Smaug, a novel and conserved protein, contributes to repression of nanos mRNA translation in vitro

被引:117
作者
Smibert, CA
Lie, YS
Shillinglaw, W
Henzel, WJ
Macdonald, PM
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[2] Genentech Inc, Dept Prot Chem, S San Francisco, CA 94080 USA
关键词
Drosophila; embryo; RNA-binding protein;
D O I
10.1017/S1355838299991392
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
Proper deployment of Nanos protein at the posterior of the Drosophila embryo, where it directs posterior development, requires a combination of RNA localization and translational controls. These controls ensure that only the posteriorly-localized nanos mRNA is translated, whereas unlocalized nanos mRNA is translationally repressed. Here we describe cloning of the gene encoding Smaug, an RNA-binding protein that interacts with the sequences, SREs, in the nanos mRNA that mediate translational repression. Using an in vitro translation assay, we demonstrate that SRE-dependent repression occurs in extracts from early stage embryos, Immunodepletion of Smaug from the extracts eliminates repression, consistent with the notion that Smaug is involved. Smaug is a novel gene and the existence of potential mammalian Smaug homologs raises the possibility that Smaug represents a new class of conserved translational repressor.
引用
收藏
页码:1535 / 1547
页数:13
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