Abstract
In Drosophila oogenesis, follicle cells derived from somatic tissue surround the oocyte and play key roles in generating properly polarized oocytes. During the later steps of oogenesis, follicle cells are involved in secretion of proteins that make the eggshell, an essential protective layer for the oocyte. Although studies on the signaling processes to make polarized oocytes have been progressed very far, studies on the mechanisms for eggshell formation is not clear yet. To elucidate the underlying mechanism in eggshell formation, we used a differential display screen to isolate genes that are specifically expressed during the later stages of oogenesis, and isolated a novel gene, Femcoat. Femcoat encodes a putative chorion membrane protein that contains many highly charged residues and has a putative signal peptide. Femcoat is expressed specifically in the follicle cells with a punctate staining pattern typical of secreted proteins, and becomes cross-linked heavily at the final steps of oogenesis. To identify the developmental role of Femcoat in eggshell formation, we performed an inducible double stranded RNA mediated interference (dsRNAi) method to specifically reduce Femcoat expression during oogenesis in adult flies. Electron microscopy analysis of egg chambers from these flies showed defects in chorion formation. These pieces of evidence demonstrated that Femcoat is necessary for eggshell formation, especially during chorion synthesis. Our results demonstrate that inducible dsRNAi analysis can be effective in determining the developmental function of novel genes.
Original language | English |
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Pages (from-to) | 61-70 |
Number of pages | 10 |
Journal | Mechanisms of Development |
Volume | 110 |
Issue number | 1-2 |
DOIs | |
Publication status | Published - 2002 Jan |
Bibliographical note
Funding Information:We thank G. Waring for generously providing antibodies against several chorion and vitelline membrane proteins, and C. Hashimoto and the Bloomington and the Umea fly stock center for nudel and other fly stocks. We thank Mijung Kang at National Center for Inter-University Research for her excellent assistance in electron microscopy. This work was supported by a grant from Ministry of Science and Technology of Korea (f-4-09 of 21C frontier functional genome project) to J.K.-H.
All Science Journal Classification (ASJC) codes
- Embryology
- Developmental Biology