Faculty Opinions recommendation of Dynamic changes in the response of cells to positive hedgehog signaling during mouse limb patterning.

Author(s):  
Ed Laufer
2007 ◽  
Vol 1116 (1) ◽  
pp. 100-112 ◽  
Author(s):  
E. KOYAMA ◽  
T. OCHIAI ◽  
R. B. ROUNTREE ◽  
D. M. KINGSLEY ◽  
M. ENOMOTO-IWAMOTO ◽  
...  

2020 ◽  
Vol 8 (4) ◽  
pp. 31
Author(s):  
Ines Desanlis ◽  
Rachel Paul ◽  
Marie Kmita

Limb patterning relies in large part on the function of the Hox family of developmental genes. While the differential expression of Hox genes shifts from the anterior–posterior (A–P) to the proximal–distal (P–D) axis around embryonic day 11 (E11), whether this shift coincides with a more global change of A–P to P–D patterning program remains unclear. By performing and analyzing the transcriptome of the developing limb bud from E10.5 to E12.5, at single-cell resolution, we have uncovered transcriptional trajectories that revealed a general switch from A–P to P–D genetic program between E10.5 and E11.5. Interestingly, all the transcriptional trajectories at E10.5 end with cells expressing either proximal or distal markers suggesting a progressive acquisition of P–D identity. Moreover, we identified three categories of genes expressed in the distal limb mesenchyme characterized by distinct temporal expression dynamics. Among these are Hoxa13 and Hoxd13 (Hox13 hereafter), which start to be expressed around E10.5, and importantly the binding of the HOX13 factors was observed within or in the neighborhood of several of the distal limb genes. Our data are consistent with previous evidence suggesting that the transition from the early/proximal to the late/distal transcriptome of the limb mesenchyme largely relies on HOX13 function. Based on these results and the evidence that HOX13 factors restrict Hoxa11 expression to the proximal limb, in progenitor cells of the zeugopod, we propose that HOX13 act as a key determinant of P–D patterning.


2000 ◽  
Vol 57 (12) ◽  
pp. 1682-1694 ◽  
Author(s):  
J. Capdevila* ◽  
R. L. Johnson

Science ◽  
2009 ◽  
Vol 323 (5917) ◽  
pp. 1050-1053 ◽  
Author(s):  
J.-D. Benazet ◽  
M. Bischofberger ◽  
E. Tiecke ◽  
A. Goncalves ◽  
J. F. Martin ◽  
...  

2008 ◽  
Vol 8 (1) ◽  
pp. 83 ◽  
Author(s):  
April DeLaurier ◽  
Nicholas Burton ◽  
Michael Bennett ◽  
Richard Baldock ◽  
Duncan Davidson ◽  
...  

2009 ◽  
Vol 238 (12) ◽  
pp. 3175-3184 ◽  
Author(s):  
Liam Town ◽  
Edwina McGlinn ◽  
Salvatore Fiorenza ◽  
Vicki Metzis ◽  
Natalie C. Butterfield ◽  
...  

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Rachel K Lex ◽  
Zhicheng Ji ◽  
Kristin N Falkenstein ◽  
Weiqiang Zhou ◽  
Joanna L Henry ◽  
...  

Transcriptional repression needs to be rapidly reversible during embryonic development. This extends to the Hedgehog pathway, which primarily serves to counter GLI repression by processing GLI proteins into transcriptional activators. In investigating the mechanisms underlying GLI repression, we find that a subset of GLI binding regions, termed HH-responsive enhancers, specifically loses acetylation in the absence of HH signaling. These regions are highly enriched around HH target genes and primarily drive HH-specific transcriptional activity in the mouse limb bud. They also retain H3K27ac enrichment in limb buds devoid of GLI activator and repressor, indicating that their activity is primarily regulated by GLI repression. Furthermore, the Polycomb repression complex is not active at most of these regions, suggesting it is not a major mechanism of GLI repression. We propose a model for tissue-specific enhancer activity in which an HDAC-associated GLI repression complex regulates target genes by altering the acetylation status at enhancers.


Author(s):  
Jean-Denis Benazet ◽  
Mirko Bischofberger ◽  
Eva Tiecke ◽  
Alexandre Gonalves ◽  
James F. Martin ◽  
...  

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