Properties of the primary organization field in the embryo of Xenopus laevis

Development ◽  
1973 ◽  
Vol 30 (2) ◽  
pp. 283-300
Author(s):  
J. Cooke
Keyword(s):  
Organizer Region ◽  
Positional Information ◽  
Host Cells ◽  
Normal Embryo ◽  
Tail Bud ◽  
Essentially Normal ◽  
Head Formation ◽  
Source Data ◽  
Primary Organization ◽  
Host Embryo

Patterns of individuation occurring in the primary embryonic axis of Xenopus following excision of the organizer region of the early gastrula are described. In some 70% of cases the information for induction of the complete head is qualitatively restored by the time of cell determination, giving rise to an essentially normal embryo. In some 40% of cases a second posterior axis of bilaterality is formed, causing development of a secondary anus, tail-fin and spinal cord, and often somites. The probabilities of twinning in the tailfield and of failure to complete apical regulation (= head formation) are largely independent. After such excision of the head organizer region, a delay of some 3 h in the schedule of visible differentiation in the neurula/tail-bud embryo is commonly incurred, whether or not apical regulation is successful. When the apex is excised from a host embryo which has already contained for some hours a second apex (= head organizer) as described in an earlier paper, that grafted apex then captures a considerably increased territory in the host material, as seen from the size of the individuation field finally caused by it. Such a shift across host cells, of the boundary between fields of positional information due to two organizers, is not seen under any conditions where these are left intact, or where host excision is carried out soon after implanting the donor organizer. In discussing the results and reconciling them with earlier observations, it is shown that they strongly suggest the presence of local polar (i.e. vectorial) properties in the presumptive mesoderm, due to signals from restricted regions which have achieved a special apical state. Repolarization of cells by a new organizer is not very rapid, and may spread decrementally from the source. Data on further delays in development, caused by the presence of the second organizer during regulation in the host apex, suggest that one organizer may act directly on cells elsewhere to delay or prevent the restoration of the apical state there.

Properties of the primary organization field in the embryo of Xenopus laevis

Development ◽  
1972 ◽  
Vol 28 (1) ◽  
pp. 27-46
Author(s):  
J. Cooke
Keyword(s):  
Early Stage ◽  
Organizer Region ◽  
Positional Information ◽  
Bilateral Symmetry ◽  
Angular Distance ◽  
Organ Differentiation ◽  
Primary Organization ◽  
Cell Commitment ◽  
Time Of Operation ◽  
Field Formation

The results are reported of a series of experiments, the exact geometry of which has been presented in a previous paper. Late blastulae and early stage-10 gastrulae are supplied with a second head organizer region at varying angular distances, in the marginal zone, from the presumptive site of their own organizer. The configuration of positional information existing in the mesodermal mantle of the late gastrula or earliest neurula, as a final result of such operations, was recorded by observing the pattern of axial organ differentiation obtained by tailbud stages (26–28). The operational differences between various current theories as to the nature of embryonic differentiation fields are briefly discussed, as a framework within which to consider the results of experiments such as those reported here. It is suggested that in the future, and using the present results as a basis, experiments may be possible that are more critical in distinguishing between the various theoretical suppositions involved. Evidence is presented that the final configuration of positional information, achieved as a result of the implantation of a second head organizer at or before the onset of host gastrulation, becomes stable some time before it is irreversibly expressed in terms of a pattern of cell commitment in the mesodermal/endodermal mantle. It is insensitive both to relative ages of host and graft at the time of operation, over the range employed and, probably, to the ambient temperature of development between operation and the time of cell differentiation, being dependent only on the angular distance originally existing between graft and presumptive host organizer sites. In the discussion, a model is given for the visualization of positional information in partially double fields, produced in a two-dimensional sheet of cells where the normal end-point of field formation is a bilateral symmetry of differentiation zones.

Axis-inducing activities and cell fates of the zebrafish organizer

Development ◽  
2000 ◽  
Vol 127 (16) ◽  
pp. 3407-3417 ◽  
Author(s):  
L. Saude ◽  
K. Woolley ◽  
P. Martin ◽  
W. Driever ◽  
D.L. Stemple
Keyword(s):  
Organizer Region ◽  
Complete Removal ◽  
Floor Plate ◽  
Significant Loss ◽  
Cell Fates ◽  
Deep Tissue ◽  
Head Formation ◽  
Prechordal Plate ◽  
Embryonic Shield ◽  
Organizer Activity

We have investigated axis-inducing activities and cellular fates of the zebrafish organizer using a new method of transplantation that allows the transfer of both deep and superficial organizer tissues. Previous studies have demonstrated that the zebrafish embryonic shield possesses classically defined dorsal organizer activity. When we remove the morphologically defined embryonic shield, embryos recover and are completely normal by 24 hours post-fertilization. We find that removal of the morphological shield does not remove all goosecoid- and floating head-expressing cells, suggesting that the morphological shield does not comprise the entire organizer region. Complete removal of the embryonic shield and adjacent marginal tissue, however, leads to a loss of both prechordal plate and notochord. In addition, these embryos are cyclopean, show a significant loss of floor plate and primary motorneurons and display disrupted somite patterning. Motivated by apparent discrepancies in the literature we sought to test the axis-inducing activity of the embryonic shield. A previous study suggested that the shield is capable of only partial axis induction, specifically being unable to induce the most anterior neural tissues. Contrary to this study, we find shields can induce complete secondary axes when transplanted into host ventral germ-ring. In induced secondary axes donor tissue contributes to notochord, prechordal plate and floor plate. When explanted shields are divided into deep and superficial fragments and separately transplanted we find that deep tissue is able to induce the formation of ectopic axes with heads but lacking posterior tissues. We conclude that the deep tissue included in our transplants is important for proper head formation.

A developmental pathway controlling outgrowth of the Xenopus tail bud

Development ◽  
1999 ◽  
Vol 126 (8) ◽  
pp. 1611-1620 ◽  
Author(s):  
C.W. Beck ◽  
J.M. Slack
Keyword(s):  
Normal Development ◽  
Posterior Part ◽  
Neural Plate ◽  
General Mechanism ◽  
Developmental Pathway ◽  
Tail Bud ◽  
Neural Tubes ◽  
Tailbud Stage ◽  
Tail Tip ◽  
Host Embryo

We have developed a new assay to identify factors promoting formation and outgrowth of the tail bud. A piece of animal cap filled with the test mRNAs is grafted into the posterior region of the neural plate of a host embryo. With this assay we show that expression of a constitutively active Notch (Notch ICD) in the posterior neural plate is sufficient to produce an ectopic tail consisting of neural tube and fin. The ectopic tails express the evenskipped homologue Xhox3, a marker for the distal tail tip. Xhox3 will also induce formation of an ectopic tail in our assay. We show that an antimorphic version of Xhox3, Xhox3VP16, will prevent tail formation by Notch ICD, showing that Xhox3 is downstream of Notch signalling. An inducible version of this reagent, Xhox3VP16GR, specifically blocks tail formation when induced in tailbud stage embryos, comfirming the importance of Xhox3 for tail bud outgrowth in normal development. Grafts containing Notch ICD will only form tails if placed in the posterior part of the neural plate. However, if Xwnt3a is also present in the grafts they can form tails at any anteroposterior level. Since Xwnt3a expression is localised appropriately in the posterior at the time of tail bud formation it is likely to be responsible for restricting tail forming competence to the posterior neural plate in our assay. Combined expression of Xwnt3a and active Notch in animal cap explants is sufficient to induce Xhox3, provoke elongation and form neural tubes. Conservation of gene expression in the tail bud of other vertebrates suggests that this pathway may describe a general mechanism controlling tail outgrowth and secondary neurulation.

Properties of the primary organization field in the embryo of Xenopus laevis

Development ◽  
1972 ◽  
Vol 28 (1) ◽  
pp. 13-26
Author(s):  
J. Cooke
Keyword(s):  
Marginal Zone ◽  
Organizer Region ◽  
Angular Distance ◽  
Cell Polarization ◽  
Subsequent Paper ◽  
Basic Operation ◽  
Primary Organization ◽  
Organizer Activity ◽  
Set Up ◽  
Cell Immigration

The work presented, in this and the subsequent papers of a series, was begun in order to re-examine the properties of the amphibian primary embryonic field, in the light of current theories concerning the nature of individuation fields in developing animal systems. A detailed description is given of the basic operation whose results are described in this and the subsequent paper. This involves the transplantation, into a late blastula or stage-10 gastrula host, of a supernumerary stage-10 organizer region. The consequences of such operations during the following 4–6 h, up to the late gastrula stage, are also described. Evidence is presented that, from a time some 2·5 h before the organizer site first becomes externally visible, its presumptive region is immune from interference by the proximity of another, implanted organizer, even one which is itself 2·5 h older. That is to say, the final site of development of host organizer activity is not altered by the presence of such an implant. Pairs of early organizers at comparable stages of activity appear to set up competing fields of cellular orientation and immigration, which show a fairly sharp boundary at their interface. This is most obvious for pairs of organizers fairly close together, since the cell polarization and stretching is most pronounced in the region near to the apex of the field, i.e. the initial site of cell immigration. Independent initial fields of immigration due to two organizers can reliably be distinguished in cases where they are as little as 30° of angular distance apart in the marginal zone of the host. These results are to be considered in relation to those of Paper II, for the same series of operations, where the final patterns of cell differentiation are studied, and to those of Paper III, where evidence is given for the development of autonomous polarity in the region of the organizer.

Cngsc, a homologue of goosecoid, participates in the patterning of the head, and is expressed in the organizer region of Hydra

Development ◽  
1999 ◽  
Vol 126 (23) ◽  
pp. 5245-5254 ◽  
Author(s):  
M. Broun ◽  
S. Sokol ◽  
H.R. Bode
Keyword(s):  
Sensory Neurons ◽  
Organizer Region ◽  
Ventral Side ◽  
Evolutionary Conservation ◽  
The Body ◽  
Secondary Axis ◽  
Head Formation ◽  
Per Se ◽  
Endodermal Cells ◽  
Body Column

We have isolated Cngsc, a hydra homologue of goosecoid gene. The homeodomain of Cngsc is identical to the vertebrate (65-72%) and Drosophila (70%) orthologues. When injected into the ventral side of an early Xenopus embryo, Cngsc induces a partial secondary axis. During head formation, Cngsc expression appears prior to, and directly above, the zone where the tentacles will emerge, but is not observed nearby when the single apical tentacle is formed. This observation indicates that the expression of the gene is not necessary for the formation of a tentacle per se. Rather, it may be involved in defining the border between the hypostome and the tentacle zone. When Cngsc(+) tip of an early bud is grafted into the body column, it induces a secondary axis, while the adjacent Cngsc(−) region has much weaker inductive capacities. Thus, Cngsc is expressed in a tissue that acts as an organizer. Cngsc is also expressed in the sensory neurons of the tip of the hypostome and in the epithelial endodermal cells of the upper part of the body column. The plausible roles of Cngsc in organizer function, head formation and anterior neuron differentiation are similar to roles goosecoid plays in vertebrates and Drosophila. It suggests widespread evolutionary conservation of the function of the gene.

Differentiation of Ectoderm Implanted into the Primordium of the Limb Bud in the Amphibian Embryo and its Influence upon the Limb

1946 ◽  
Vol 22 (3-4) ◽  
pp. 101-106
Author(s):  
WALTER BRANDT
Keyword(s):  
Body Wall ◽  
Distal Part ◽  
The Body ◽  
Limb Bud ◽  
Muscle Fibres ◽  
Tail Bud ◽  
Amphibian Embryo ◽  
Microscopical Analysis ◽  
Proximal Half ◽  
Host Embryo

1. A microscopical analysis was made concerning the differentiation of ectoderm cut from the tip of the tail-bud of an amphibian embryo (Amblystoma mexicanum, stages 35-37, Harrison) after its implantation into the primordium of the limb-bud of a host embryo 3-5 weeks after operation. 2. The ectoderm which lay deep in the tissues of the limb differentiated either into solid epithelial cords or into cysts. 3. The ectoderm which was attached outside the limb differentiated into notched ectodermal elevations which included a mesenchymal core. 4. A microscopical analysis was made concerning the development of deformities of limbs as the result of the operation. 5. The scapula may be divided into isolated pieces, bundles of muscle fibres separating the pieces from each other. 6. A supernumerary piece of cartilage can develop close to the cartilage of the scapula. 7. The suprascapula may be absent and its place taken by a mass of muscle fibres. 8. A phocomelias may be produced when the whole length of the humerus and the elbow-joint lies inside the body wall. In this case the implanted ectoderm covers the area where the limb would normally develop. 9. The humerus may be reduplicated. 10. The humerus may be too short. 11. The proximal half of the humerus may possess a diameter different from that of the distal half. 12. One skeletal element only of the forearm (radius or ulna) may be present when the place which would normally be occupied by one of these elements was taken by implanted ectoderm. 13. The elements of the carpus and of the hand may appear irregularly scattered throughout the tissues of the distal part of the limb. In these cases the implanted ectoderm was attached to the surface of the distal end of the limb. 14. The fingers can show: (a) abnormal positions, (b) abnormal numbers, (c) syndactylias, (d) one finger too long, others too short.

The somitogenetic potential of cells in the primitive streak and the tail bud of the organogenesis-stage mouse embryo

Development ◽  
1992 ◽  
Vol 115 (3) ◽  
pp. 703-715 ◽  
Author(s):  
P.P. Tam ◽  
S.S. Tan
Keyword(s):  
Primitive Streak ◽  
Mouse Embryos ◽  
Paraxial Mesoderm ◽  
Tail Bud ◽  
Matrix Interaction ◽  
Cell Matrix ◽  
Age Related ◽  
Somite Formation ◽  
Lateral Mesoderm ◽  
Host Embryo

The developmental potency of cells isolated from the primitive streak and the tail bud of 8.5- to 13.5-day-old mouse embryos was examined by analyzing the pattern of tissue colonization after transplanting these cells to the primitive streak of 8.5-day embryos. Cells derived from these progenitor tissues contributed predominantly to tissues of the paraxial and lateral mesoderm. Cells isolated from older embryos could alter their segmental fate and participated in the formation of anterior somites after transplantation to the primitive streak of 8.5-day host embryo. There was, however, a developmental lag in the recruitment of the transplanted cells to the paraxial mesoderm and this lag increased with the extent of mismatch of developmental ages between donor and host embryos. It is postulated that certain forms of cell-cell or cell-matrix interaction are involved in the specification of segmental units and that there may be age-related variations in the interactive capability of the somitic progenitor cells during development. Tail bud mesenchyme isolated from 13.5-day embryos, in which somite formation will shortly cease, was still capable of somite formation after transplantation to 8.5-day embryos. The cessation of somite formation is therefore likely to result from a change in the tissue environment in the tail bud rather than a loss of cellular somitogenetic potency.

Positional information and pattern regulation in hydra: the effect of γ-radiation

Development ◽  
1973 ◽  
Vol 30 (3) ◽  
pp. 741-752
Author(s):  
J. Hicklin ◽  
L. Wolpert
Keyword(s):  
Cell Division ◽  
Positional Information ◽  
Γ Irradiation ◽  
Γ Radiation ◽  
Head Formation ◽  
High Doses ◽  
Mitotic Figures ◽  
Pattern Regulation

Hydra exposed to high doses of γ-irradiation (25000 rad) are still capable of regeneration although no normal mitotic figures could be seen for up to 48 h after irradiation. Irradiated heads could still inhibit head formation in other regions in graft combinations. The time for head end determination in irradiated animals appeared to be increased. It is concluded that head end regeneration need not involve cell division.

Characterization of the head organizer in hydra

Development ◽  
2002 ◽  
Vol 129 (4) ◽  
pp. 875-884 ◽  
Author(s):  
Mariya Broun ◽  
Hans R. Bode
Keyword(s):  
Organizer Region ◽  
Apical Part ◽  
The Body ◽  
Central Process ◽  
Axial Patterning ◽  
Secondary Axis ◽  
Head Formation ◽  
Body Column ◽  
Self Organizing

A central process in the maintenance of axial patterning in the adult hydra is the head activation gradient, i.e. the potential to form a secondary axis, which is maximal in the head and is graded down the body column. Earlier evidence suggested that this gradient was based on a single parameter. Using transplantation experiments, we provide evidence that the hypostome, the apical part of the head, has the characteristics of an organizer in that it has the capacity to induce host tissue to form most of the second axis. By contrast, tissue of the body column has a self-organizing capacity, but not an inductive capacity. That the inductive capacity is confined to the hypostome is supported by experiments involving a hypostome-contact graft. The hypostome, but not the body column, transmits a signal(s) leading to the formation of a second axis. In addition, variations of the transplantation grafts and hypostome-contact grafts provide evidence for several characteristics of the organizer. The inductive capacity of the head and the self-organizing capacity of the body column are based on different pathways. Head inhibition, yya signal produced in the head and transmitted to the body column to prevent head formation, represses the effect of the inducing signal by interfering with formation of the hypostome/organizer. These results indicate that the organizer characteristics of the hypostome of an adult hydra are similar to those of the organizer region of vertebrate embryos. They also indicate that the Gierer-Meinhardt model provides a reasonable framework for the mechanisms that underlie the organizer and its activities. In addition, the results suggest that a region of an embryo or adult with the characteristics of an organizer arose early in metazoan evolution.

Pattern formation along the anteroposterior axis of the chick wing: the increase in width following a polarizing region graft and the effect of X-irradiation

Development ◽  
1981 ◽  
Vol 63 (1) ◽  
pp. 127-144
Author(s):  
J. C. Smith ◽  
L. Wolpert
Keyword(s):  
Pattern Formation ◽  
Positional Information ◽  
Limb Bud ◽  
Anteroposterior Axis ◽  
X Irradiation ◽  
Host Embryo

A study is made of the widening of the chick limb bud that occurs after a graft of an additional polarizing region. Such buds are about 50% wider than controls, after 36 h. By contrast, growth along the proximodistal axis is unaffected. This widening is reduced by treating the host embryo with 10 Gy X-irradiation and the altered pattern of digits is consistent with a diffusible morphogen model for the specification of positional information along the anteroposterior axis.

Sign in / Sign up

Export Citation Format

Share Document