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An essential component of normal development is controlling the transition from cell proliferation to differentiation. One such transition occurs during Drosophila oogenesis. In early oogenesis, germ cells undergo mitotic proliferation and contain a specialized organelle called a fusome, whereas later post-mitotic cells differentiate and lose the fusome as F-actin-rich ring canals form. The hts gene encodes the only Drosophila Adducin, and is a female-sterile mutant that affects both the fusome and ring canals. We show that one Hts protein, Ovhts, is a polyprotein that is cleaved to produce two products, Ovhts-Fus and Ovhts-RC. Whereas Ovhts-Fus localizes to the fusome in mitotic cells, Ovhts-RC localizes to ring canals throughout later oogenesis. We demonstrate that an uncleavable version of Ovhts delays the transition from fusome-containing cells to those that have ring canals. Ovhts is the first polyprotein shown to produce proteins that function in separate structures.
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Development ePress online publication date 10 Jan 2007
doi: 10.1242/dev.02766
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The Ovhts polyprotein is cleaved to produce fusome and ring canal proteins required for Drosophila oogenesis
* Author for correspondence (e-mail: lynn.cooley{at}yale.edu)
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S. Aruna, H. A. Flores, and D. A. Barbash
Reduced Fertility of Drosophila melanogaster Hybrid male rescue (Hmr) Mutant Females Is Partially Complemented by Hmr Orthologs From Sibling Species
Genetics,
April 1, 2009;
181(4):
1437 - 1450.
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© The Company of Biologists Ltd 2007