Literature DB >> 26832686

RNAi-Mediated Inactivation of Autophagy Genes in Caenorhabditis elegans.

Nicholas J Palmisano1, Alicia Meléndez1.   

Abstract

RNA interference (RNAi) is a process that results in the sequence-specific silencing of endogenous mRNA through the introduction of double-stranded RNA (dsRNA). In the nematode Caenorhabditis elegans, RNA inactivation can be used at any specific developmental stage or during adulthood to inhibit a given target gene. Investigators can take advantage of the fact that, in C. elegans, RNAi is unusual in that it is systemic, meaning that dsRNA can spread throughout the animal and can affect virtually all tissues except neurons. Here, we describe a protocol for the most common method to achieve RNAi in C. elegans, which is to feed them bacteria that express dsRNA complementary to a specific target gene. This method has various advantages, including the availability of libraries that essentially cover the whole genome, the ability to treat animals at any developmental stage, and that it is relatively cost effective. We also discuss how RNAi specific to autophagy genes has proven to be an excellent method to study the role of these genes in autophagy, as well as other cellular and developmental processes, while also highlighting the caveats that must be applied.
© 2016 Cold Spring Harbor Laboratory Press.

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Year:  2016        PMID: 26832686      PMCID: PMC8103221          DOI: 10.1101/pdb.prot086520

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  30 in total

1.  ALIS are stress-induced protein storage compartments for substrates of the proteasome and autophagy.

Authors:  Jason Szeto; Natalia A Kaniuk; Veronica Canadien; Rozalia Nisman; Noboru Mizushima; Tamotsu Yoshimori; David P Bazett-Jones; John H Brumell
Journal:  Autophagy       Date:  2006-07-22       Impact factor: 16.016

2.  Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans.

Authors:  A Fire; S Xu; M K Montgomery; S A Kostas; S E Driver; C C Mello
Journal:  Nature       Date:  1998-02-19       Impact factor: 49.962

3.  On the role of RNA amplification in dsRNA-triggered gene silencing.

Authors:  T Sijen; J Fleenor; F Simmer; K L Thijssen; S Parrish; L Timmons; R H Plasterk; A Fire
Journal:  Cell       Date:  2001-11-16       Impact factor: 41.582

4.  Detection of Autophagy in Caenorhabditis elegans Using GFP::LGG-1 as an Autophagy Marker.

Authors:  Nicholas J Palmisano; Alicia Meléndez
Journal:  Cold Spring Harb Protoc       Date:  2016-01-04

5.  Detecting Autophagy in Caenorhabditis elegans Embryos Using Markers of P Granule Degradation.

Authors:  Nicholas J Palmisano; Alicia Meléndez
Journal:  Cold Spring Harb Protoc       Date:  2016-01-04

6.  Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans.

Authors:  L Timmons; D L Court; A Fire
Journal:  Gene       Date:  2001-01-24       Impact factor: 3.688

7.  Autophagy and lipid metabolism coordinately modulate life span in germline-less C. elegans.

Authors:  Louis R Lapierre; Sara Gelino; Alicia Meléndez; Malene Hansen
Journal:  Curr Biol       Date:  2011-09-08       Impact factor: 10.834

8.  Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library.

Authors:  Jean-François Rual; Julian Ceron; John Koreth; Tong Hao; Anne-Sophie Nicot; Tomoko Hirozane-Kishikawa; Jean Vandenhaute; Stuart H Orkin; David E Hill; Sander van den Heuvel; Marc Vidal
Journal:  Genome Res       Date:  2004-10       Impact factor: 9.043

9.  Loss of the putative RNA-directed RNA polymerase RRF-3 makes C. elegans hypersensitive to RNAi.

Authors:  Femke Simmer; Marcel Tijsterman; Susan Parrish; Sandhya P Koushika; Michael L Nonet; Andrew Fire; Julie Ahringer; Ronald H A Plasterk
Journal:  Curr Biol       Date:  2002-08-06       Impact factor: 10.834

10.  Loss of LIN-35, the Caenorhabditis elegans ortholog of the tumor suppressor p105Rb, results in enhanced RNA interference.

Authors:  Ben Lehner; Andrea Calixto; Catriona Crombie; Julia Tischler; Angelo Fortunato; Martin Chalfie; Andrew G Fraser
Journal:  Genome Biol       Date:  2006-01-20       Impact factor: 13.583

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