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Status |
Public on Sep 01, 2012 |
Title |
C. elegans piRNAs mediate the genome-wide surveillance of germline transcripts |
Organism |
Caenorhabditis elegans |
Experiment type |
Non-coding RNA profiling by high throughput sequencing
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Summary |
Piwi Argonautes and Piwi-interacting RNAs (piRNAs) mediate genome defense by targeting transposons. However, many piRNA species lack obvious sequence complementarity to transposons or other loci. For example, only one C. elegans transposon is a known piRNA target. Here we show that, in mutants lacking the Piwi Argonaute PRG-1 and associated piRNAs (21U-RNAs), many silent loci in the germline exhibit increased levels of mRNA expression and depletion of an amplified RNAdependent RNA polymerase (RdRP)-derived species of small RNA termed 22G-RNAs. Sequences depleted of 22G-RNAs are enriched nearby potential target sites that base pair imperfectly but extensively to 21U-RNAs. We show that PRG-1 is required to initiate, but not to maintain, silencing of transgenes engineered to contain complementarity to endogenous 21U-RNAs. Our findings support a model in which C. elegans piRNAs utilize their enormous repertoire of targeting capacity to scan the germline transcriptome for foreign sequences, while endogenous germline-expressed genes are actively protected from piRNA-induced silencing.
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Overall design |
Examine small RNA population changes in prg-1 and rescued strains
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Contributor(s) |
Lee H, Gu W |
Citation(s) |
22738724, 29456136 |
Submission date |
Jun 14, 2012 |
Last update date |
Jul 26, 2019 |
Contact name |
Craig Mello |
Organization name |
University of Massachusetts Medical School
|
Department |
Program in Molecular Medicine
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Lab |
Craig Mello
|
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 (6)
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Relations |
BioProject |
PRJNA168500 |
SRA |
SRP013749 |