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Two Medfly Promoters That Have Originated by Recent Gene Duplication Drive Distinct Sex, Tissue and Temporal Expression Patterns
George K. Christophidesa, Ioannis Livadarasb, Charalambos Savakisb, and Katia Komitopoulouaa Department of Genetics and Biotechnology, School of Biological Sciences, University of Athens, Panepistimiopolis, Athens 157 01, Greece
b Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Heraklion 711 10, Crete, Greece
Corresponding author: Katia Komitopoulou, Department of Genetics and Biotechnology, School of Biological Sciences, University of Athens, Panepistimiopolis, Athens 15701, Greece., akomitop{at}biology.db.uoa.gr (E-mail)
Communicating editor: A. J. LOPEZ
2 and MSSP-ß2, overlapping fragments of their promoters, containing the 5' UTRs and 5' flanking regions, were fused to the lacZ reporter gene and introduced into the medfly genome via Minos-mediated germline transformation. Transgenic flies were functionally assayed for ß-galactosidase activity. Despite their extensive sequence similarity, the two gene promoters show distinct expression patterns of the reporter gene, consistent with previously reported evidence for analogous transcriptional activity of the corresponding endogenous genes. The MSSP-
2 promoter drives gene expression specifically in the fat body of the adult males, whereas the MSSP-ß2 promoter directs gene expression in the midgut of both sexes. In contrast, similar transformation experiments in Drosophila melanogaster showed that both promoters drive the expression of the reporter gene in the midgut of adult flies of both sexes. Thus, the very same MSSP-
2 promoter fragment directs expression in the adult male fat body in Ceratitis, but in the midgut of both sexes in Drosophila. Our data suggest that through the evolution of the MSSP gene family a limited number of mutations that occurred within certain cis-acting elements, in combination with new medfly-specific trans-acting factors, endowed these recently duplicated genes with distinct sex-, tissue-, and temporal-specific expression patterns.
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