The transcriptional factor CF2 is a mediator of EGF-R-activated dorsoventral patterning in Drosophila oogenesis.
Details
Serval ID
serval:BIB_0EDBF783168E
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
The transcriptional factor CF2 is a mediator of EGF-R-activated dorsoventral patterning in Drosophila oogenesis.
Journal
Genes & development
ISSN
0890-9369 (Print)
ISSN-L
0890-9369
Publication state
Published
Issued date
01/06/1996
Volume
10
Number
11
Pages
1411-1421
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S.
Publication Status: ppublish
Publication Status: ppublish
Abstract
Establishment of dorsoventral polarity during Drosophila oogenesis requires localized intercellular communication between the follicular cells and the oocyte. This is initiated by the transmission of a "dorsal signal" from the oocyte to the anterior dorsal follicle cells by the EGF receptor (EGF-R) pathway and is followed by transmission of a second signal from the ventral follicle cells back to the embryo. We show that the zinc finger transcription factor CF2 participates in these processes. CF2 is suppressed by EGF-R signaling in the anterior dorsal follicle cells. Altered expression patterns of CF2 result in specific dorsoventral patterning defects in egg chambers and in embryos, as demonstrated phenotypically and with molecular markers. CF2 appears to act as a repressor of dorsal follicle cell fates and specifically as a repressor of the rhomboid gene transcription.
Keywords
Animals, Animals, Genetically Modified, DNA-Binding Proteins/physiology, Drosophila/embryology, Drosophila Proteins, Female, Gene Expression Regulation, Developmental, Genomic Imprinting, Male, Mosaicism, Mothers, Oogenesis/physiology, Phenotype, Receptor, Epidermal Growth Factor/physiology, Signal Transduction, Transcription Factors/physiology
Pubmed
Create date
06/03/2017 17:23
Last modification date
20/08/2019 12:35