scholarly journals Regionalised signalling within the extraembryonic ectoderm regulates anterior visceral endoderm positioning in the mouse embryo

2006 ◽  
Vol 123 (4) ◽  
pp. 288-296 ◽  
Author(s):  
Lucy Richardson ◽  
Maria-Elena Torres-Padilla ◽  
Magdalena Zernicka-Goetz
Keyword(s):  
Mouse Embryo ◽  
Visceral Endoderm ◽  
Anterior Visceral Endoderm

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.

scholarly journals The anterior visceral endoderm of the mouse embryo is established from both preimplantation precursor cells and by de novo gene expression after implantation

2007 ◽  
Vol 309 (1) ◽  
pp. 97-112 ◽  
Author(s):  
Maria-Elena Torres-Padilla ◽  
Lucy Richardson ◽  
Paulina Kolasinska ◽  
Sigolène M. Meilhac ◽  
Merlin Verena Luetke-Eversloh ◽  
...  
Keyword(s):  
Gene Expression ◽  
Mouse Embryo ◽  
De Novo ◽  
Precursor Cells ◽  
Visceral Endoderm ◽  
De Novo Gene ◽  
Anterior Visceral Endoderm

scholarly journals Heading forwards: anterior visceral endoderm migration in patterning the mouse embryo

2014 ◽  
Vol 369 (1657) ◽  
pp. 20130546 ◽  
Author(s):  
Matthew J. Stower ◽  
Shankar Srinivas
Keyword(s):  
Epithelial Cells ◽  
Early Development ◽  
Mouse Embryo ◽  
Visceral Endoderm ◽  
Coordinated Action ◽  
Specialized Population ◽  
The Brain ◽  
Anterior Posterior ◽  
Anterior Visceral Endoderm

The elaboration of anterior–posterior (A–P) pattern is one of the earliest events during development and requires the precisely coordinated action of several players at the level of molecules, cells and tissues. In mammals, it is controlled by a specialized population of migratory extraembryonic epithelial cells, the anterior visceral endoderm (AVE). The AVE is a signalling centre that is responsible for several important patterning events during early development, including specifying the orientation of the A–P axis and the position of the heart with respect to the brain. AVE cells undergo a characteristic stereotypical migration which is crucial to their functions.

scholarly journals β-Pix directs collective migration of anterior visceral endoderm cells in the early mouse embryo

2014 ◽  
Vol 28 (24) ◽  
pp. 2764-2777 ◽  
Author(s):  
Tatiana Omelchenko ◽  
M. Angeles Rabadan ◽  
Rocío Hernández-Martínez ◽  
Joaquim Grego-Bessa ◽  
Kathryn V. Anderson ◽  
...  
Keyword(s):  
Mouse Embryo ◽  
Visceral Endoderm ◽  
Collective Migration ◽  
Early Mouse Embryo ◽  
Early Mouse ◽  
Anterior Visceral Endoderm

The Foxh1-dependent autoregulatory enhancer controls the level of Nodal signals in the mouse embryo

Development ◽  
2002 ◽  
Vol 129 (14) ◽  
pp. 3455-3468 ◽  
Author(s):  
Dominic P. Norris ◽  
Jane Brennan ◽  
Elizabeth K. Bikoff ◽  
Elizabeth J. Robertson
Keyword(s):  
Mouse Embryo ◽  
Late Onset ◽  
Axis Formation ◽  
Visceral Endoderm ◽  
Mouse Development ◽  
Developmental Abnormalities ◽  
Intronic Enhancer ◽  
Vertebrate Embryo ◽  
Early Mouse ◽  
Pitx2 Expression

The TGFβ-related growth factor Nodal governs anteroposterior (AP) and left-right (LR) axis formation in the vertebrate embryo. A conserved intronic enhancer (ASE), containing binding sites for the fork head transcription factor Foxh1, modulates dynamic patterns of Nodal expression during early mouse development. This enhancer is responsible for early activation of Nodal expression in the epiblast and visceral endoderm, and at later stages governs asymmetric expression during LR axis formation. We demonstrate ASE activity is strictly Foxh1 dependent. Loss of this autoregulatory enhancer eliminates transcription in the visceral endoderm and decreases Nodal expression in the epiblast, but causes surprisingly discrete developmental abnormalities. Thus lowering the level of Nodal signaling in the epiblast disrupts both orientation of the AP axis and specification of the definitive endoderm. Targeted removal of the ASE also dramatically reduces left-sided Nodal expression, but the early events controlling LR axis specification are correctly initiated. However loss of the ASE disrupts Lefty2 (Leftb) expression and causes delayed Pitx2 expression leading to late onset, relatively minor LR patterning defects. The feedback loop is thus essential for maintenance of Nodal signals that selectively regulate target gene expression in a temporally and spatially controlled fashion in the mouse embryo.

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