drosophila ge-1 promotes p body formation and oskar mrna localization果蝇p ge-1促进身体形成和奥斯卡·mrna本地化.pdfVIP

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drosophila ge-1 promotes p body formation and oskar mrna localization果蝇p ge-1促进身体形成和奥斯卡·mrna本地化.pdf

drosophila ge-1 promotes p body formation and oskar mrna localization果蝇p ge-1促进身体形成和奥斯卡·mrna本地化

Drosophila Ge-1 Promotes P Body Formation and oskar mRNA Localization Shih-Jung Fan, Virginie Marchand, Anne Ephrussi* Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany Abstract mRNA localization coupled with translational control is a widespread and conserved strategy that allows the localized production of proteins within eukaryotic cells. In Drosophila, oskar (osk) mRNA localization and translation at the posterior pole of the oocyte are essential for proper patterning of the embryo. Several P body components are involved in osk mRNA localization and translational repression, suggesting a link between P bodies and osk RNPs. In cultured mammalian cells, Ge- 1 protein is required for P body formation. Combining genetic, biochemical and immunohistochemical approaches, we show that, in vivo, Drosophila Ge-1 (dGe-1) is an essential gene encoding a P body component that promotes formation of these structures in the germline. dGe-1 partially colocalizes with osk mRNA and is required for osk RNP integrity. Our analysis reveals that although under normal conditions dGe-1 function is not essential for osk mRNA localization, it becomes critical when other components of the localization machinery, such as staufen, Drosophila decapping protein 1 and barentsz are limiting. Our findings suggest an important role of dGe-1 in optimization of the osk mRNA localization process required for patterning the Drosophila embryo. Citation: Fan S-J, Marchand V, Ephrussi A (2011) Drosophila Ge-1 Promotes P Body Formation and oskar mRNA Localization. PLoS ONE 6(5): e20612. doi:10.1371/ journal.pone.0020612 Editor: Jessica Esther Treisman, Skirball Institute of Biomolecular Medicine - New York University Medical Center, United States of America Received February 8, 2011; Accepted May 5, 2011; Published May 31, 2011 Copyright:

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