Seedlings of zea mays l. (poaceae) and pterogyne nitens tul. (fabaceae): Morphoanatomic and terminological considerations / Plântulas de zea mays l. (poaceae) e pterogyne nitens tul. (fabaceae): Considerações morfoanatômicas e terminológicas

Seedlings of Zea mays L. (maize), Poaceae, and Pterogyne nitens Tul. (wild peanut), Leguminosae, are described morphologically and anatomically in order to characterize the species, but particularly to disseminate the terminology about the seedling, which is little known by non-specialist researchers and undergraduate students. Seedlings were obtained in the laboratory, using Petri dishes. Seedling was considered as the initial plant development phase, which comprises the period from germination to formation of the eophyll. Zea mays seedling is hypogeal and cryptocotyledonous, and it consists of coleorhiza, considered the primary root, endogenous embryonic root, commonly considered in the literature as radicle, reduced hypocotyl, and coleoptile, considered here as eophyll. The second seedling leaf of Z. mays is made up of uniseriate epidermis and homogeneous mesophyll. Pterogyne nitens exhibits epigeal and phanerocotyledonous seedling, and consists of primary root, long hypocotyl, two cotyledons, epicotyl, and opposite eophylls difoliolated or trifoliolated. The hypocotyl has root/shoot transition structure and the eophylls are dorsiventral consisting of one cell layer palisade parenchyma and pluriseriate spongy parenchyma. Seedlings of both species show significant morphological and anatomical differences and specific terminology, especially that of Z. mays.

Bootstrapping and Pinning down the Root Meristem; the Auxin–PLT–ARR Network Unites Robustness and Sensitivity in Meristem Growth Control

After germination, the meristem of the embryonic plant root becomes activated, expands in size and subsequently stabilizes to support post-embryonic root growth. The plant hormones auxin and cytokinin, together with master transcription factors of the PLETHORA (PLT) family have been shown to form a regulatory network that governs the patterning of this root meristem. Still, which functional constraints contributed to shaping the dynamics and architecture of this network, has largely remained unanswered. Using a combination of modeling approaches we reveal how the interplay between auxin and PLTs enables meristem activation in response to above-threshold stimulation, while its embedding in a PIN-mediated auxin reflux loop ensures localized PLT transcription and thereby, a finite meristem size. We furthermore demonstrate how this constrained PLT transcriptional domain enables independent control of meristem size and division rates, further supporting a division of labor between auxin and PLT. We subsequently reveal how the weaker auxin antagonism of the earlier active Arabidopsis response regulator 12 (ARR12) may arise from the absence of a DELLA protein interaction domain. Our model indicates that this reduced strength is essential to prevent collapse in the early stages of meristem expansion while at later stages the enhanced strength of Arabidopsis response regulator 1 (ARR1) is required for sufficient meristem size control. Summarizing, our work indicates that functional constraints significantly contribute to shaping the auxin–cytokinin–PLT regulatory network.

The expression pattern of OsDim1 in rice and its proposed function

Development of plant tissues is dependent on numerous factors, including hormone activity, signaling, cell division, and elongation. In plants, Defective Entry into Mitosis 1 (Dim1) homologs are recognized as pivotal in leaf senescence and progress of normal growth, but their role in rice has not been functionally characterized. The findings presented in this paper suggest that OsDim1 is important in early seedling development, pollen tube elongation, and impacts rice yield components. The gene is expressed in the scutellum, endosperm, embryonic root, shoot, pollen grains and tubes, as well as in several organs of the rice flower. According to the present study findings, RNAi mediated knockdown of OsDim1 resulted in phytohormonal imbalance, reduced amylase activity, affected differentiation of embryonic root elongation zone tissues, suppressed embryonic root and shoot growth, and impaired pollen tube elongation. In contrast, overexpression of OsDim1 showed significant growth in embryonic roots and shoots, while it increased culm length, total number of tillers per plant, seed setting rate, and total number of grains per panicle compared to its wild type line. In summary, we propose OsDim1 plays an important role in seedling growth and pollen tube elongation, and has pleiotropic effects on reproductive tissues.

Two Wheat Cultivars with Contrasting Post-Embryonic Root Biomass Differ in Shoot Re-Growth after Defoliation: Implications for Breeding Grazing Resilient Forages

The ability of forages to quickly resume aboveground growth after grazing is a trait that enables farmers to better manage their livestock for maximum profitability. Leaf removal impairs root growth. As a consequence of a deficient root system, shoot re-growth is inhibited leading to poor pasture performance. Despite the importance of roots for forage productivity, they have not been considered as breeding targets for improving grazing resilience due in large part to the lack of knowledge on the relationship between roots and aboveground biomass re-growth. Winter wheat (Triticum aestivum) is extensively used as forage source in temperate climates worldwide. Here, we investigated the impact of leaf clipping on specific root traits, and how these influence shoot re-growth in two winter wheat cultivars (i.e., Duster and Cheyenne) with contrasting root and shoot biomass. We found that root growth angle and post-embryonic root growth in both cultivars are strongly influenced by defoliation. We discovered that Duster, which had less post-embryonic roots before defoliation, reestablished its root system faster after leaf cutting compared with Cheyenne, which had a more extensive pre-defoliation post-embryonic root system. Rapid resumption of root growth in Duster after leaf clipping was associated with faster aboveground biomass re-growth even after shoot overcutting. Taken together, our results suggest that lower investments in the production of post-embryonic roots presents an important ideotype to consider when breeding for shoot re-growth vigor in dual purpose wheat.

What Makes Adventitious Roots?

The spermatophyte root system is composed of a primary root that develops from an embryonically formed root meristem, and of different post-embryonic root types: lateral and adventitious roots. Adventitious roots, arising from the stem of the plants, are the main component of the mature root system of many plants. Their development can also be induced in response to adverse environmental conditions or stresses. Here, in this review, we report on the morphological and functional diversity of adventitious roots and their origin. The hormonal and molecular regulation of the constitutive and inducible adventitious root initiation and development is discussed. Recent data confirmed the crucial role of the auxin/cytokinin balance in adventitious rooting. Nevertheless, other hormones must be considered. At the genetic level, adventitious root formation integrates the transduction of external signals, as well as a core auxin-regulated developmental pathway that is shared with lateral root formation. The knowledge acquired from adventitious root development opens new perspectives to improve micropropagation by cutting in recalcitrant species, root system architecture of crops such as cereals, and to understand how plants adapted during evolution to the terrestrial environment by producing different post-embryonic root types.