Genetics, Vol. 166, 1833-1843, April 2004, Copyright © 2004

Molecular and Functional Analysis of scalloped Recessive Lethal Alleles in Drosophila melanogaster

Ajay Srivastavaa, Andrew J. Simmondsb, Ankush Garga, Leif Fossheimb, Shelagh D. Campbella, and John B. Bella
a Department of Biological Sciences, University of Alberta, Edmonton, Alberta T6G 2E9, Canada
b Department of Cell Biology, University of Alberta, Edmonton, Alberta T6G 2E9, Canada

Corresponding author: John B. Bell, University of Alberta, Edmonton, AB T6G 2E9, Canada., jbell{at}ualberta.ca (E-mail)

Communicating editor: T. SCHÜPBACH

The Drosophila melanogaster scalloped (sd) gene is a homolog of the human TEF-1 gene and is a member of the TEA/ATTS domain-containing family of transcription factors. In Drosophila, sd is involved in wing development as well as neural development. Herein, data are presented from a molecular analysis of five recessive lethal sd alleles. Only one of these alleles complements a viable allele associated with an sd mutant wing phenotype, suggesting that functions important for wing development are compromised by the noncomplementing alleles. Two of the wing noncomplementing alleles have mutations that help to define a VG-binding domain for the SD protein in vivo, and another noncomplementing allele has a lesion within the TEA DNA-binding domain. The VG-binding domain overlaps with a domain important for viability of the fly, since two of the sd lethal lesions are located there. The fifth lethal affects a yet undefined motif lying just outside the VG-binding domain in the C-terminal direction that affects both wing phenotype and viability. This is the first example linking mutations affecting specific amino acids in the SD protein with phenotypic consequences for the organism.





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