Anterior patterning by synergistic activity of the early gastrula organizer and the anterior germ layer tissues of the mouse embryo

Development ◽  
1999 ◽  
Vol 126 (22) ◽  
pp. 5171-5179 ◽  
Author(s):  
P.P. Tam ◽  
K.A. Steiner
Keyword(s):  
Primitive Streak ◽  
Germ Layer ◽  
Synergistic Activity ◽  
Visceral Endoderm ◽  
Neural Genes ◽  
Anterior Patterning ◽  
Host Embryo ◽  
Early Gastrula ◽  
Host Tissues ◽  
Anterior Visceral Endoderm

Fragments of the germ layer tissues isolated from the early-primitive-streak (early-streak) stage mouse embryos were tested for axis induction activity by transplantation to late-gastrula (late-streak to early-bud) stage host embryos. The posterior epiblast fragment that contains the early gastrula organizer was able to recruit the host tissues to form an ectopic axis. However, the most anterior neural gene that was expressed in the ectopic axis was Krox20 that marks parts of the hindbrain, but markers of the mid- and forebrain (Otx2 and En1) were not expressed. Anterior visceral endoderm or the anterior epiblast alone did not induce any ectopic neural tissue. However, when these two anterior germ layer tissues were transplanted together, they can induce the formation of ectopic host-derived neural tissues but these tissues rarely expressed anterior neural genes and did not show any organization of an ectopic axis. Therefore, although the anterior endoderm and epiblast together may display some inductive activity, they do not act like a classical organizer. Induction of the anterior neural genes in the ectopic axis was achieved only when a combination of the posterior epiblast fragment, anterior visceral endoderm and the anterior epiblast was transplanted to the host embryo. The formation of anterior neural structures therefore requires the synergistic interaction of the early gastrula organizer and anterior germ layer tissues.

scholarly journals Correct Patterning of the Primitive Streak Requires the Anterior Visceral Endoderm

PLoS ONE ◽  
2011 ◽  
Vol 6 (3) ◽  
pp. e17620 ◽  
Author(s):  
Daniel W. Stuckey ◽  
Aida Di Gregorio ◽  
Melanie Clements ◽  
Tristan A. Rodriguez
Keyword(s):  
Primitive Streak ◽  
Visceral Endoderm ◽  
Anterior Visceral Endoderm

The organizer of the mouse gastrula is composed of a dynamic population of progenitor cells for the axial mesoderm

Development ◽  
2001 ◽  
Vol 128 (18) ◽  
pp. 3623-3634 ◽  
Author(s):  
Simon J. Kinder ◽  
Tania E. Tsang ◽  
Maki Wakamiya ◽  
Hiroshi Sasaki ◽  
Richard R. Behringer ◽  
...  
Keyword(s):  
Primitive Streak ◽  
Cell Populations ◽  
Genetic Activity ◽  
Neural Axis ◽  
Prechordal Mesoderm ◽  
Stage Embryo ◽  
Dynamic Population ◽  
Host Embryo ◽  
Early Gastrula ◽  
Different Parts

An organizer population has been identified in the anterior end of the primitive streak of the mid-streak stage embryo, by the expression of Hnf3β, GsclacZ and Chrd, and the ability of these cells to induce a second neural axis in the host embryo. This cell population can therefore be regarded as the mid-gastrula organizer and, together with the early-gastrula organizer and the node, constitute the organizer of the mouse embryo at successive stages of development. The profile of genetic activity and the tissue contribution by cells in the organizer change during gastrulation, suggesting that the organizer may be populated by a succession of cell populations with different fates. Fine mapping of the epiblast in the posterior region of the early-streak stage embryo reveals that although the early-gastrula organizer contains cells that give rise to the axial mesoderm, the bulk of the progenitors of the head process and the notochord are localized outside the early gastrula organizer. In the mid-gastrula organizer, early gastrula organizer derived cells that are fated for the prechordal mesoderm are joined by the progenitors of the head process that are recruited from the epiblast previously anterior to the early gastrula organizer. Cells that are fated for the head process move anteriorly from the mid-gastrula organizer in a tight column along the midline of the embryo. Other mid-gastrula organizer cells join the expanding mesodermal layer and colonize the cranial and heart mesoderm. Progenitors of the trunk notochord that are localized in the anterior primitive streak of the mid-streak stage embryo are later incorporated into the node. The gastrula organizer is therefore composed of a constantly changing population of cells that are allocated to different parts of the axial mesoderm.

HNF3beta and Lim1 interact in the visceral endoderm to regulate primitive streak formation and anterior-posterior polarity in the mouse embryo

Development ◽  
1999 ◽  
Vol 126 (20) ◽  
pp. 4499-4511 ◽  
Author(s):  
A. Perea-Gomez ◽  
W. Shawlot ◽  
H. Sasaki ◽  
R.R. Behringer ◽  
S. Ang
Keyword(s):  
Mouse Embryo ◽  
Primitive Streak ◽  
Axis Formation ◽  
Visceral Endoderm ◽  
Primary Defect ◽  
Homozygous Mutant ◽  
Early Mouse ◽  
Mesoderm Patterning ◽  
Anterior Posterior ◽  
Anterior Visceral Endoderm

Recent embryological and genetic experiments have suggested that the anterior visceral endoderm and the anterior primitive streak of the early mouse gastrula function as head- and trunk-organising centers, respectively. Here, we report that HNF3beta and Lim1 are coexpressed in both organising centers suggesting synergistic roles of these genes in regulating organiser functions and hence axis development in the mouse embryo. To investigate this possibility, we generated compound HNF3beta and Lim1 mutant embryos. An enlarged primitive streak and a lack of axis formation were observed in HNF3beta (−)(/)(−);Lim1(−)(/)(−), but not in single homozygous mutant embryos. Chimera experiments indicate that the primary defect in these double homozygous mutants is due to loss of activity of HNF3beta and Lim1 in the visceral endoderm. Altogether, these data provide evidence that these genes function synergistically to regulate organiser activity of the anterior visceral endoderm. Moreover, HNF3beta (−)(/)(−);Lim1(−)(/)(−) mutant embryos also exhibit defects in mesoderm patterning that are likely due to lack of specification of anterior primitive streak cells.

Head induction in the chick by primitive endoderm of mammalian, but not avian origin

Development ◽  
1999 ◽  
Vol 126 (4) ◽  
pp. 815-825 ◽  
Author(s):  
H. Knoetgen ◽  
C. Viebahn ◽  
M. Kessel
Keyword(s):  
Lower Layer ◽  
Homeobox Gene ◽  
Primitive Streak ◽  
Neural Plate ◽  
Visceral Endoderm ◽  
Avian Origin ◽  
Bmp Antagonist ◽  
Rabbit Embryos ◽  
Inductive Potential ◽  
Anterior Visceral Endoderm

Different types of endoderm, including primitive, definitive and mesendoderm, play a role in the induction and patterning of the vertebrate head. We have studied the formation of the anterior neural plate in chick embryos using the homeobox gene GANF as a marker. GANF is first expressed after mesendoderm ingression from Hensen's node. We found that, after transplantation, neither the avian hypoblast nor the anterior definitive endoderm is capable of GANF induction, whereas the mesendoderm (young head process, prechordal plate) exhibits a strong inductive potential. GANF induction cannot be separated from the formation of a proper neural plate, which requires an intact lower layer and the presence of the prechordal mesendoderm. It is inhibited by BMP4 and promoted by the presence of the BMP antagonist Noggin. In order to investigate the inductive potential of the mammalian visceral endoderm, we used rabbit embryos which, in contrast to mouse embryos, allow the morphological recognition of the prospective anterior pole in the living, pre-primitive-streak embryo. The anterior visceral endoderm from such rabbit embryos induced neuralization and independent, ectopic GANF expression domains in the area pellucida or the area opaca of chick hosts. Thus, the signals for head induction reside in the anterior visceral endoderm of mammals whereas, in birds and amphibia, they reside in the prechordal mesendoderm, indicating a heterochronic shift of the head inductive capacity during the evolution of mammalia.

Otx2 is required for visceral endoderm movement and for the restriction of posterior signals in the epiblast of the mouse embryo

Development ◽  
2001 ◽  
Vol 128 (5) ◽  
pp. 753-765 ◽  
Author(s):  
A. Perea-Gomez ◽  
K.A. Lawson ◽  
M. Rhinn ◽  
L. Zakin ◽  
P. Brulet ◽  
...  
Keyword(s):  
Essential Role ◽  
Homeobox Gene ◽  
Primitive Streak ◽  
Lineage Tracing ◽  
Secreted Proteins ◽  
Visceral Endoderm ◽  
Cellular Mechanisms ◽  
Cell Fates ◽  
Marker Studies ◽  
Anterior Visceral Endoderm

Genetic and embryological experiments have demonstrated an essential role for the visceral endoderm in the formation of the forebrain; however, the precise molecular and cellular mechanisms of this requirement are poorly understood. We have performed lineage tracing in combination with molecular marker studies to follow morphogenetic movements and cell fates before and during gastrulation in embryos mutant for the homeobox gene Otx2. Our results show, first, that Otx2 is not required for proliferation of the visceral endoderm, but is essential for anteriorly directed morphogenetic movement. Second, molecules that are normally expressed in the anterior visceral endoderm, such as Lefty1 and Mdkk1, are not expressed in Otx2 mutants. These secreted proteins have been reported to antagonise, respectively, the activities of Nodal and Wnt signals, which have a role in regulating primitive streak formation. The visceral endoderm defects of the Otx2 mutants are associated with abnormal expression of primitive streak markers in the epiblast, suggesting that anterior epiblast cells acquire primitive streak characteristics. Taken together, our data support a model whereby Otx2 functions in the anterior visceral endoderm to influence the ability of the adjacent epiblast cells to differentiate into anterior neurectoderm, indirectly, by preventing them from coming under the influence of posterior signals that regulate primitive streak formation.

scholarly journals Characterisation of the transcriptional dynamics underpinning the function, fate, and migration of the mouse Anterior Visceral Endoderm

2021 ◽  
Author(s):  
Shifaan Thowfeequ ◽  
Jonathan Fiorentino ◽  
Di Hu ◽  
Maria Solovey ◽  
Sharon Ruane ◽  
...  
Keyword(s):  
Primitive Streak ◽  
Pharmacological Intervention ◽  
Visceral Endoderm ◽  
Migratory Behaviour ◽  
Tight Coupling ◽  
Transient Nature ◽  
Transcriptional Dynamics ◽  
And Migration ◽  
And Function ◽  
Anterior Visceral Endoderm

During early post-implantation development of the mouse embryo, the Anterior Visceral Endoderm (AVE) differs from surrounding visceral endoderm (VE) in its migratory behaviour and ability to restrict primitive streak formation to the opposite side of the egg cylinder. In order to characterise the molecular basis for the unique properties of the AVE, we combined single-cell RNA-sequencing of the VE prior to and during AVE migration, with high-resolution imaging, short-term lineage labelling, phosphoproteomics and pharmacological intervention. This revealed the transient nature of the AVE, the emergence of heterogeneities in AVE transcriptional states relative to position of cells, and its prominence in establishing gene expression asymmetries within the spatial constraints of the embryo. We identified a previously unknown requirement of Ephrin- and Semaphorin-signalling for AVE migration. These findings point to a tight coupling of transcriptional state and position in the AVE and reveal molecular heterogeneities underpinning its migratory behaviour and function.

Studies on self-differentiating and induction capacities of Hensen's node using intracoelomic grafting technique

Development ◽  
1972 ◽  
Vol 28 (3) ◽  
pp. 547-558
Author(s):  
J. R. Viswanath ◽  
Leela Mulherkar
Keyword(s):  
Chick Embryo ◽  
Neural Tissue ◽  
Primitive Streak ◽  
Germ Layer ◽  
Grafting Technique ◽  
Definite Combination

Living Hensen's node of the definitive primitive streak of chick embryo was prepared into ‘sandwiches’ with the competent ectoderm and the sandwich grafts were transplated into the 2·5 day chick embryo using the intracoelomic grafting technique of Hamburger. One hundred and twenty-four grafts were prepared and transplanted intracoelomically, 28 grafts were lost due to the death of the host embryos, 63 grafts did not differentiate at all, but 33 well-defined grafts were recovered, after cultivating the transplanted hosts for 12–14 days. All kinds of tissues from feather germs to neural tissue were found to have differentiated in the grafts. The more frequently occurring tissues were feather germs, epidermal vesicle, neural tissue, kidney and muscle. Other differentiations were the cartilage notochord and gut. No definite combination pattern has emerged from the tissues. But when the tissues were traced to their germ-layer derivation, 22 of them belonged to the mesodermal complex, 11 to the ectodermal complex and 8 to the endodermal complex. In the light of the above results, the probable existence of a mesodermal factor and an ectodermal factor independently responsible for the respective differentiations, as also the competence of the ectoderm, is discussed.

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