Plant cell identity. The role of position and lineage.
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Cell Division↗
Biomedical subjects
B Scheres
Publications and source records attributed to B Scheres.
Non-linear signaling for pattern formation?
Developmental pathways are often simplified as linear cascades of gene activation caused by initial signaling events. Recent data, however, support a more complex view in which non-linear responses to signals are important for pattern formation. First, a positive feedback loop may regulate cellular patterning in the Arabidopsis epidermis. Second, an asymmetric auxin distribution that organizes pattern in the distal root tip may be established by positive feedback.
Arabidopsis↗
An auxin-dependent distal organizer of pattern and polarity in the Arabidopsis root.
Root formation in plants involves the continuous interpretation of positional cues. Physiological studies have linked root formation to auxins. An auxin response element displays a maximum in the Arabidopsis root and we investigate its developmental significance. Auxin response mutants reduce the maximum or its perception, and interfere with distal root patterning. Polar auxin transport mutants affect its localization and distal pattern. Polar auxin transport inhibitors cause dramatic relocalization of the maximum, and associated changes in pattern and polarity. Auxin application and laser ablations correlate root pattern with a maximum adjacent to the vascular bundle. Our data indicate that an auxin maximum at a vascular boundary establishes a distal organizer in the root.
Arabidopsis↗
Plant development and signalling. Introduction.
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Evolution, Molecular↗
Digging out roots: pattern formation, cell division, and morphogenesis in plants.
The analysis of plant development by genetic, molecular, and surgical approaches has accumulated a large body of data, and yet it remains a challenge to uncover the basic mechanisms that are operating. Early steps of development, when the zygote and its daughter cells organize the embryonic plant, are poorly understood despite considerable efforts toward the identification of relevant genes. Reported cases of genetic redundancy suggest that the difficulty in uncovering patterning genes may reflect overlapping gene activities. Our current knowledge on plant embryo development still leaves open whether mechanisms for axis formation and subsequent pattern formation are fundamentally different in animals and plants. Axis formation may follow the general principle of establishing a peripheral asymmetric cue and mobilizing the cytoskeleton toward this cue--in the case of plants possibly located in the cell wall--but the molecules involved may be entirely different. Embryonic pattern formation involves the establishment of different domains, but although there are candidates, it is not clear whether genes that define these domains are identified yet. Pattern formation continues postembryonically in the meristem, and the flexibility of this process may be explained by a feed-forward system of patterning cues originating from more mature cells. Control of cell division and differentiation, which is important in the meristems--regions of continuous development--has been studied intensively and appears to involve short-range signaling and transmembrane receptor kinase activation. Finally, although high importance of control of cell division rates and planes for plant morphogenesis have been often inferred, recent genetic studies as well as comparative morphological data point to a less decisive role of cell division and to global controls of as yet unknown nature.
Body Patterning↗
Floral patterning. A LEAFY link from outer space.
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Arabidopsis↗
Root pattern: shooting in the dark?
Root pattern formation takes place in the embryo and is propagated through subsequent growth and development of the seedling root meristem. Pattern is maintained by positional cues and in some cases by local cell interactions. Such interactions are involved in the balance between cell division and differentiation in cells neighbouring the quiescent centre. This balancing act also occurs in the shoot in which the genetic circuitry underpinning this phenomenon has been characterised. The common genetic mechanism of patterned cell differentiation in the epidermis between the root and shoot extends these parallels further. Given that these shared mechanisms exist, it is tempting to speculate that they reflect the fact that roots may be derived, shoot structures. Alternatively such mechanisms may reflect an evolutionary convergence of genetic mechanism.
Body Patterning↗
Cell fate and cell differentiation status in the Arabidopsis root.
Post-embryonic development in plants is mainly achieved by its meristems. Within the Arabidopsis root meristem, both the fate and origin of its cells can be predicted with high accuracy. Mutants defective in the determination of root cell fates show that the corresponding genes are first required during embryogenesis. The sub-specification of cell fates, such as during epidermal root hair formation, involves transcription factors and phytohormones. In the Arabidopsis root, initial cell fate specification events must be followed by position-dependent reinforcement of cellular identity. A major question remains as to whether the signals that are involved in initiating the cellular pattern are the same or different from the signals used to reinforce it. The integrity of the root meristem is kept by balancing cell proliferation and cell differentiation, and differentiation-inhibiting signals originating from the quiescent centre are involved.
Arabidopsis↗
Root development: new meanings for root canals?
During Arabidopsis root development, a radial pattern of tissues is extended by the meristem. These tissues form continuous layers and recent data suggest that tissue continuity is instrumental for constraining the direction of signaling in a process termed channeling. In the ground tissue, fate-determining signals originate from contiguous cells of the same layer, possibly due to specific symplastic connections. Mutant analysis supports the hypothesis that vascular tissue continuity may facilitate and depend on the directional transport of a vascular fate-determining signal, possibly the phytohormone auxin.
Arabidopsis↗
The HOBBIT gene is required for formation of the root meristem in the Arabidopsis embryo.
In Arabidopsis, the root meristem originates from the hypophyseal cell and from an adjoining cell tier that is distinct at the heart stage of embryogenesis. We have analysed mutations in the HOBBIT (HBT) gene that is essential for root meristem formation. hbt embryos display incorrect hypophyseal cell development from the quadrant stage onward. At the heart stage, the adjoining cell tier of hbt embryos develops abnormally, in that the activation of cell division and the formation of a lateral root cap layer are disturbed. Strong hbt mutants give rise to seedlings that lack an anatomically recognisable quiescent centre and differentiated columella root cap cells, the cell types derived from the wild-type hypophysis. Furthermore, they have no mitotically active root meristem and lack a differentiated lateral root cap. Secondary roots of hbt mutants and roots obtained from cultured cells of hbt mutants have similar defects. Therefore the HBT gene is required for root meristem formation in different developmental contexts.
Arabidopsis↗
Short-range control of cell differentiation in the Arabidopsis root meristem.
Meristems are distinctive regions of plants that have capacity for continuous growth. Their developmental activity generates the majority of plant organs. It is currently unknown how cell division and cell differentiation are orchestrated in meristems, although genetic studies have demonstrated the relevance of a proper balance between the two processes. Root meristems contain a distinct central region of mitotically inactive cells, the quiescent centre, the function of which has remained elusive until now. Here we present laser ablation and genetic data that show that in Arabidopsis thaliana the quiescent centre inhibits differentiation of surrounding cells. Differentiation regulation occurs within the range of a single cell, in a manner strikingly similar to examples in animal development, such as during delamination of Drosophila neuroblasts. Our data indicate that pattern formation in the root meristem is controlled by a balance between short-range signals inhibiting differentiation and signals that reinforce cell fate decisions.
Arabidopsis↗
Cell signaling in root development.
Cell signaling has recently been shown to be of major importance in cell specification during Arabidopsis root development. In the ground tissue, cues of unknown molecular nature convey positional information and two genes provide an interesting link between asymmetric cell division and the determination of cell fate. In the root epidermis, cell specification involves ethylene signaling and transcription factors of which at least two are also required for cell fate decisions in the shoot epidermis.
Arabidopsis↗
Isolation and characterization of an auxin-inducible glutathione S-transferase gene of Arabidopsis thaliana.
Genes homologous to the auxin-inducible Nt103 glutathione S-transferase (GST) gene of tobacco, were isolated from a genomic library of Arabidopsis thaliana. We isolated a lambda clone containing an auxin-inducible gene, At103-1a, and part of a constitutively expressed gene, At103-1b. The coding regions of the Arabidopsis genes were highly homologous to each other and to the coding region of the tobacco gene but distinct from the GST genes that have been isolated from arabidopsis thusfar. Overexpression of a cDNA clone in Escherichia coli revealed that the AT103-1A protein had GST activity.
Amino Acid Sequence↗
The pea early nodulin gene PsENOD7 maps in the region of linkage group I containing sym2 and leghaemoglobin.
The early nodulin gene, PsENOD7, is expressed in pea root nodules induced by Rhizobium leguminosarum bv. viciae, but not in other plant organs. In situ hybridization showed that this gene is transcribed during nodule maturation in the infected cells of the proximal part of the prefixation zone II. At the transition of zone II into interzone II-III, the level of PsENOD7 mRNA drops markedly. PsENOD7 has no significant homology to other genes. RFLP mapping studies have shown that PsENOD7 is located in linkage group I between the leghaemoglobin genes and sym2.
Amino Acid Sequence↗
Cell fate in the Arabidopsis root meristem determined by directional signalling.
Postembryonic development in plants is achieved by apical meristems. Surgical studies and clonal analysis have revealed indirectly that cells in shoot meristems have no predictable destiny and that position is likely to play a role in the acquisition of cell identity. In contrast to animal systems, there has been no direct evidence for inductive signalling in plants until now. Here we present evidence for such signalling using laser ablation of cells in the root meristem of Arabidopsis thaliana. Although these cells show rigid clonal relationships, we now demonstrate that it is positional control that is most important in the determination of cell fate. Positional signals can be perpetuated from more mature to initial cells to guide the pattern of meristem cell differentiation. This offers an alternative to the general opinion that meristems are the source of patterning information.
Arabidopsis↗
Cellular organisation of the Arabidopsis thaliana root.
The anatomy of the developing root of Arabidopsis is described using conventional histological techniques, scanning and transmission electron microscopy. The root meristem is derived from cells of the hypophysis and adjacent cells of the embryo proper. The postembryonic organization of the root is apparent in the mature embryo and is maintained in the growing primary root after germination. Cell number and location is relatively invariant in the primary root, with 8 cortical and endodermal cell files but more variable numbers of pericycle and epidermal cells. The organisation of cells in lateral roots is similar to that of the primary root but with more variability in the numbers of cell files in each layer. [3H]thymidine labeling of actively growing roots indicates that a quiescent centre of four central cells (derived from the hypophysis) is located between the root cap columella and the stele. This plate of four cells is surrounded by three groups of cells in, proximal, distal and lateral positions. The labeling patterns of these cells suggest that they are the initials for the files of cells that comprise the root. They give rise to four sets of cell files: the stele, the cortex and endodermis, the epidermis and lateral root-cap and the columella. A model of meristem activity is proposed based on these data. This description of Arabidopsis root structure underpins future work on the developmental genetics of root morphogenesis.
Arabidopsis↗