The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway

被引:77
作者
Costa, A
Wang, Y
Dockendorff, TC
Erdjument-Bromage, H
Tempst, P
Schedl, P [1 ]
Jongens, TA
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[2] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[3] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
[4] Miami Univ, Dept Zool, Oxford, OH 45056 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.devcel.2005.01.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Translational regulation of maternal mRNAs in distinct temporal and spatial patterns underlies many key decisions in developing eggs and embryos. In Drosophila, Orb is responsible for mediating the translational activation of mRNAs localized within the developing oocyte. Orb is a germline-specific RNA binding protein and is one of the founding members of the CPEB family of translational regulators. Here we show that Orb associates with the Drosophila Fragile X Mental Retardation (dFMR1) protein as part of a ribonucleoprotein complex that controls the localized translation of mRNAs in developing egg chambers. One of the key orb regulatory targets is orb mRNA, and this autoregulatory activity is critical for ensuring that Orb protein is expressed at high levels in the oocyte. We show that dFMR1 functions as a negative regulator in the orb autoregulatory circuit, downregulating orb mRNA translation.
引用
收藏
页码:331 / 342
页数:12
相关论文
共 43 条
[11]   Examination of micro-tip reversed-phase liquid chromatographic extraction of peptide pools for mass spectrometric analysis [J].
Erdjument-Bromage, H ;
Lui, M ;
Lacomis, L ;
Grewal, A ;
Annan, RS ;
McNulty, DE ;
Carr, SA ;
Tempst, P .
JOURNAL OF CHROMATOGRAPHY A, 1998, 826 (02) :167-181
[12]   Tuning of an electrospray ionization source for maximum peptide-ion transmission into a mass spectrometer [J].
Geromanos, S ;
Freckleton, G ;
Tempst, P .
ANALYTICAL CHEMISTRY, 2000, 72 (04) :777-790
[13]   Activation/division of lymphocytes results in increased levels of cytoplasmic activation/proliferation-associated protein-1: Prototype of a new family of proteins [J].
Grill, B ;
Wilson, GM ;
Zhang, KX ;
Wang, B ;
Doyonnas, R ;
Quadroni, F ;
Schrader, JW .
JOURNAL OF IMMUNOLOGY, 2004, 172 (04) :2389-2400
[14]   CPEB IS A SPECIFICITY FACTOR THAT MEDIATES CYTOPLASMIC POLYADENYLATION DURING XENOPUS OOCYTE MATURATION [J].
HAKE, LE ;
RICHTER, JD .
CELL, 1994, 79 (04) :617-627
[15]   N-methyl-D-aspartate receptor signaling results in Aurora kinase-catalyzed CPEB phosphorylation and αCaMKII mRNA polyadenylation at synapses [J].
Huang, YS ;
Jung, MY ;
Sarkissian, M ;
Richter, JD .
EMBO JOURNAL, 2002, 21 (09) :2139-2148
[16]   Facilitation of dendritic mRNA transport by CPEB [J].
Huang, YS ;
Carson, JH ;
Barbarese, E ;
Richter, JD .
GENES & DEVELOPMENT, 2003, 17 (05) :638-653
[17]  
Huynh JR, 2000, DEVELOPMENT, V127, P2785
[18]   A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins [J].
Ishizuka, A ;
Siomi, MC ;
Siomi, H .
GENES & DEVELOPMENT, 2002, 16 (19) :2497-2508
[19]  
Jin SW, 2001, GENETICS, V159, P1617
[20]   Translational regulation and RNA localization in Drosophila oocytes and embryos [J].
Johnstone, O ;
Lasko, P .
ANNUAL REVIEW OF GENETICS, 2001, 35 :365-406