Kaneshiro Kazuki, Miyauchi Maki, Tanigawa Yoko, Ikenishi Kohji, Komiya Tohru
Department of Biological Function, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi, Osaka 558-8585, Japan.
Biochem Biophys Res Commun. 2007 Apr 20;355(4):902-6. doi: 10.1016/j.bbrc.2007.02.059. Epub 2007 Feb 20.
Using a large-scale in situ hybridization screening, we found that the mRNA coding for Xenopus glutamate receptor interacting protein 2 (XGRIP2) was localized to the germ plasm of Xenopus laevis. The mRNA is maternally transcribed in oocytes and, during maturation, transported to the vegetal germ plasm through the late pathway where VegT and Vg1 mRNAs are transported. In the 3'-untranslated region (UTR) of the mRNA, there are clusters of E2 and VM1 localization motifs that were reported to exist in the mRNAs classified as the late pathway group. With in situ hybridization to the sections of embryos, the signal could be detected in the cytoplasm of migrating presumptive primordial germ cells (pPGCs) until stage 35. At stage 40, when the cells cease to migrate and reach the dorsal mesentery, the signal disappeared. A possible role of XGRIP2 in pPGCs of Xenopus will be discussed.
通过大规模原位杂交筛选,我们发现非洲爪蟾谷氨酸受体相互作用蛋白2(XGRIP2)的编码mRNA定位于非洲爪蟾的生殖质中。该mRNA在卵母细胞中由母体转录,并在成熟过程中通过晚期途径运输到植物性生殖质,VegT和Vg1 mRNA也是通过该途径运输的。在该mRNA的3'非翻译区(UTR)中,存在E2和VM1定位基序簇,据报道这些基序存在于归类为晚期途径组的mRNA中。通过对胚胎切片进行原位杂交,直到第35阶段都能在迁移的假定原始生殖细胞(pPGC)的细胞质中检测到信号。在第40阶段,当细胞停止迁移并到达背系膜时,信号消失。本文将讨论XGRIP2在非洲爪蟾pPGC中的可能作用。