Translational repression of the Drosophila nanos mRNA involves the RNA helicase Belle and RNA coating by Me31B and Trailer hitch

被引:46
|
作者
Goetze, Michael [1 ]
Dufourt, Jeremy [2 ]
Ihling, Christian [3 ]
Rammelt, Christiane [1 ]
Pierson, Stephanie [2 ]
Sambrani, Nagraj [2 ]
Temme, Claudia [1 ,4 ]
Sinz, Andrea [3 ]
Simonelig, Martine [2 ]
Wahle, Elmar [1 ]
机构
[1] Martin Luther Univ Halle Wittenberg, Inst Biochem & Biotechnol, D-06099 Halle, Germany
[2] Univ Montpellier, CNRS, UMR9002, Inst Human Genet, F-34396 Montpellier 5, France
[3] Martin Luther Univ Halle Wittenberg, Inst Pharm, D-06099 Halle, Germany
[4] IDT, Pharmapk, D-06861 Dessau Rosslau, Germany
关键词
translational repression; maternal RNA; deadenylation; TO-ZYGOTIC TRANSITION; BINDING-PROTEIN; CCR4-NOT COMPLEX; IN-VIVO; EIF4E-BINDING PROTEIN; DECAPPING ACTIVATORS; OSKAR TRANSLATION; XENOPUS OOCYTES; CELL-FORMATION; SMAUG;
D O I
10.1261/rna.062208.117
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
Translational repression of maternal mRNAs is an essential regulatory mechanism during early embryonic development. Repression of the Drosophila nanos mRNA, required for the formation of the anterior-posterior body axis, depends on the protein Smaug binding to two Smaug recognition elements (SREs) in the nanos 3' UTR. In a comprehensive mass spectrometric analysis of the SRE-dependent repressor complex, we identified Smaug, Cup, Me31B, Trailer hitch, eIF4E, and PABPC, in agreement with earlier data. As a novel component, the RNA-dependent ATPase Belle (DDX3) was found, and its involvement in deadenylation and repression of nanos was confirmed in vivo. Smaug, Cup, and Belle bound stoichiometrically to the SREs, independently of RNA length. Binding of Me31B and Tral was also SRE-dependent, but their amounts were proportional to the length of the RNA and equimolar to each other. We suggest that "coating" of the RNA by a Me31B.Tral complex may be at the core of repression.
引用
收藏
页码:1552 / 1568
页数:17
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