genetic basis of flowering responses to seasonal cues. Nature Reviews Genetics. 2012;13:627–639. doi: 10.1038/nrg3291. - DOI - PubMed
    1. Arabidopsis Genome Initiative Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature. 2000;408:796–815. doi: 10.1038/35048692. - DOI - PubMed

Publication types

Grant support

The funder had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Feedback