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Status |
Public on Oct 01, 2009 |
Title |
High throughput sequencing of mutants in the WAGO pathway |
Organism |
Caenorhabditis elegans |
Experiment type |
Non-coding RNA profiling by high throughput sequencing Other
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Summary |
Diverse naturally-occurring small RNA species interact with Argonaute proteins to mediate sequence-specific regulation in animals. In addition to micro-RNAs (miRNAs), which collectively regulate thousands of target mRNAs, other endogenous small RNA species include the Piwi-associated piRNAs that are important for fertility and a less well-characterized class of small RNAs often referred to simply as endo-siRNAs. Here we have utilized deep-sequencing technology and C. elegans genetics to explore the biogenesis and function of endo-siRNAs. We describe conditional alleles of the dicer-related helicase, drh-3, that implicate DRH-3 in both the response to foreign dsRNA as well as the RNA-dependent RNA Polymerase (RdRP)-dependent biogenesis of a diverse class of endogenous small RNAs, termed 22G-RNAs. We show that 22G-RNAs are abundantly expressed in the germline and maternally inherited and are the products of at least two distinct 22G-RNA systems. One system is dependent on worm-specific AGOs, including WAGO-1, which localizes to germline nuage-related structures termed P-granules. The WAGO 22G-RNA system silences transposons, pseudogenes and cryptic loci as well as a number of genes. Finally, we demonstrate that components of the nonsense-mediated decay pathway function in at least one of the multiple, distinct WAGO surveillance pathways. These findings broaden our understanding of the biogenesis and diversity of 22G-RNA species and suggest potential novel regulatory functions for these small RNAs.
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Overall design |
18 samples examined. Small RNA libraries generated from: C. elegans animals with mutations in the WAGO pathway and a WAGO-1 immunopercipitate.
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Contributor(s) |
Gu W, Mello CC |
Citation(s) |
19800275, 29456136 |
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Submission date |
Sep 22, 2009 |
Last update date |
Jul 26, 2019 |
Contact name |
Craig Mello |
Organization name |
University of Massachusetts Medical School
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Department |
Program in Molecular Medicine
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Lab |
Craig Mello
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Street address |
368 Plantatoin Street, Suite AS5-2047
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City |
Worcester |
State/province |
MA |
ZIP/Postal code |
01605 |
Country |
USA |
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Platforms (1) |
GPL9269 |
Illumina Genome Analyzer II (Caenorhabditis elegans) |
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Samples (18)
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This SubSeries is part of SuperSeries: |
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Relations |
SRA |
SRP001449 |
BioProject |
PRJNA123493 |