Reference Report
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| Citation | Tio, M., Ma, C., Moses, K. (1994). spitz, a Drosophila homolog of transforming growth factor-, is required in the founding photoreceptor cells of the compound eye facets. Mech. Dev. 48(1): 13--23. (Export to RIS) | ||
| FlyBase ID | FBrf0079521 | ||
| Publication Type | Research paper | ||
| PubMed ID | 7833285 | ||
| PubMed Abstract | Cell type specification and differentiation in the developing Drosophila compound eye begins in the morphogenetic furrow. In the furrow, cells are organized into evenly spaced preclusters and there is a synchronized arrest of the cells' mitotic cycle in G1. We report that recessive spitz loss-of-function mutations affect compound eye development. Spitz is homologous to the human transforming growth factor-alpha. In mosaic clones, spitz function is required in the first photoreceptor cells to differentiate for normal ommatidial development. spitz loss-of-function mutations are dominant suppressors of EgfrE gain-of-function mutations of the epidermal growth factor-receptor gene. These data suggest that the spitz product is a precluster promoting factor. spitz transcription increases abruptly in the morphogenetic furrow, the obverse of Egfr expression. We present a model for the expression of, and cellular requirement for, this growth factor homolog. | ||
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| Language of Publication | English | ||
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| Publication Type | Journal | ||
| Abbreviation | Mech. Dev. | ||
| Title | Mechanisms of Development | ||
| Publication Year | 1990- | ||
| ISBN/ISSN | 0925-4773 | ||
Data from Reference
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Aberrations (6)
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Alleles (12)
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Genes (6)
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Insertions (2)
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