Two Piwi proteins, Xiwi and Xili, are expressed in the Xenopus female germline

被引:49
作者
Wilczynska, Anna [1 ]
Minshall, Nicola [1 ]
Armisen, Javier [1 ,2 ]
Miska, Eric A. [1 ,2 ]
Standart, Nancy [1 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
[2] Univ Cambridge, Wellcome Trust Canc Res UK Gurdon Inst, Cambridge CB2 1QN, England
基金
英国生物技术与生命科学研究理事会;
关键词
Argonaute; piRNA; gene silencing; oocyte; NOVO DNA METHYLATION; SMALL RNAS; DROSOPHILA-MELANOGASTER; CELL-DIFFERENTIATION; ARGONAUTE PROTEINS; FAMILY-MEMBERS; PIRNA COMPLEX; MOUSE OOCYTES; STEM-CELLS; GENE;
D O I
10.1261/rna.1422509
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Argonaute superfamily is a large family of RNA-binding proteins involved in gene regulation mediated by small noncoding RNA and characterized by the presence of PAZ and PIWI domains. The family consists of two branches, the Ago and the Piwi clade. Piwi proteins bind to 21-30-nucleotide-long Piwi-interacting RNAs (piRNAs), which map primarily to transposons and repeated sequence elements. Piwi/piRNAs are important regulators of gametogenesis and have been proposed to play roles in transposon silencing, DNA methylation, transcriptional silencing, and/or post-transcriptional control of translation and RNA stability. Most reports to date have concentrated on the Piwi family members in the male germline. We have identified four Piwi proteins in Xenopus and demonstrate that two, namely, Xiwi1b and Xili, are expressed in the oocyte and early embryo. Xiwi1 and Xili are predominantly found in small, separate complexes, and we do not detect significant interaction of Piwi proteins with the cap-binding complex. Putative nuclear localization and export signals were identified in Xiwi1 and Xili, supporting our observation that Xiwi1, but not Xili, is a nucleo-cytoplasmic protein. Furthermore, by immunoprecipitation of small RNAs, we establish Xiwi1 as a bona fide Piwi protein. These results suggest that the Piwi/piRNA pathway is active in translationally repressed oocytes. This is a significant finding as the Xenopus model provides an excellent tool to study post-transcriptional mechanisms.
引用
收藏
页码:337 / 345
页数:9
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