Literature DB >> 14752008

Roles of Bifocal, Homer, and F-actin in anchoring Oskar to the posterior cortex of Drosophila oocytes.

Kavita Babu1, Yu Cai, Sami Bahri, Xiaohang Yang, William Chia.   

Abstract

Transport, translation, and anchoring of osk mRNA and proteins are essential for posterior patterning of Drosophila embryos. Here we show that Homer and Bifocal act redundantly to promote posterior anchoring of the osk gene products. Disruption of actin microfilaments, which causes delocalization of Bifocal but not Homer from the oocyte cortex, severely disrupts anchoring of osk gene products only when Homer (not Bifocal) is absent. Our data suggest that two processes, one requiring Bifocal and an intact F-actin cytoskeleton and a second requiring Homer but independent of intact F-actin, may act redundantly to mediate posterior anchoring of the osk gene products.

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Year:  2004        PMID: 14752008      PMCID: PMC324420          DOI: 10.1101/gad.282604

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  35 in total

1.  A Drosophila melanogaster homologue of Caenorhabditis elegans par-1 acts at an early step in embryonic-axis formation.

Authors:  P Tomancak; F Piano; V Riechmann; K C Gunsalus; K J Kemphues; A Ephrussi
Journal:  Nat Cell Biol       Date:  2000-07       Impact factor: 28.824

Review 2.  Microtubules, motors, and mRNA localization mechanisms: watching fluorescent messages move.

Authors:  W M Saxton
Journal:  Cell       Date:  2001-12-14       Impact factor: 41.582

3.  Bifocal is a downstream target of the Ste20-like serine/threonine kinase misshapen in regulating photoreceptor growth cone targeting in Drosophila.

Authors:  Wenjing Ruan; Hong Long; Dac Hien Vuong; Yong Rao
Journal:  Neuron       Date:  2002-12-05       Impact factor: 17.173

4.  Interaction with protein phosphatase 1 Is essential for bifocal function during the morphogenesis of the Drosophila compound eye.

Authors:  N R Helps; P T Cohen; S M Bahri; W Chia; K Babu
Journal:  Mol Cell Biol       Date:  2001-03       Impact factor: 4.272

5.  Cupidin, an isoform of Homer/Vesl, interacts with the actin cytoskeleton and activated rho family small GTPases and is expressed in developing mouse cerebellar granule cells.

Authors:  Y Shiraishi; A Mizutani; H Bito; K Fujisawa; S Narumiya; K Mikoshiba; T Furuichi
Journal:  J Neurosci       Date:  1999-10-01       Impact factor: 6.167

6.  Mutation of Drosophila homer disrupts control of locomotor activity and behavioral plasticity.

Authors:  Thierry T Diagana; Ulrich Thomas; Sergei N Prokopenko; Bo Xiao; Paul F Worley; John B Thomas
Journal:  J Neurosci       Date:  2002-01-15       Impact factor: 6.167

7.  Kinesin I-dependent cortical exclusion restricts pole plasm to the oocyte posterior.

Authors:  Byeong-Jik Cha; Laura R Serbus; Birgit S Koppetsch; William E Theurkauf
Journal:  Nat Cell Biol       Date:  2002-08       Impact factor: 28.824

8.  Dmoesin controls actin-based cell shape and polarity during Drosophila melanogaster oogenesis.

Authors:  Cédric Polesello; Isabelle Delon; Philippe Valenti; Pierre Ferrer; François Payre
Journal:  Nat Cell Biol       Date:  2002-10       Impact factor: 28.824

9.  Lava lamp, a novel peripheral golgi protein, is required for Drosophila melanogaster cellularization.

Authors:  J C Sisson; C Field; R Ventura; A Royou; W Sullivan
Journal:  J Cell Biol       Date:  2000-11-13       Impact factor: 10.539

10.  Oskar anchoring restricts pole plasm formation to the posterior of the Drosophila oocyte.

Authors:  Nathalie F Vanzo; Anne Ephrussi
Journal:  Development       Date:  2002-08       Impact factor: 6.868

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  20 in total

1.  A late phase of germ plasm accumulation during Drosophila oogenesis requires lost and rumpelstiltskin.

Authors:  Kristina S Sinsimer; Roshan A Jain; Seema Chatterjee; Elizabeth R Gavis
Journal:  Development       Date:  2011-07-13       Impact factor: 6.868

2.  Receptor tyrosine phosphatases regulate birth order-dependent axonal fasciculation and midline repulsion during development of the Drosophila mushroom body.

Authors:  Mitsuhiko Kurusu; Kai Zinn
Journal:  Mol Cell Neurosci       Date:  2008-02-13       Impact factor: 4.314

3.  Patterns of molecular evolution of the germ line specification gene oskar suggest that a novel domain may contribute to functional divergence in Drosophila.

Authors:  Abha Ahuja; Cassandra G Extavour
Journal:  Dev Genes Evol       Date:  2014-01-10       Impact factor: 0.900

Review 4.  mRNA localization and translational control in Drosophila oogenesis.

Authors:  Paul Lasko
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-10-01       Impact factor: 10.005

Review 5.  Subcellular Specialization and Organelle Behavior in Germ Cells.

Authors:  Yukiko M Yamashita
Journal:  Genetics       Date:  2018-01       Impact factor: 4.562

6.  Oskar-induced endocytic activation and actin remodeling for anchorage of the Drosophila germ plasm.

Authors:  Tsubasa Tanaka; Akira Nakamura
Journal:  Bioarchitecture       Date:  2011-05

7.  The Drosophila RNA-binding protein Lark is required for localization of Dmoesin to the oocyte cortex during oogenesis.

Authors:  Gerard P McNeil; Manpreet Kaur; Sheryl Purrier; Ruth Kang
Journal:  Dev Genes Evol       Date:  2008-10-29       Impact factor: 0.900

8.  Genome-wide screen reveals APC-associated RNAs enriched in cell protrusions.

Authors:  Stavroula Mili; Konstadinos Moissoglu; Ian G Macara
Journal:  Nature       Date:  2008-05-01       Impact factor: 49.962

9.  Germ plasm anchoring is a dynamic state that requires persistent trafficking.

Authors:  Kristina S Sinsimer; Jack J Lee; Stephan Y Thiberge; Elizabeth R Gavis
Journal:  Cell Rep       Date:  2013-11-27       Impact factor: 9.423

Review 10.  Germ Plasm Biogenesis--An Oskar-Centric Perspective.

Authors:  Ruth Lehmann
Journal:  Curr Top Dev Biol       Date:  2016-02-13       Impact factor: 4.897

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