fork head gene
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2002 ◽  
Vol 118 (1-2) ◽  
pp. 161-163 ◽  
Author(s):  
Carla Tribioli ◽  
Raymond F Robledo ◽  
Thomas Lufkin
Keyword(s):  

Development ◽  
2000 ◽  
Vol 127 (1) ◽  
pp. 187-195 ◽  
Author(s):  
K. Yasui ◽  
S. Zhang ◽  
M. Uemura ◽  
H. Saiga

The long-standing question of how asymmetric development or asymmetric body structures in lancelets (amphioxus) are phylogenetically related to the body plan of other animals is still untouched. Three anterior structures, the preoral pit, club-shaped gland and mouth, are remarkable asymmetric features in developing lancelets that all open on the left side of the body. A Ptx-related gene, BbPtx is the first identified transcription factor gene with an asymmetrical expression pattern in lancelets similar to that in vertebrates, and thus it may provide a clue for the above question. Expression of the BbPtx gene is first detected at the dorsal margin of the blastopore in early mid-gastrulae and then becomes restricted to the left anterodorsal wall of the primitive gut and to the developing left somitocoelomic system. Expression continues on the left side in the developing preoral pit, club-shaped gland and mouth as well as in the mesoderm at the caudal end. Unlike D-Ptx1 in Drosophila, BbPtx is not coexpressed with a fork head gene in lancelets; instead the two genes are expressed in a complementary fashion on the left side of the embryo. The expression pattern of BbPtx is not compatible with the calcichordate hypothesis of Jefferies, in which the proposed ancestor of chordates rotated its tail 90 degrees counterclockwise in relation to the head/trunk. The expression of both BbPtx and vertebrate Pitx2 in tissues derived from the coelom implies that the left-right asymmetric development has a common origin between cephalochordates and vertebrates. Considering the development of the coelom in deuterostomes, however, left-right asymmetric development involving Pitx2-related genes is rather likely to be a primitive character shared among deuterostomes.


Development ◽  
1999 ◽  
Vol 126 (22) ◽  
pp. 5107-5116
Author(s):  
K.L. Kenyon ◽  
S.A. Moody ◽  
M. Jamrich

Xlens1 is a novel Xenopus member of the fork head gene family, named for its nearly restricted expression in the anterior ectodermal placode, presumptive lens ectoderm (PLE), and anterior epithelium of the differentiated lens. The temporal and spatial restriction of its expression suggests that: (1) Xlens1 is transcribed initially at neural plate stages in response to putative signals from the anterior neural plate that transform lens-competent ectoderm to lens-biased ectoderm; (2) further steps in the process of lens-forming bias restrict Xlens1 expression to the presumptive lens ectoderm (PLE) during later neural plate stages; (3) interactions with the optic vesicle maintain Xlens1 expression in the lens placode; and (4) Xlens1 expression is downregulated as committed lens cells undergo terminal differentiation. Induction assays demonstrate that pax6 induces Xlens1 expression, but unlike pax6, Xlens1 cannot induce the expression of the lens differentiation marker beta-crystallin. In the whole embryo, overexpression of Xlens1 in the lens ectoderm causes it to thicken and maintain gene expression characteristics of the PLE. Also, this overexpression suppresses differentiation in the lens ectoderm, suggesting that Xlens1 functions to maintain specified lens ectoderm in an undifferentiated state. Misexpression of Xlens1 in other regions causes hypertrophy of restricted tissues but only occasionally leads ectopic sites of gamma-crystallin protein expression in select anterior head regions. These results indicate that Xlens1 expression alone does not specify lens ectoderm. Lens specification and differentiation likely depends on a combination of other gene products and an appropriate level of Xlens1 activity.


Genomics ◽  
1997 ◽  
Vol 40 (3) ◽  
pp. 462-469 ◽  
Author(s):  
Derek B. Murphy ◽  
Stefanie Seemann ◽  
Stefan Wiese ◽  
Renate Kirschner ◽  
Karl H. Grzeschik ◽  
...  

Author(s):  
Stefan Wiese ◽  
Derek B. Murphy ◽  
Astrid Schlung ◽  
Peter Burfeind ◽  
Daphne Schmundt ◽  
...  

Genomics ◽  
1994 ◽  
Vol 21 (3) ◽  
pp. 551-557 ◽  
Author(s):  
Derek B. Murphy ◽  
Stefan Wiese ◽  
Peter Burfeind ◽  
Daphne Schmundt ◽  
Marie-Genevieve Mattei ◽  
...  

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