Rongo C, Gavis E R, Lehmann R
Whitehead Institute for Biomedical Research, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02142, USA.
Development. 1995 Sep;121(9):2737-46. doi: 10.1242/dev.121.9.2737.
The site of oskar RNA and protein localization within the oocyte determines where in the embryo primordial germ cells form and where the abdomen develops. Initiation of oskar RNA localization requires the activity of several genes. We show that ovaries mutant for any of these genes lack Oskar protein. Using various transgenic constructs we have determined that sequences required for oskar RNA localization and translational repression map to the oskar 3'UTR, while sequences involved in the correct temporal activation of translation reside outside the oskar 3'UTR. Upon localization of oskar RNA and protein at the posterior pole, Oskar protein is required to maintain localization of oskar RNA throughout oogenesis. Stable anchoring of a transgenic reporter RNA at the posterior pole is disrupted by oskar nonsense mutations. We propose that initially localization of oskar RNA permits translation into Oskar protein and that subsequently Oskar protein regulates its own RNA localization through a positive feedback mechanism.
卵母细胞内oskar RNA和蛋白质的定位位点决定了胚胎中原始生殖细胞形成的位置以及腹部发育的位置。oskar RNA定位的起始需要几个基因的活性。我们发现,这些基因中任何一个发生突变的卵巢都缺乏Oskar蛋白。通过各种转基因构建体,我们确定oskar RNA定位和翻译抑制所需的序列定位于oskar 3'UTR,而参与翻译正确时间激活的序列位于oskar 3'UTR之外。当oskar RNA和蛋白质在后极定位后,在整个卵子发生过程中需要Oskar蛋白来维持oskar RNA的定位。oskar无义突变会破坏转基因报告RNA在后极的稳定锚定。我们提出,最初oskar RNA的定位允许其翻译成Oskar蛋白,随后Oskar蛋白通过正反馈机制调节其自身RNA的定位。