Castor is required for Hedgehog-dependent cell-fate specification and follicle stem cell maintenance in Drosophila oogenesis.

TitleCastor is required for Hedgehog-dependent cell-fate specification and follicle stem cell maintenance in Drosophila oogenesis.
Publication TypeJournal Article
Year of Publication2013
AuthorsChang Y-C, Jang AC-C, Lin C-H, Montell DJ
JournalProc Natl Acad Sci U S A
Volume110
Issue19
PaginationE1734-42
Date Published2013 May 07
ISSN1091-6490
KeywordsAnimals, Cell Lineage, DNA-Binding Proteins, Drosophila melanogaster, Drosophila Proteins, Epistasis, Genetic, Eye Proteins, Female, Gene Expression Regulation, Developmental, Gene Knockdown Techniques, Genetic Complementation Test, Hedgehog Proteins, Immunohistochemistry, Oogenesis, Ovarian Follicle, Stem Cells
Abstract

<p>Asymmetric division of stem cells results in both self-renewal and differentiation of daughters. Understanding the molecules and mechanisms that govern differentiation of specific cell types from adult tissue stem cells is a major challenge in developmental biology and regenerative medicine. Drosophila follicle stem cells (FSCs) represent an excellent model system to study adult stem cell behavior; however, the earliest stages of follicle cell differentiation remain largely mysterious. Here we identify Castor (Cas) as a nuclear protein that is expressed in FSCs and early follicle cell precursors and then is restricted to differentiated polar and stalk cells once egg chambers form. Cas is required for FSC maintenance and polar and stalk cell fate specification. Eyes absent (Eya) is excluded from polar and stalk cells and represses their fate by inhibiting Cas expression. Hedgehog signaling is essential to repress Eya to allow Cas expression in polar and stalk cells. Finally, we show that the complementary patterns of Cas and Eya reveal the gradual differentiation of polar and stalk precursor cells at the earliest stages of their development. Our studies provide a marker for cell fates in this model and insight into the molecular and cellular mechanisms by which FSC progeny diverge into distinct fates.</p>

DOI10.1073/pnas.1300725110
Alternate JournalProc. Natl. Acad. Sci. U.S.A.
PubMed ID23610413
PubMed Central IDPMC3651482
Grant ListR01 GM046425 / GM / NIGMS NIH HHS / United States
GM46425 / GM / NIGMS NIH HHS / United States