國立臺灣大學分子與細胞生物學研究所周子賓2006-07-252018-07-062006-07-252018-07-062005http://ntur.lib.ntu.edu.tw//handle/246246/5051In Drosophila, the posterior deposition of oskar (osk) mRNA in the oocyte is critical for pole cell and abdomen formation. Exon junction complex components, translational regulation factors and other proteins form the RNP complex essential for directing osk mRNA to the posterior end of the oocyte. Until now, it has not been clear whether the mRNA degradation machinery is involved in regulating osk mRNA deposition. Here we show that Drosophila decapping protein 1, dDcp1, a general factor required for mRNA degradation, is also a novel component of the osk mRNP complex essential for osk mRNA posterior deposition. During oogenesis, dDcp1 can interact with Exuperantia (Exu) in an RNA-dependent manner while osk mRNA is not yet set for degradation and is required for the proper localization of Exu, Ypsilon Schachtel (Yps) and Oo18 RNA binding (Orb). Clearly, dDcp1 is required for an elaborate coupling of osk mRNA localization in the oocyte and its degradation in the embryo.application/pdf214440 bytesapplication/pdfzh-TW國立臺灣大學分子與細胞生物學研究所reporthttp://ntur.lib.ntu.edu.tw/bitstream/246246/5051/1/932311B002027.pdf