Literature DB >> 18050484

Cell division.

Karen Oegema1, Anthony A Hyman.   

Abstract

The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.

Entities:  

Mesh:

Year:  2006        PMID: 18050484      PMCID: PMC4780891          DOI: 10.1895/wormbook.1.72.1

Source DB:  PubMed          Journal:  WormBook        ISSN: 1551-8507


  62 in total

Review 1.  EGG molecules couple the oocyte-to-embryo transition with cell cycle progression.

Authors:  Jean M Parry; Andrew Singson
Journal:  Results Probl Cell Differ       Date:  2011

2.  A novel function of Rab5 in mitosis.

Authors:  Letizia Lanzetti
Journal:  Small GTPases       Date:  2012-06-14

3.  Caenorhabditis elegans EFA-6 limits microtubule growth at the cell cortex.

Authors:  Sean M O'Rourke; Sara N Christensen; Bruce Bowerman
Journal:  Nat Cell Biol       Date:  2010-11-14       Impact factor: 28.824

4.  Molecular analysis of mitotic chromosome condensation using a quantitative time-resolved fluorescence microscopy assay.

Authors:  Paul S Maddox; Nathan Portier; Arshad Desai; Karen Oegema
Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-27       Impact factor: 11.205

5.  Systematic analysis in Caenorhabditis elegans reveals that the spindle checkpoint is composed of two largely independent branches.

Authors:  Anthony Essex; Alexander Dammermann; Lindsay Lewellyn; Karen Oegema; Arshad Desai
Journal:  Mol Biol Cell       Date:  2008-12-24       Impact factor: 4.138

6.  Regulation of cortical contractility and spindle positioning by the protein phosphatase 6 PPH-6 in one-cell stage C. elegans embryos.

Authors:  Katayoun Afshar; Michael E Werner; Yu Chung Tse; Michael Glotzer; Pierre Gönczy
Journal:  Development       Date:  2010-01       Impact factor: 6.868

7.  The cytokinesis formins from the nematode worm and fission yeast differentially mediate actin filament assembly.

Authors:  Erin M Neidt; Colleen T Skau; David R Kovar
Journal:  J Biol Chem       Date:  2008-06-23       Impact factor: 5.157

8.  A model of cytoplasmically driven microtubule-based motion in the single-celled Caenorhabditis elegans embryo.

Authors:  Tamar Shinar; Miyeko Mana; Fabio Piano; Michael J Shelley
Journal:  Proc Natl Acad Sci U S A       Date:  2011-06-13       Impact factor: 11.205

9.  Zinc availability during germline development impacts embryo viability in Caenorhabditis elegans.

Authors:  Adelita D Mendoza; Teresa K Woodruff; Sarah M Wignall; Thomas V O'Halloran
Journal:  Comp Biochem Physiol C Toxicol Pharmacol       Date:  2016-09-21       Impact factor: 3.228

10.  A Nucleoporin Docks Protein Phosphatase 1 to Direct Meiotic Chromosome Segregation and Nuclear Assembly.

Authors:  Neil Hattersley; Dhanya Cheerambathur; Mark Moyle; Marine Stefanutti; Amelia Richardson; Kian-Yong Lee; Julien Dumont; Karen Oegema; Arshad Desai
Journal:  Dev Cell       Date:  2016-09-12       Impact factor: 12.270

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