Literature DB >> 16678775

Drosophila decapping protein 1, dDcp1, is a component of the oskar mRNP complex and directs its posterior localization in the oocyte.

Ming-Der Lin1, Shih-Jung Fan, Wei-Shan Hsu, Tze-Bin Chou.   

Abstract

In Drosophila, posterior deposition of oskar (osk) mRNA in oocytes is critical for both pole cell and abdomen formation. Exon junction complex components, translational regulation factors, and other proteins form an RNP complex that is essential for directing osk mRNA to the posterior of the oocyte. Until now, it has not been clear whether the mRNA degradation machinery is involved in regulating osk mRNA deposition. Here we show that Drosophila decapping protein 1, dDcp1, is a posterior group gene required for the transport of osk mRNA. In oocytes, dDcp1 is localized posteriorly in an osk mRNA position- and dosage-dependent manner. In nurse cells, dDcp1 colocalizes with dDcp2 and Me31B in discrete foci that may be related to processing bodies (P bodies), which are sites of active mRNA degradation. Thus, as well as being a general factor required for mRNA decay, dDcp1 is an essential component of the osk mRNP localization complex.

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Year:  2006        PMID: 16678775     DOI: 10.1016/j.devcel.2006.02.021

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  35 in total

Review 1.  New insights into the regulation of RNP granule assembly in oocytes.

Authors:  Jennifer A Schisa
Journal:  Int Rev Cell Mol Biol       Date:  2012       Impact factor: 6.813

2.  U bodies are cytoplasmic structures that contain uridine-rich small nuclear ribonucleoproteins and associate with P bodies.

Authors:  Ji-Long Liu; Joseph G Gall
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-26       Impact factor: 11.205

3.  A genome-wide RNAi screen reveals that mRNA decapping restricts bunyaviral replication by limiting the pools of Dcp2-accessible targets for cap-snatching.

Authors:  Kaycie C Hopkins; Laura M McLane; Tariq Maqbool; Debasis Panda; Beth Gordesky-Gold; Sara Cherry
Journal:  Genes Dev       Date:  2013-07-01       Impact factor: 11.361

4.  Similar modes of interaction enable Trailer Hitch and EDC3 to associate with DCP1 and Me31B in distinct protein complexes.

Authors:  Felix Tritschler; Ana Eulalio; Sigrun Helms; Steffen Schmidt; Murray Coles; Oliver Weichenrieder; Elisa Izaurralde; Vincent Truffault
Journal:  Mol Cell Biol       Date:  2008-09-02       Impact factor: 4.272

Review 5.  RNA granules in germ cells.

Authors:  Ekaterina Voronina; Geraldine Seydoux; Paolo Sassone-Corsi; Ippei Nagamori
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-12-01       Impact factor: 10.005

6.  A genetic in vivo system to detect asymmetrically distributed RNA.

Authors:  N JayaNandanan; Elizabeth R Gavis; Veit Riechmann; Maria Leptin
Journal:  EMBO Rep       Date:  2011-10-28       Impact factor: 8.807

Review 7.  Effects of stress and aging on ribonucleoprotein assembly and function in the germ line.

Authors:  Jennifer A Schisa
Journal:  Wiley Interdiscip Rev RNA       Date:  2013-11-13       Impact factor: 9.957

8.  Identification of Drosophila and human 7-methyl GMP-specific nucleotidases.

Authors:  Juliane Buschmann; Bodo Moritz; Mandy Jeske; Hauke Lilie; Angelika Schierhorn; Elmar Wahle
Journal:  J Biol Chem       Date:  2012-12-05       Impact factor: 5.157

9.  P-body components are required for Ty1 retrotransposition during assembly of retrotransposition-competent virus-like particles.

Authors:  Mary Ann Checkley; Kunio Nagashima; Stephen J Lockett; Katherine M Nyswaner; David J Garfinkel
Journal:  Mol Cell Biol       Date:  2009-11-09       Impact factor: 4.272

10.  Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control.

Authors:  Alessandra di Penta; Valentina Mercaldo; Fulvio Florenzano; Sebastian Munck; M Teresa Ciotti; Francesca Zalfa; Delio Mercanti; Marco Molinari; Claudia Bagni; Tilmann Achsel
Journal:  J Cell Biol       Date:  2009-02-02       Impact factor: 10.539

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