Literature DB >> 34972943

Methods for Investigating Cell Division Mechanisms in C. elegans.

Ian D Wolff1, Nikita S Divekar1, Sarah M Wignall2.   

Abstract

The nematode Caenorhabditis elegans is a widely used model organism for the study of mitotic and meiotic cell division. These self-fertilizing worms are particularly advantageous for such studies because they rapidly reproduce (each worm lays ~250 eggs in only 3-4 days) and the cell division machinery is highly conserved between worms and humans. Worms are also genetically tractable and proteins can be readily depleted using RNA interference (RNAi), allowing for the characterization of protein function in vivo. To assess phenotypes, spindles can be directly visualized within the worm using fluorescent protein tags or embryos can be dissected out of the worm and immunostained. A combination of these techniques allows comprehensive characterization of a protein's function in a relatively short time span. Here, we describe methods for each of these techniques: RNA interference through feeding, in utero live imaging, in utero fixed imaging, and immunofluorescence.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  GFP; Meiosis; Microscopy; Oocyte; RNAi

Mesh:

Substances:

Year:  2022        PMID: 34972943      PMCID: PMC8901195          DOI: 10.1007/978-1-0716-1904-9_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  34 in total

1.  Functional genomic analysis of C. elegans chromosome I by systematic RNA interference.

Authors:  A G Fraser; R S Kamath; P Zipperlen; M Martinez-Campos; M Sohrmann; J Ahringer
Journal:  Nature       Date:  2000-11-16       Impact factor: 49.962

2.  KLP-18, a Klp2 kinesin, is required for assembly of acentrosomal meiotic spindles in Caenorhabditis elegans.

Authors:  Christoph Segbert; Rosemarie Barkus; Jim Powers; Susan Strome; William M Saxton; Olaf Bossinger
Journal:  Mol Biol Cell       Date:  2003-08-22       Impact factor: 4.138

Review 3.  RNA interference: historical overview and significance.

Authors:  Mary K Montgomery
Journal:  Methods Mol Biol       Date:  2004

4.  NOCA-1 functions with γ-tubulin and in parallel to Patronin to assemble non-centrosomal microtubule arrays in C. elegans.

Authors:  Shaohe Wang; Di Wu; Sophie Quintin; Rebecca A Green; Dhanya K Cheerambathur; Stacy D Ochoa; Arshad Desai; Karen Oegema
Journal:  Elife       Date:  2015-09-15       Impact factor: 8.140

Review 5.  Creation of transgenic lines using microparticle bombardment methods.

Authors:  Vida Praitis
Journal:  Methods Mol Biol       Date:  2006

6.  Auxin-mediated Protein Degradation in Caenorhabditis elegans.

Authors:  Michael A Q Martinez; David Q Matus
Journal:  Bio Protoc       Date:  2020-04-20

7.  Expression and imaging of fluorescent proteins in the C. elegans gonad and early embryo.

Authors:  Rebecca A Green; Anjon Audhya; Andrei Pozniakovsky; Alexander Dammermann; Hayley Pemble; Joost Monen; Nathan Portier; Anthony Hyman; Arshad Desai; Karen Oegema
Journal:  Methods Cell Biol       Date:  2008       Impact factor: 1.441

8.  Methods for Rapid Protein Depletion in C. elegans using Auxin-Inducible Degradation.

Authors:  Nikita S Divekar; Hannah E Horton; Sarah M Wignall
Journal:  Curr Protoc       Date:  2021-02

9.  Kinetochore-independent chromosome segregation driven by lateral microtubule bundles.

Authors:  Christina C Muscat; Keila M Torre-Santiago; Michael V Tran; James A Powers; Sarah M Wignall
Journal:  Elife       Date:  2015-05-30       Impact factor: 8.140

10.  The auxin-inducible degradation (AID) system enables versatile conditional protein depletion in C. elegans.

Authors:  Liangyu Zhang; Jordan D Ward; Ze Cheng; Abby F Dernburg
Journal:  Development       Date:  2015-11-09       Impact factor: 6.868

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  2 in total

1.  Multiple motors cooperate to establish and maintain acentrosomal spindle bipolarity in C. elegans oocyte meiosis.

Authors:  Gabriel Cavin-Meza; Michelle M Kwan; Sarah M Wignall
Journal:  Elife       Date:  2022-02-11       Impact factor: 8.713

2.  Zinc transporters ZIPT-2.4 and ZIPT-15 are required for normal C. elegans fecundity.

Authors:  Aaron C Sue; Sarah M Wignall; Teresa K Woodruff; Thomas V O'Halloran
Journal:  J Assist Reprod Genet       Date:  2022-05-01       Impact factor: 3.357

  2 in total

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