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On the nature of in vivo requirements for rde-4 in RNAi and developmental pathways in C. elegans.


ABSTRACT: C. elegans RDE-4 is a double-stranded RNA binding protein that has been shown to play a key role in response to foreign double-stranded RNA (dsRNA). We have used diverse tools for analysis of gene function to characterize the domain and organismal foci of RDE-4 action in C. elegans. First, we examined the focus of activity within the RDE-4 protein, by testing a series of RDE-4 deletion constructs for their ability to support dsRNA-triggered gene silencing. These assays indicated a molecular requirement for a linker region and the second dsRNA-binding domain of RDE-4, with ancillary contributions to function from the C and N terminal domains. Second, we used mosaic analysis to explore the cellular focus of action of RDE-4. These experiments indicated an ability of RDE-4 to function non-autonomously in foreign RNA responses. Third, we used growth under stressful conditions to search for evidence of an organismal focus of action for RDE-4 distinct from its role in response to foreign dsRNA. Propagation at high temperatures exposed a conditional requirement for RDE-4 for optimal growth and fertility, indicating at least under these conditions that RDE-4 can serve an essential role in C. elegans.

SUBMITTER: Blanchard D 

PROVIDER: S-EPMC3218512 | biostudies-literature | 2011 May-Jun

REPOSITORIES: biostudies-literature

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On the nature of in vivo requirements for rde-4 in RNAi and developmental pathways in C. elegans.

Blanchard Daniel D   Parameswaran Poornima P   Lopez-Molina Javier J   Gent Jonathan J   Saynuk Jamie Fleenor JF   Fire Andrew A  

RNA biology 20110501 3


C. elegans RDE-4 is a double-stranded RNA binding protein that has been shown to play a key role in response to foreign double-stranded RNA (dsRNA). We have used diverse tools for analysis of gene function to characterize the domain and organismal foci of RDE-4 action in C. elegans. First, we examined the focus of activity within the RDE-4 protein, by testing a series of RDE-4 deletion constructs for their ability to support dsRNA-triggered gene silencing. These assays indicated a molecular requ  ...[more]

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