Literature DB >> 20359305

A modified feeding RNAi method for simultaneous knock-down of more than one gene in Caenorhabditis elegans.

Kyoengwoo Min1, Junsu Kang, Junho Lee.   

Abstract

RNA interference (RNAi) is a commonly used technique for reverse genetic approaches in Caenorhabditis elegans. Feeding RNAi is the most convenient and inexpensive method for performing genome-wide RNAi screens. However, it has been reported that knock-down of two genes (double RNAi) by feeding RNAi using a mixture of bacteria that each contained one dsRNA species produced poor results. To overcome this problem of inefficiency, we designed and tested a double feeding RNAi method using a single RNAi construct containing two gene fragments. From experiments with three different sets of genes, we found that the new double RNAi method consistently produced significantly enhanced double knock-down phenotypes. The double feeding RNAi approach described here provides a method to consistently examine phenotypes caused by depletion of more than one gene in C. elegans.

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Year:  2010        PMID: 20359305     DOI: 10.2144/000113365

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  15 in total

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6.  Proteins in aggregates functionally impact multiple neurodegenerative disease models by forming proteasome-blocking complexes.

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7.  A systematic analysis of protein palmitoylation in Caenorhabditis elegans.

Authors:  Matthew J Edmonds; Alan Morgan
Journal:  BMC Genomics       Date:  2014-10-02       Impact factor: 3.969

8.  Autophagy and modular restructuring of metabolism control germline tumor differentiation and proliferation in C. elegans.

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Journal:  Autophagy       Date:  2016-01-13       Impact factor: 16.016

9.  Using Multiple Phenotype Assays and Epistasis Testing to Enhance the Reliability of RNAi Screening and Identify Regulators of Muscle Protein Degradation.

Authors:  Susann Lehmann; Freya Shephard; Lewis A Jacobson; Nathaniel J Szewczyk
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10.  Knockdown of the C. elegans kinome identifies kinases required for normal protein homeostasis, mitochondrial network structure, and sarcomere structure in muscle.

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Journal:  Cell Commun Signal       Date:  2013-09-23       Impact factor: 5.712

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