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Developmental rescue ofDrosophilacephalic defects by the humanOtxgenes
Author(s) -
Tomoko Nagao,
Sandra Leuzinger,
Dario Acampora,
Antonio Simeone,
Robert Finkelstein,
Heinrich Reichert,
Katsuo Furukubo-Tokunaga
Publication year - 1998
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.95.7.3737
Subject(s) - biology , body plan , homeobox , vertebrate , gene , drosophila melanogaster , genetics , developmental biology , drosophila (subgenus) , bilateria , drosophilidae , evolutionary biology , microbiology and biotechnology , transcription factor , phylogenetics
The molecular mechanisms of head development are a central question in vertebrate and invertebrate developmental biology. The anteriorly expressed homeobox gene otd in Drosophila and its homolog Otx in mouse are required for the early development of the most anterior part of the body, suggesting that a fundamental genetic program of cephalic development might be conserved between vertebrates and invertebrates. We have examined this hypothesis by introducing the human Otx genes into flies. By inducing expression of the human Otx homologs with a heat shock promoter, we found that both Otx1 and Otx2 functionally complement the cephalic defects of a fly otd mutant through specific activation and inactivation of downstream genes. Combined with previous morphological studies, these results are consistent with the view that a common molecular ground plan of cephalization was invented before the diversification of the protostome and the deuterostome in the course of metazoan evolution.

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