Published January 2012 | Version Published + Supplemental Material
Journal Article Open

Production of artificial piRNAs in flies and mice

Abstract

In animals a discrete class of small RNAs, the piwi-interacting RNAs (piRNAs), guard germ cell genomes against the activity of mobile genetic elements. piRNAs are generated, via an unknown mechanism, from apparently single-stranded precursors that arise from discrete genomic loci, termed piRNA clusters. Presently, little is known about the signals that distinguish a locus as a source of piRNAs. It is also unknown how individual piRNAs are selected from long precursor transcripts. To address these questions, we inserted new artificial sequence information into piRNA clusters and introduced these marked clusters as transgenes into heterologous genomic positions in mice and flies. Profiling of piRNA from transgenic animals demonstrated that artificial sequences were incorporated into the piRNA repertoire. Transgenic piRNA clusters are functional in non-native genomic contexts in both mice and flies, indicating that the signals that define piRNA generative loci must lie within the clusters themselves rather than being implicit in their genomic position. Comparison of transgenic animals that carry insertions of the same artificial sequence into different ectopic piRNA-generating loci showed that both local and long-range sequence environments inform the generation of individual piRNAs from precursor transcripts.

Additional Information

© 2012 RNA Society. Published by Cold Spring Harbor Laboratory Press. Received August 8, 2011. Accepted September 26, 2011. Published in Advance November 17, 2011. We thank members of the Hannon and Aravin labs for helpful discussion and comments on the manuscript. We thank members of the McCombie lab (CSHL) and Igor Antoshechkin (Caltech) for help with RNA sequencing. We thank Andres Canela (CSHL) for technical assistance and Simon Knott (CSHL) and Alex Zahn (Caltech) for help with statistical analysis. Sang Yong Kim (CSHL) created the transgenic mice used in this study. F.M. was supported by the Volkswagen Foundation and B.C. by the Boehringer Ingelheim Fonds. This work was supported by grants from the National Institutes of Health (DP2 OD007371A and R00HD057233 to A.A.A.; 5R01GM062534 to G.J.H.), by the Ellison Medical Foundation (A.A.A.), and by a kind gift from Kathryn W. Davis (G.J.H.).

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Published - Muerdter2012p16789Rna.pdf

Supplemental Material - Muerdter_suppl_figures.pdf

Supplemental Material - Supp_Fig_Legends.docx

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Additional details

Identifiers

PMCID
PMC3261743
Eprint ID
28982
Resolver ID
CaltechAUTHORS:20120126-110548127

Funding

Volkswagen Foundation
Boehringer Ingelheim Fonds
NIH
DP2 OD007371A
NIH
R00 HD057233
NIH
5R01GM062534
Ellison Medical Foundation

Dates

Created
2012-01-26
Created from EPrint's datestamp field
Updated
2021-11-09
Created from EPrint's last_modified field