feather buds
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2016 ◽  
Vol 110 (3) ◽  
pp. 258a
Author(s):  
Ang Li ◽  
Jung-Hwa Cho ◽  
Brian Reid ◽  
Min Zhao ◽  
Robert H. Chow ◽  
...  

2010 ◽  
Vol 6 (4) ◽  
pp. 517-520 ◽  
Author(s):  
Masayoshi Tokita ◽  
Noriko Iwai

Frogs have highly conserved hand and foot morphology, possessing four fingers and five toes. As an exception, two Japanese ranid frog species, the Otton frog Babina subaspera and the dagger frog Babina holsti , possess a unique thumb-like structure (the pseudothumb) in the forelimb, giving an appearance of a total of five fingers on the hand. To obtain insights into the developmental mechanisms that generate this novel character, we investigated the hand morphogenesis of the Otton frog. The unique morphological pattern of the pseudothumb was already established in juveniles. Surprisingly, the bud-like structure, which is similar to the area of inductive activity (e.g. feather buds in birds and the carapacial ridge in turtles), was detected over the site where the future prepollex develops in larvae. By contrast, this bud-like structure was not found in larvae of other ranid species. We discuss possible scenarios that would favour the evolution of this very unusual trait in frogs.


2005 ◽  
Vol 73 (5) ◽  
pp. 240-248 ◽  
Author(s):  
Jae-Young Kim ◽  
Sung-Won Cho ◽  
Wu-Chul Song ◽  
Min-Jung Lee ◽  
Jinglei Cai ◽  
...  
Keyword(s):  

2004 ◽  
Vol 272 (1) ◽  
pp. 76-88 ◽  
Author(s):  
Iain W McKinnell ◽  
Mark Turmaine ◽  
Ketan Patel
Keyword(s):  

2004 ◽  
Vol 270 (1) ◽  
pp. 94-105 ◽  
Author(s):  
Iain W McKinnell ◽  
Helen Makarenkova ◽  
Ivan de Curtis ◽  
Mark Turmaine ◽  
Ketan Patel

Gene ◽  
2001 ◽  
Vol 271 (2) ◽  
pp. 151-158 ◽  
Author(s):  
Jane E Olsson ◽  
Yusuke Kamachi ◽  
Sarah Penning ◽  
George E.O Muscat ◽  
Hisato Kondoh ◽  
...  
Keyword(s):  

2000 ◽  
Vol 219 (1) ◽  
pp. 98-114 ◽  
Author(s):  
Randall B. Widelitz ◽  
Ting-Xin Jiang ◽  
Jianfen Lu ◽  
Cheng-Ming Chuong

Development ◽  
1999 ◽  
Vol 126 (12) ◽  
pp. 2577-2587 ◽  
Author(s):  
R.B. Widelitz ◽  
T.X. Jiang ◽  
C.W. Chen ◽  
N.S. Stott ◽  
C.M. Chuong

How do vertebrate epithelial appendages form from the flat epithelia? Following the formation of feather placodes, the previously radially symmetrical primordia become anterior-posterior (A-P) asymmetrical and develop a proximo-distal (P-D) axis. Analysis of the molecular heterogeneity revealed a surprising parallel of molecular profiles in the A-P feather buds and the ventral-dorsal (V-D) Drosophila appendage imaginal discs. The functional significance was tested with an in vitro feather reconstitution model. Wnt-7a expression initiated all over the feather tract epithelium, intensifying as it became restricted first to the primordia domain, then to an accentuated ring pattern within the primordia border, and finally to the posterior bud. In contrast, sonic hedgehog expression was induced later as a dot within the primordia. RCAS was used to overexpress Wnt-7a in reconstituted feather explants derived from stage 29 dorsal skin to further test its function in feather formation. Control skin formed normal elongated, slender buds with A-P orientation, but Wnt-7a overexpression led to plateau-like skin appendages lacking an A-P axis. Feathers in the Wnt-7a overexpressing skin also had inhibited elongation of the P-D axes. This was not due to a lack of cell proliferation, which actually was increased although randomly distributed. While morphogenesis was perturbed, differentiation proceeded as indicated by the formation of barb ridges. Wnt-7a buds have reduced expression of anterior (Tenascin) bud markers. Middle (Notch-1) and posterior bud markers including Delta-1 and Serrate-1 were diffusely expressed. The results showed that ectopic Wnt-7a expression enhanced properties characteristic of the middle and posterior feather buds and suggest that P-D elongation of vertebrate skin appendages requires balanced interactions between the anterior and posterior buds.


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