The Root of the Problem: Developmental processes can define repeated patterns of structure, such as somites in vertebrates. In plants, too, repeated structures arise during growth and development. As the above-ground shoot grows, it sends out leaves or branches at intervals guided by hormone signaling. As the below-ground root grows, it too ramifies, sending out lateral roots. Moreno-Risueno et al. (p. 1306 ; see the Perspective by Traas and Vernoux ) explored the expression of genes underlying development of lateral roots and found that oscillations in gene expression guide the specification of lateral roots.

This article deals with the origin and evolution of the DOF transcription factor family through a phylogenetic analysis of those DOF sequences identified from a variety of representative organisms from different taxonomic groups: the green unicellular alga Chlamydomonas reinhardtii, the moss Physcomitrella patens, the fern Selaginella moellendorffii, the gymnosperm Pinus taeda, the dicotyledoneous Arabidopsis thaliana and the monocotyledoneous angiosperms Oryza sativa and Hordeum vulgare. In barley, we have identified 26 different DOF genes by sequence analyses of clones isolated from the screening of genomic libraries and of ESTs, whereas a single DOF gene was identified by bioinformatics searches in the Chlamydomonas genome. The phylogenetic analysis groups all these genes into six major clusters of orthologs originated from a primary basal grade. Our results suggest that duplications of an ancestral DOF, probably formed in the photosynthetic eukaryotic ancestor, followed by subsequent neo-, sub-functionalization and pseudogenization processes would have triggered the expansion of the DOF family. Loss, acquisition and shuffling of conserved motifs among the new DOFs likely underlie the mechanism of formation of the distinct subfamilies.

Significance: The process by which cells differentiate is central to multicellular development and cancer. Dramatic gene expression changes mediate this complex process, which involves the termination of proliferation and the acquisition of distinct cell-specific features. We identified a transcription factor, MYB DOMAIN PROTEIN 36 (MYB36), that regulates this developmental transition in the Arabidopsis thaliana root endodermis. Differentiated endodermis forms a protective waxy barrier called the Casparian strip. We found that MYB36 activates genes involved in Casparian strip formation and represses genes involved in proliferation. Our results suggest that MYB36 is a critical regulator of developmental timing in the root endodermis.

Summary: In nature roots grow in the dark and away from light (negative phototropism). However, most current research in root biology has been carried out with the root system grown in the presence of light. Here, we have engineered a device, called Dark‐Root (D‐Root), to grow plants in vitro with the aerial part exposed to the normal light/dark photoperiod while the roots are in the dark or exposed to specific wavelengths or light intensities. D‐Root provides an efficient system for cultivating a large number of seedlings and easily characterizing root architecture in the dark. At the morphological level, root illumination shortens root length and promotes early emergence of lateral roots, therefore inducing expansion of the root system. Surprisingly, root illumination also affects shoot development, including flowering time. Our analyses also show that root illumination alters the proper response to hormones or abiotic stress (e.g. salt or osmotic stress) and nutrient starvation, enhancing inhibition of root growth. In conclusion, D‐Root provides a growing system closer to the natural one for assaying Arabidopsis plants, and therefore its use will contribute to a better understanding of the mechanisms involved in root development, hormonal signaling and stress responses.