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Letter
Nature Genetics  36, 293 - 297 (2004)
Published online: 15 February 2004; | doi:10.1038/ng1308

A conserved developmental program for sensory organ formation in Drosophila melanogaster

Nao Niwa1, 4, Yasushi Hiromi1, 2, 3 & Masataka Okabe1, 2, 5

1  Division of Developmental Genetics, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.

2  Department of Genetics, SOKENDAI, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.

3  CREST, Japan Science and Technology Agency, Japan.

4  Present addresses: Morphogenetic Signaling group, RIKEN Center for Developmental Biology, 2-2-3 Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.

5  Present addresses: MRC Centre for Developmental Neurobiology, King's College London, New Hunt's House, 4th Floor, Guy's Hospital Campus, London SE1 1UL, UK.

Correspondence should be addressed to Yasushi Hiromi yhiromi@lab.nig.ac.jp or Masataka Okabe maokabe@lab.nig.ac.jp
Different sensory organs, such the eye and ear, are widely thought to have separate origins, guided by distinct organ-specific factors that direct all aspects of their development. Previous studies of the D. melanogaster gene eyeless (ey) and its vertebrate homolog Pax6 suggested that this gene acts in such a manner and specifically drives eye development1, 2. But diverse sensory organs might instead arise by segment-specific modification of a developmental program that is involved more generally in sensory organ formation. In D. melanogaster, a common proneural gene called atonal (ato) functions in the initial process of development of a number of segment-specific organs, including the compound eye, the auditory organ and the stretch receptor3, 4, suggesting that these organs share an evolutionary origin. Here we show that D. melanogaster segment-specific sensory organs form through the integration of decapentaplegic (dpp), wingless (wg) and ecdysone signals into a single cis-regulatory element of ato. The induction of ectopic eyes by ey also depends on these signals for ato expression, and the ey mutant eye imaginal disc allows ato expression if cell death is blocked. These results imply that ey does not induce the entire eye morphogenetic program but rather modifies ato-dependent neuronal development. Our findings strongly suggest that various sensory organs evolved from an ato-dependent protosensory organ through segment specification by ey and Hox genes.


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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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