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Series GSE83316 Query DataSets for GSE83316
Status Public on Apr 05, 2017
Title Natural variation of piRNA expression affects immunity to transposable elements
Organism Drosophila melanogaster
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary In the Drosophila germline, transposable elements (TEs) are silenced by PIWI-interacting RNA (piRNA) that originate from distinct genomic regions termed piRNA clusters and are processed by PIWI-subfamily Argonaute proteins. Here, we explore the variation in the ability to restrain an alien TE in different Drosophila strains. The I-element is a retrotransposon involved in the phenomenon of I-R hybrid dysgenesis in Drosophila melanogaster. Genomes of R strains do not contain active I-elements, but harbour remnants of ancestral I-related elements. The permissivity to I-element activity of R females, called reactivity, varies considerably in natural R populations, indicating the existence of a strong natural polymorphism in defense systems targeting transposons. To reveal the nature of such polymorphisms, we compared ovarian small RNAs between R strains with low and high reactivity and show that reactivity negatively correlates with the ancestral I-element-specific piRNA content. Analysis of piRNA clusters containing remnants of I-elements shows increased expression of the piRNA precursors and enrichment by the Heterochromatin Protein 1 homolog, Rhino, in weak R strains, which is in accordance with stronger piRNA expression by these regions. To explore the nature of the differences in piRNA production, we focused on two R strains, weak and strong, and showed that the efficiency of maternal inheritance of piRNAs as well as the I-element copy number are very similar in both strains. At the same time, germline and somatic uni-strand piRNA clusters generate more piRNAs in strains with low reactivity, suggesting the relationship between the efficiency of primary piRNA production and variable response to TE invasions. The strength of adaptive genome defense is likely driven by naturally occurring polymorphisms in the rapidly evolving piRNA pathway proteins. We hypothesize that hyper-efficient piRNA production is contributing to elimination of a telomeric retrotransposon HeT-A, which we have observed in one particular transposon-resistant R strain.
 
Overall design The fractions of small RNAs (19-29 nt) from ovaries of four R strains of Drosophila melanogaster, and from embryos of two R strains of Drosophila melanogaster, were sequenced using Illumina HiSeq 2000.
 
Contributor(s) Ryazansky S, Radion E, Mironova A, Akulenko N, Abramov Y, Morgunova V, Kordyukova M, Olovnikov I, Kalmykova A
Citation(s) 28448516
Submission date Jun 13, 2016
Last update date May 15, 2019
Contact name Sergei Ryazansky
E-mail(s) s.ryazansky@gmail.com
Phone +7-499-196-81-73
Organization name Institute of Molecular Genetics
Department Department of Molecular Genetics of Cell
Street address Kurchatov sq., 2
City Moscow
ZIP/Postal code 123182
Country Russia
 
Platforms (1)
GPL13304 Illumina HiSeq 2000 (Drosophila melanogaster)
Samples (7)
GSM2199449 Small RNAs from ovaries of Paris R strain
GSM2199450 Small RNAs from ovaries of Misy R strain
GSM2199451 Small RNAs from ovaries of cn bw; e R strain
Relations
BioProject PRJNA325554
SRA SRP076499

Download family Format
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Supplementary file Size Download File type/resource
GSE83316_RAW.tar 128.8 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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