MicroRNA-9 directs late organizer activity of the midbrain-hindbrain boundary

2008 ◽  
Vol 11 (6) ◽  
pp. 641-648 ◽  
Author(s):  
Christoph Leucht ◽  
Christian Stigloher ◽  
Andrea Wizenmann ◽  
Ruth Klafke ◽  
Anja Folchert ◽  
...  
Keyword(s):  
Development ◽  
2000 ◽  
Vol 127 (16) ◽  
pp. 3407-3417 ◽  
Author(s):  
L. Saude ◽  
K. Woolley ◽  
P. Martin ◽  
W. Driever ◽  
D.L. Stemple

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.


Development ◽  
1993 ◽  
Vol 119 (4) ◽  
pp. 991-1004 ◽  
Author(s):  
L.K. Gont ◽  
H. Steinbeisser ◽  
B. Blumberg ◽  
E.M. de Robertis

Three lines of evidence suggest that tail formation in Xenopus is a direct continuation of events initiated during gastrulation. First, the expression of two gene markers, Xbra and Xnot2, can be followed from the blastopore lip into distinct cell populations of the developing tailbud. Second, the tip of the tail retains Spemann's tail organizer activity until late stages of development. Third, lineage studies with the tracer DiI indicate that the cells of the late blastopore are fated to form specific tissues of the tailbud, and that intercalation of dorsal cells continues during tail elongation. In particular, the fate map shows that the tip of the tail is a direct descendant of the late dorsal blastopore lip. Thus, the tailbud is not an undifferentiated blastema as previously thought, but rather consists of distinct cell populations which arise during gastrulation.


Development ◽  
1972 ◽  
Vol 28 (1) ◽  
pp. 13-26
Author(s):  
J. Cooke

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.


Chromosoma ◽  
1984 ◽  
Vol 89 (5) ◽  
pp. 370-376 ◽  
Author(s):  
M. C. Cerme�o ◽  
J. Orellana ◽  
J. L. Santos ◽  
J. R. Lacadena

In chick blastoderms at primitive streak stage, lengths of the primitive streak were cut out and replaced with their antero-posterior orientation reversed. In some experiments the region immediately in front of the primitive streak (presumptive prechordal head) was also included in the excisedpiece. Control operations involving excision and replacement without reversal were also performed. The embryos were subsequently grown in vitro by Waddington’s technique. After reversal of a variety of different parts of the streak at various developmental stages, many cases of regulative development were obtained. In these, the original orientation of the blastoderm was maintained, and while there were abnormalities of various kinds in the embryos, they were no different from the abnormalities found in the controls. Very occasionally the regulated axis was partially doubled after a reversal, though not after a control operation. A few specimens which had undergone reversal of long pieces of the primitive streak and had completely healed showed a failure of regulation in that there was some tendency for the reversed-piece to develop according to its own orientation. But at best this reversed differentiation was very distorted and incomplete. Evidently the orientation of the primitive streak does not at any stage control the orientation of the embryo; and the primitive streak, when it is fully developed and contains most of the presumptive axial material, is highly labile in its powers of differentiation. In spite of its well-known ‘organizer' activity, the primitive streak is subject to control by the surrounding blastoderm.


2008 ◽  
Vol 19 (3) ◽  
pp. 145-148 ◽  
Author(s):  
D. M. Cheng ◽  
T. E. Denton ◽  
S. L. Liem ◽  
C. L. Elliot

1986 ◽  
Vol 28 (2) ◽  
pp. 227-234 ◽  
Author(s):  
N. Cuñado ◽  
M. C. Cermeño ◽  
J. Orellana

Nucleoli and nucleolar organizer regions (NORs) have been studied by a silver staining method in all meiotic stages of wheat–rye hybrid plants. The maximum number of nucleoli per cell scored at meiotic prophase and tapetum binucleate cells indicates that only the NORs of 1B, 6B, and 5D wheat chromosomes are active, whereas that of chromosome IR (SAT) of rye is inactive. However, at diakinesis, metaphase and anaphase meiotic stages only chromosomes 1B and 6B show Ag-NOR as was reported previously in somatic metaphase. The absence of Ag-NOR on chromosome 5D has been imputed to its low nucleolar organizer activity, not detectable by silver staining, because of the small number of rDNA clusters it carries. On the other hand, the meiotic behaviour of chromosomes 1B and 6B has been studied at metaphase I and anaphase I, using the Ag-NORs as cytological markers.Key words: nucleolar organizer, Ag-NOR, meiosis, wheat–rye hybrids.


1989 ◽  
Vol 30 (3) ◽  
pp. 164-173 ◽  
Author(s):  
K. C. Arden ◽  
D. A. Johnston ◽  
A. Cork ◽  
S. Pathak

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