Translational repression by the oocyte-specific protein P100 in Xenopus

Clicks: 217
ID: 271548
2010
Article Quality & Performance Metrics
Overall Quality Improving Quality
0.0 /100
Combines engagement data with AI-assessed academic quality
AI Quality Assessment
Not analyzed
The translational regulation of maternal mRNAs is one of the most important steps in the control of temporal–spatial gene expression during oocyte maturation and early embryogenesis in various species. Recently, it has become clear that protein components of mRNPs play essential roles in the translational regulation of maternal mRNAs. In the present study, we investigated the function of P100 in Xenopus oocytes. P100 exhibits sequence conservation with budding yeast Pat1 and is likely the orthologue of human Pat1a (also called PatL2). P100 is maternally expressed in immature oocytes, but disappears during oocyte maturation. In oocytes, P100 is an RNA binding component of ribosome-free mRNPs, associating with other mRNP components such as Xp54, xRAP55 and CPEB. Translational repression by overexpression of P100 occurred when reporter mRNAs were injected into oocytes. Intriguingly, we found that when P100 was overexpressed in the oocytes, the kinetics of oocyte maturation was considerably retarded. In addition, overexpression of P100 in oocytes significantly affected the accumulation of c-Mos and cyclin B1 during oocyte maturation. These results suggest that P100 plays a role in regulating the translation of specific maternal mRNAs required for the progression of Xenopus oocyte maturation
Reference Key
matsumoto2010developmentaltranslational Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Yoriko Nakamura,Kimio J. Tanaka,Maki Miyauchi,Lin Huang,Masafumi Tsujimoto,Ken Matsumoto;Yoriko Nakamura;Kimio J. Tanaka;Maki Miyauchi;Lin Huang;Masafumi Tsujimoto;Ken Matsumoto;
Journal Developmental biology
Year 2010
DOI 10.1016/j.ydbio.2010.05.006
URL
Keywords

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.